AU4493099A - Directed combinatorial compound library and high throughput assays for screening same - Google Patents

Description

WO 99/64378 PCT/CA99/00550 -1l TITLE: DIRECTED COMBINATORIAL COMPOUND LIBRARY AND HIGH THROUGHPUT ASSAYS FOR SCREENING SAME FIELD OF THE INVENTION The invention is directed to predetermined libraries of compounds, related compounds useful 5 for making such libraries, and compositions containing the compounds. BACKGROUND OF THE INVENTION Interactions between proteins and carbohydrates are involved in a wide array of biological recognition events, including fertilization, molecular targeting, intercellular recognition, and viral, bacterial, and fungal pathogenesis. The oligosaccharide portions of glycoproteins and glycolipids 10 mediate recognition between cells and cells, between cells and ligands, between cells and the extracellular matrix, and between cells and pathogens. Inhibition of carbohydrate processing enzymes involved in the synthesis, transport, and cleavage of oligosaccharides can be used as a means to inhibit interactions between proteins and oligosaccharides and inhibit the recognition phenomena. In particular, two groups of enzymes 15 associated with the in vivo synthesis of oligosaccharides can be targeted. The enzymes of the Leloir pathway transfer sugars activated as sugar nucleoside phosphates to a growing oligosaccharide chain. The nucleoside phosphate building blocks involved in the Leloir pathway include: UDP-Glc, UDP GlcUA, UDP-GlcNAc, UDP-Gal, UDP-GaINAc, UDP-Idua, GDP-Man, GDP-Fuc, and CMP-NeuAc. The other group of enzymes associated with the in vivo synthesis of oligosaccharides are the non-Leloir 20 pathway enzymes that transfer carbohydrate units activated as sugar phosphates, but not as sugar nucleoside phosphates. Glycosyltransferases catalyze the addition of activated sugars from nucleotides in a stepwise fashion to a protein or lipid or to the non-reducing end of a growing oligosaccharide. There are estimated to be over 200 glycosyltransferases encoded by mammalian cells, many of which appear to 25 be developmentally regulated, resulting in tissue specific-patterns of glycosylation (Schachter, H. Curr.Opin.Struct.Biol. 1:755-765, 1991; and Paulson, J.C. and Colley, K.J. J.Biol.Chem. 264:17615 17618, 1989). Each NDP-sugar residue requires a distinct class of glycosyltransferase and each of the glycosyltransferases appear to catalyze the formation of a unique glycosidic linkage. Oligosaccharides may be linked to proteins by N-glycosidic or 0-glycosidic linkages. In an N-linkage, an N-acetyl 30 glucosamine residue is p-linked to the amide nitrogen of an Asn in the sequence Asn-X-Ser or Asn-X Thr (X is any amino acid). In an 0-linkage, the disaccharide P-galactosyl-(1,3)-alpha-N acetylgalactosamine is alpha-linked to the hydroxyl group of serine or threonine. The Golgi enzymes 1(T1-6) N-acetylglucosaminyltransferase V (i.e. GlcNAc-TV) and core 2 P(T1-6) N-acetylglucosaminyltransferase (i.e. core 2 GlcNAc-T) are responsible for the extension of 35 GIcNAc P(TI-6) branched N- and 0-linked carbohydrate side chains of cell-surface glycoproteins. These side chains are found on the surface of human tumor cells and they have been associated with cancer invasion and metastasis (Dennis et. al., Science 236: 582, 1987; Demetriou et. aL., J Cell Biol. 130:383, 1995). GlcNAc-TV and core 2 GIcNAc-T have been shown to be up-regulated in human carcinomas (Fernandes et al., Cancer Res. 51:718-723, 1991; Shimodaira, K. et al, Cancer Research WO 99/64378 PCT/CA99/00550 57:5201, 1997), a phenomenon that has been associated with the activation of the ras signaling pathway (Dennis et al.. Science 236:582-585, 1987; Dennis et al Oncogene 4:853-860, 1989)). Overexpression of GIcNAc-TV in epithelial cells has been found to result in morphological transformation and tumor formation in mice (Demetriou et al, J. Cell Biol. 130:383-392, 1995). 5 Therefore. GIcNAc-TV as well as enzymes supplying acceptor substrates to GIcNAc-TV (i.e. GlcNAc-TI. c-mannosidase 11 and core 2 GIcNAc-T of the 0-linked pathway) are useful targets for anti-cancer pharmaceuticals. Fucosyltransferases are involved in determining the expression of sialyl Lewis' (sLex ) antigen on the surface of blood cells. In the inflammatory process, selectin-sLexx mediated attachment 10 of leukocytes is a key step for leukocyte activation and trans-endothelial migration. Inhibition of fuscosyltransferases responsible for the synthesis of sLexx will prevent the formation of selectin carbohydrate complexes and therefore will interfere with the first step of the inflammatory process. Inhibitors would be useful for the treatment of chronic inflammatory disorders such as asthma, rheumatoid arthritis, inflammatory bowel disease and atherosclerosis. All of these disorders are 15 conditions where an inappropriate inflammatory response is involved and suppression is desirable. Blocking of certain enzymes in the carbohydrate processing pathway leads to an increased sensitivity of immune cells to Th 1 cytokines (interferon and interleukin-2), thereby further promoting the Thl immune response. While interferon-alpha itself has anti-viral activity, it appears to be insufficient on its own in eliminating chronic infections such as hepatitis. Therefore, enzyme inhibitors 20 can be used to enhance the effect of Th l cytokines in the treatment of many viral, bacterial, fungal and parasitic infections, including hepatitis B and C. Inhibitors of enzymes that synthesize specific carbohydrate structures of bacteria that play an important role in pathogenicity can be used to enhance the susceptibility of the bacteria to the host immune system and to inhibit the entry of the bacteria into human cells and tissues. For example, a 25 specific bacterial carbohydrate structure called low molecular weight oligosaccharide (LOS) that is similar to a carbohydrate structure found on human glycoproteins and glycolipids, protects the bacterium from being recognized and cleared by the host's immune system. Inhibitors of the enzymes responsible for synthesizing the LOS structure can reduce the ability of bacteria such as N. gonorrhea to elude immune surveillance in a host. 30 It is apparent that there is a need for small molecule inhibitors of carbohydrate processing enzymes including GIcNAc-transferases I through V, galactosyltransferases, sialo transferases, fucosyl transferases. and core 2 GlcNAc, with structural and conformational diversity. There is also a need for high throughput methods for screening the inhibitors to identify "lead" pharmaceutical compounds. SUMMARY OF THE INVENTION 35 The present invention utilizes a combinatorial chemistry approach. Combinatorial chemistry generally involves linking together, in step-wise fashion, identical or non-identical building blocks typically referred to as "monomeric units", or "chemical groups". Using this approach, the present inventors developed combinatorial libraries of small molecule inhibitors of carbohydrate processing WO 99/64378 PCT/CA99/00550 enzymes that transfer a sugar from a specific sugar nucleotide donor to a specific acceptor. The small molecule inhibitors have structural and conformational diversity. Enzymes that may be inhibited by the small molecule inhibitors include eukaryotic and procaryotic glycosyltransferases. The molecules can be screened using high throughput methods enabling identification of lead pharmaceutical compounds. 5 Broadly stated the present invention relates to a combinatorial library comprising a predetermined collection of nucleoside peptide molecules for inhibiting the transfer of a sugar from a selected sugar nucleotide donor to a selected acceptor by a carbohydrate processing enzyme wherein a nucleoside peptide molecule comprises (a) a nucleoside monomer; (b) a spacer monomer coupled to the nucleoside monomer wherein the spacer monomer comprises one or more amino acids, or a 10 peptidomimetic or peptide analog; and (c) cap monomers attached to the spacer monomer; wherein the nucleoside peptide molecules differ from each other as to the identity of at least one element of the nucleoside monomer, spacer monomer or cap monomer. In addition, a nucleoside peptide molecule is contemplated comprising (a) a nucleoside monomer; (b) a spacer monomer coupled to a nucleoside monomer, wherein the spacer monomer 15 comprises one or more amino acids, or a peptidomimetic or peptide analog; and (c) cap monomers attached to the spacer monomer. The invention also relates to a process for preparing a combinatorial library containing a predetermined collection of nucleoside peptide molecules for inhibiting the transfer of a sugar from a selected sugar nucleotide donor having a heterocyclic amine base, to a selected acceptor by a 20 carbohydrate processing enzyme comprising: (a) coupling one or more amino acids or a peptidomimetic or peptide analog, to a nucleoside monomer unit which nucleoside monomer unit comprises a heterocyclic amine base coupled to a sugar wherein the base corresponds to the heterocyclic amine base of the sugar nucleotide donor, or a modified form or analogue of the base: and 25 (b) capping any free functional groups or amine groups with a cap monomer unit. The invention also relates to methods of using the combinatorial library for screening for pharmacologically active molecules: and pharmaceutical compositions containing compounds identified by the methods. Further, the invention contemplates a solid-phase bioassay for identifying a compound having 30 inhibitory activity against a carbohydrate processing enzyme which comprises (a) coupling an acceptor for the carbohydrate processing enzyme to a polymer and coating onto a carrier; (b) adding a carbohydrate processing enzyme, a sugar nucleotide donor labeled with a detectable substance, and a test compound; and (c) measuring the detectable change produced by the detectable substance. The invention also contemplates a method for identifying a compound that inhibits N-linked 35 oligosaccharide processing comprising (a) reacting a test compound with cells expressing N-linked oligosaccharides, in the presence of leukoagglutinating phytohemagglutinin (L-PHA) and measuring alkaline phosphatase activity; and (b) comparing to a control in the absence of the compound wherein an increase in alkaline phosphatase activity indicates that the compound inhibits N-linked oligosaccharide processing. The method may be used to identify compounds that inhibit all steps in the WO 99/64378 PCT/CA99/00550 -4 N-linked oligosaccharide pathway prior to 31-4 Gal-transferase, including compounds that inhibit the carbohydrate processing enzymes specifically described herein, and Golgi a-mannosidase. A compound contemplated by the present invention having inhibitory activity against a carbohydrate processing enzyme can be useful for the treatment and prophylaxis of tumor growth and 5 metastasis of tumors: the prevention of tumor recurrence after surgery; the treatment of other anti proliferative conditions such as viral infections; the stimulation of bone marrow cell proliferation, the treatment of immunocompromised patients, such as patients infected with HIV, or other viruses or infectious agents including bacteria and fungi; the prevention and treatment of diseases caused by bacterial pathogens having carbohydrate structures on their surface associated with virulence such as 10 Neisseria. Haemophilus, E. coli, Bacillus, Salmonella, Campylobacter, Klebsiella. Pseudomonas, Streptococcus, Chlamydia, Borrelia, Coxiella, Helicobacter, and Mycobacterim species; or, the treatment of inflammatory disorders such as asthma, rheumatoid arthritis, inflammatory bowel disease, and atherosclerosis. A compound of the invention may also be used in patients undergoing bone marrow transplants, and as hemorestorative or chemoprotective agents in patients with chemical or 15 tumor-induced immune suppression. Other objects. features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples while indicating preferred embodiments of the invention are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention 20 will become apparent to those skilled in the art from this detailed description. BRIEF DESCRIPTION OF THE DRAWINGS The invention will now be described in relation to the drawings in which: Figure 1 is a schematic diagram showing a process for preparing 2.3-O-isopropylidineuridine from uridine: 25 Figure 2 is a schematic diagram showing a process for preparing 2,3-0-isopropylidene-5-0 methane sulfonyl uridine from 2,3-0-isopropylidine uridine; Figure 3 is a schematic diagram showing a process for preparing 5-deoxy-5-azido-2,3-0 isopropylidenyl uridine from 2,3-O-isopropylidene-5-O-methanesulfonyl uridine; Figure 4 is a schematic diagram showing a process for preparing 5-deoxy-5-amino-2,3-0 30 isopropylidenyl uridine from the parent azide; Figure 5 is a schematic diagram showing a process for coupling an N-Boc protected spacer monomer unit to a nucleoside monomer unit; Figure 6 is a schematic diagram for a process for deprotecting an N-Boc protected spacer monomer unit coupled to a nucleoside monomer unit; 35 Figure 7 is a schematic diagram showing a process for repeated coupling of Fmoc -protected spacer monomer units to a nucleoside monomer unit; Figure 8 is a schematic diagram for capping a spacer monomer unit that is coupled to a nucleoside monomer unit; WO 99/64378 PCT/CA99/00550 -5 Figure 9 is a schematic diagram showing the synthesis of a glycopolymer for a solid-phase core 2 GlcNAc-T assay; Figure 10 is a schematic diagram showing a glycopolymer for a solid-phase GlcNAc-T V assay; 5 Figure I I is a graph showing the distribution of normalized core 2 GlcNAc-T assay results for 1600 assays expressed as % control; and Figure 12 is a graph showing the results of a high-throughput screen to detect microbial extracts with inhibitory effects on N-linked oligosaccharide processing in MDAY-D2 cells. DETAILED DESCRIPTION OF THE INVENTION 10 Nucleoside Peptide Molecules As used herein "monomer unit" refers to a molecule prior to coupling or conjugation to another monomer unit. A "monomer" refers to a molecule after coupling or conjugating to form a nucleoside peptide molecule. Monomer units used in the present invention to form the predetermined nucleoside peptide molecules include a nucleoside monomer unit, a spacer monomer unit, and a cap 15 monomer unit. A nucleoside monomer unit is selected based on the type of carbohydrate processing enzyme targeted for inhibition, and in particular the sugar nucleotide donor for the enzyme from which a sugar is transferred to an acceptor. A "sugar nucleotide donor" refers to a molecule comprising a nucleotide having a sugar component, a heterocyclic amine base, and a phosphate unit, coupled to a selected sugar 20 that is transferred by a carbohydrate processing enzyme to an acceptor. An "acceptor" refers to the part of a carbohydrate structure (e.g. glycoprotein, glycolipid) where the selected sugar is transferred by a carbohydrate processing enzyme. Carbohydrate processing enzymes for which combinatorial libraries may be prepared in accordance with the invention include eukaryotic glycosyltransferases involved in the biosynthesis of 25 glycoproteins, glycolipids, glycosylphosphatidylinositols and other complex glycoconjugates, and prokaryotic glycosyltransferases involved in the synthesis of carbohydrate structures of bacteria and viruses, including enzymes involved in LOS and lipopolysaccharide biosynthesis. Examples of enzymes include glycosyltransferases such as N-acetylglucosaminyltransferases, including N acetylglucosaminyltransferases I through V and p-1,3-galactosyl-O-glycosyl-glycoprotein P 1,6-N 30 acetylgucosaminyl transferase (core 2 GIcNAc); fucosyltransferase; N-acetyl galactosaminyltransferases; galactosyltransferases; mannosyltransferases; and glucuronosyltransferases, preferably N-acetylglucosaminyltransferases. Table 1 provides examples of eukaryotic carbohydrate processing enzymes, and their sugar nucleotide donors and acceptors. Table 2 provides a list of prokaryotic carbohydrate processing enzymes. 35 A nucleoside monomer unit used in the molecules of the present invention is composed of a heterocyclic amine base in P-N-glycosidic linkage with a sugar. Generally, the sugar is ribose, or deoxyribose, and the heterocyclic amine base corresponds to the heterocyclic amine base of the sugar nucleotide donor for a selected carbohydrate processing enzyme. For example, uracil can be selected WO 99/64378 PCT/CA99/00550 -6 for N-acetylglucosaminyltransferases and galactosyltransferases: cvtosine for asialo transferases, and guanine for fucosyltransferases. Structural analogues of the heterocyclic amine bases may also be used. For example, when the base is uracil it may have groups at the C-5 position including but not limited to alkyl or aryl with 5 electron donating and electron withdrawing groups. Hydroxyl groups in the base may also be protected. The sugar may be modified for example, the 2' and 3' hydroxyls may be blocked with acetonide, acylated. or alkylated or substituted with other groups such as halogen. Specific examples of nucleoside monomer units include uridine, 2'-deoxyuridine, and 5' amino-5'-deoxy-2',3'-O-isopropylidine uridine (for galactosyltransferases and GlcNAc transferases, 10 cytidine, 2'-deoxycytidine, 5'-amino-5'-deoxy-2',3'-O-isopropylidinecytidine (for sialo transferases), and guanosine, 2'-deoxyguanosine, 5'-amino-5'-deoxy-2',3'-O-isopropylidineguanosine (for fucosyl transferases), respectively. A nucleoside monomer unit is linked to a spacer monomer unit by coupling appropriate reactive groups such as carboxylic acids, or activated esters thereof (e.g. hydroxybenzotriazole, 15 pentafluorophenol or N-hydroxysuccinimide esters), carboxylic anhydrides (mixed or symmetric), acyl halides, chloroformates, halides, ketones. aldehydes, sulfonyl chlorides, isocyanates, or isothiocyanates, to other reactive functional groups such as amines to form a stable linkage such as an amide, carbamate, amino, sulfonamide, urea, or isourea, preferably an amide linkage. Each of the monomer units may have one or more identical or different reactive groups. 20 A spacer monomer unit for use in the invention may comprise any functional group that mimics the phosphate/sugar linkage in a sugar nucleotide donor for a carbohydrate processing enzyme, or which interacts with the enzyme by other mechanisms. The spacer monomer unit may have a charged center. Examples of spacer monomer units that can be used in the molecules of the invention include one or more amino acids, preferably a single amino acid, a dipeptide, or tripeptide, or 25 peptidomimetics/ peptide analog. Amino acids used in the spacer monomer unit may be naturally-occurring or synthetic amino acids, and they can be aliphatic, or aromatic. An amino acid in the spacer monomer unit may be a chiral or achiral amino acid including but not limited to an L-amino acid, a D-amino acid, an a-amino acid, a p-amino acid, or an analog of an amino acid. In addition, one or more amino acids in the spacer 30 monomer unit may be substituted with a substituent group such as an amide, alkyl, amine, halogen, ether, heterocycle, or an acidic group such as -COOH, or SO3H. The amino acids may be capped with suitable protecting groups as described herein. The amino acid or peptides may comprise acidic amino acid residues including aspartic acid or glutamic acid, and aspartic acid and glutamic acid mono-benzyl esters or t-butyl esters (for example, at the a- and P- positions for the former, and a- and y- for the 35 latter). Examples of amino acids that may be used in the spacer monomer unit include L-aspartic acid-a-benzyl ester, L-glutamic acid-y-benzyl ester. D-aspartic acid-P-benzyl ester, L-aspartic acid-p benzyl ester, L-glutamic acid-a-benzyl ester, L-tryptophan. 6-aminohexanoic acid. L-valine, m-tosyl L-histidine. L-leucine, p-methoxy-benzyl-L-cysteine, sarcosine, L-isoleucine, L-asparagine. o-p-tosyl WO 99/64378 PCT/CA99/00550 -7 L-arginine. o-nitro-L-arginine, N-E-CBz-L-lysine, L-glutamine. L-alanine, O-benzvl-L-threonine, 0 benzyl-L-tyrosine, L-methionine, 0-benzyl-L-serine, L-proline, L-phenylalanine. 3-alanine, a aminoisobutyric acid, homoarginine, homoproline, homoserine, norarginine, norleucine, ornthine, and p-nitrophenylalanine. 5 Peptidomimetics or peptide analogs may also be used in the spacer monomer unit. Generally, peptidomimetics are structurally similar to a paradigm, such as naturally-occuring peptides, but have one or more peptide linkages optionally replaced for example, by a linkage selected from the group consisting of: -CH2NH-, -CH2S-, CH2CH2- , -CH=CH- (cis and trans), -COCH2 -, -CH(OH) CH2-, and -CH2SO- by methods known in the art and further described in the following references: Spatola, 10 A. F. in CHEMISTRY AND BIOCHEMISTRY OF AMINO ACIDS, PEPTIDES, AND PROTEINS, B. Weinstein. eds., Marcel Dekker, New York, p.

2 6 7 (1983); Spatola, A. F., Vega Data (March 1983), Vol. 1, Issue 3, PEPTIDE BACKBONE MODIFICATIONS (general review); Morley. Trends Pharm Sci (1980) pp. 463-468 (general review): Gaute (1994) Angew. Chem., Int. Ed. Engl., 33:1699-1720; Giannis and Kolter (1993), Angew. Chem., Int. Ed. Engl., 32: 1244-1267; Hudson. D. et al., (1979) Int 15 J Pept Prot Res 14:177-185 (--CH2NH--, CH2CH 2 --); Spatola et al., (1986) Life Sci 38:1243-1249 (- CH2--S); Hann (1982) J. Chem. Soc. Perkin Trans. 1 307-314 (-CH=CH-, cis and trans); Almquist et al., (1980) J Med Chem 23:1392-1398 (-COCH 2 -); Jennings-White et al., (1982) Tetrahedron Lett 23:2533 (-COCH 2 -); Szelke et al., (1982) European Appin. EP 45665 CA: 97:39405 (1982) (-CH(OH) CH2-); Holladay et al., (1983) Tetrahedron Lett 24:4401-4404 (-C(OH)CH-2-); and Hruby (1982) Life 20 Sci 31:189-199 (-CH2-S-); each of which is incorporated herein by reference. Peptidomimetics or peptide analogs also include peptides wherein the N-terminus is derivatized for example to a -NXX 1 group, to a --NXC(O)X group, to a --NXC(O)OX group, to a --NXS(O) 2 X group, to a --NHC(O)NHX group where X and X, are hydrogen or lower alkyl with the proviso that X and X, are not both hydrogen, to a succinimide group, to a benzvloxycarbonyl-NH--(CBZ--NH--) group, to a 25 benzyloxycarbonyl-NH--group having from 1 to 3 substituents on the phenyl ring selected from the group consisting of lower alkyl, lower alkoxy, chloro, and bromo, peptides wherein the C terminus is derivatized to --C(O)X 2 where X 2 is selected from the group consisting of lower alkoxy, and --NX 3

X

4 where X 3 and X 4 are independently selected from the group consisting of hydrogen and lower alkyl. Free functional groups on a nucleoside peptide molecule, in particular free amine groups in 30 the spacer monomer, may be capped using the same or different chemical reactive groups used for a spacer monomer unit coupling to nucleoside monomer units. Examples of cap monomer units include ureas, thioureas, carbamates. and amide residues, which may be part of aromatic rings, non-aromatic rings, heterocyclics, carbocyclics, or fused ring systems. Reactive derivatives of naturally occurring alkaloids such as swainsonine or castanospermine may also be used as cap monomers. Examples of 35 commercially available reagents that may be used to form the cap monomer units include: benzoyl chloride, benzenesulfonyl isocyanate, 4-toluenesulfonyl isocyanate, 2-furonyl chloride, (R)-a methylbenzyl isocyanate, 4-(trifluoromethylthio)phenyl isocyanate, 2-methoxycarbonyl, phenyl isocyanate, 4-morpholine carbonyl chloride, I -isothiocyanato-4-(trans-4-octvlcyclohexyl) benezene, 3- WO 99/64378 PCT/CA99/00550 -8 (trifluoromethyl)phenyl isocyanate, I -adamantanecarbonyl chloride, 4-chlorobenezene sulfonyl isocyanate, quinoxay chloride, 2-thiophenecarbonyl chloride, 2-naphthyl isocyanate, 2-thiopheneacetyl chloride, 1-adamantyl isocyanate, 3-cyclopentylpropionyl chloride, pyrolidine carbonyl chloride, 4 trifluoromethoxy-benzoyl chloride, 3-methoxy benzoyl chloride, 4-[4-isothiocyanato phenyl azo] N,N 5 dimethyl aniline, chloro acetic anhydride, 4-fluoro benzoyl isocyanate, picolinic acid, nicotinic acid, isonicotinic acid, 6-methylnicotinic acid, 3-pydidylacetic acid, trans-3-(3-pyridyl)acrylic acid, (4 pyridylthio)acetic acid, 2-chloronicotinic acid, 6-chloronicotinic acid, 5,6-dichloronicotine acid, 6 hydroxypicolinic acid, 6-hydroxynicotinic acid, 3-hydroxypicolinic acid, 5-chloro-6-hydroxynicotinic acid, 4-pyridoxic, citrazinic acid, 2-furoic acid, 3-furoic acid, 5-bromo-2-furoic acid, 2 10 thiophenecarboxylic acid, 3-thiophenecarboxylic acid, 4-nitro-3-pyrazolecarboxylic acid, 5-nitro-3 pyrazolecarboxylic acid, 4 -hydroxy-7-fluoromethyl-3-quinolinecarboxylic acid, and 4,8 dihydroxyquinoline-2-carboxylic acid. Examples of cap monomers that can be used to cap a free NH 2 and form part of the nucleoside peptide molecules include but are not limited to methyl (Me), formyl (CHO), ethyl (Et), acetyl (Ac), t-butyl (t-bu), anisyl, trifluoroacetyl (Tfa), benzoyl (Bz), 4 15 methylbenzyl (Meb), thioanizyl, thiocresyl, benzyloxymethyl, 4-nitrophenyl (Pnp), benzyloxycarbonyl (Z), 2-nitrobenzoyl (NBz), 2-nitrophenylsulphenyl (Nps), 4-toluenesulphonyl (Tosyl, Tos), pentafluorophenyl (Pfp), diphenylmethyl (Dpm), 2-chlorobenzyloxycarbonyl (CI-Z), 2,4,5 trichlorophenyl, 2-bromobenzyloxycarbonyl (Br-Z), triphenylmethyl (Trityl, Trt), 2,2,5,7,8 pentamethyl-chroman-6-sulphonyl (Pmc), t-butyloxycarbonyl (Boc), benzyl (Bzl), benzyloxymethyl 20 (Bom), and 9-fluorenylmethyloxycarbony(Fmoc). Sugar transition state analogues (e.g. GlcNAc analogues) may be coupled to the nucleoside peptide molecules in a position in space close to where a sugar-phosphate bond would be cleaved in a corresponding sugar nucleotide donor. Specific examples of nucleoside peptide molecules of the invention have the formula I: 25 O x NH X 30 R wherein X is H, -COOH, -OSO 3 H, (CH 2 )qSO 3 H where q is 0 or 1, or -OPO 3 H, and R represents (Y)m where Y is a substituted amide group (e.g. an amide linked amino acid residue) and m is 1-3, Z' and Z 35 are the same or different and represent hydroxyl or alkoxy, or Z' and Z together form an acetonide group, and wherein free NH 2 groups in the compound of the formula I are preferably capped with the cap monomers mentioned herein, preferably with Fmoc or Boc.

WO 99/64378 PCT/CA99/00550 -9 Specific examples of nucleoside peptide molecules of the invention have the formula I wherein X is H, -COOH, -OSO 3 H, or (CH 2 )qSO 3 H where q is 0 or 1, Z and Z' are both hydroxyl or together form an acetonide group, R represents -NHCOR', wherein R' represents 5 (a) -C(CH 3

)NH

2

)CH

2 /Q) -R2, wherein R 2 is alkoxy; or (b) -CHR 3

R

4 wherein R 3 is hydrogen or -NH2 and R 4 is -R 5 wherein R 5 is 10 halogen, alkyl, or alkoxy, , -CH 2

N(CH

3

)CH

2

CH

2

R

6 or - N(CH 3

)CH

2

CH

2

R

6 wherein R 6 is halogen, 15 -CH 2

N(CH

3 )CO- j , -CH 2

N(C

2

H

5

)CH

2

CH(CH

3 )OH, or -CH 2

NHCOCH(CH

3

)

2 , or

R

4 represents (CH 2 ).Rg wherein n = 0 to 5, R8 is halogen, Q R9 wherein R 9 is 20 alkoxy, , "N

-N(CH

3

)CH

2

CH

2 R'* wherein R1 0 is halogen, -N(C 2

H

5

)CH

2

CH(CH

3 )OH, or -NHCOCH(CH 3

)

2 and wherein free amino groups are protected with a cap monomer. In an embodiment of a compound of the formula I of the invention, X is -COOH, and R 25 represents -NHCOR' wherein R1 represents -CHR 3

R

4 wherein R 3 is hydrogen, and R 4 is (CH 2 )nRl wherein n = 0 to 5, preferably 1 to 4, R 8 is halogen, R9 wherein R 9 is alkoxy, halogen, or alkyl, 30 , -- N , "N or -N(CH 3

)CH

2

CH

2 R'* wherein R1 0 is halogen, -N(C 2

H

5

)CH

2

CH(CH

3 )OH, or -NHCOCH(CH 3

)

2 . In another embodiment of the invention, a compound of the formula I is provided wherein , X 35 is -COOH, and R represents -NHCOR' wherein R' represents -CHR 3

R

4 wherein R 3 represents -NH 2 , and R 4 is -R 5 wherein R 5 is halogen, alkyl or alkoxy, -Hc -- .. a---. f5 IIC O WO 99/64378 PCT/CA99/00550 -10

-CH

2

N(CH

3

)CH

2

CH

2

R

6 wherein R 6 is halogen, -CH 2

N(C

2 Hs)CH 2

CH(CH

3 )OH,

CHNHCOCH(CH

3 )2 5 0 or -CH2N(CH 3 )CO-j In a further embodiment of the invention, a compound of the formula I is provided wherein X is -OSO 3 H, or (CH 2 )qSO 3 H where q is 0 or 1, R represents -NHCOR' wherein R' represents -CHR 3

R

4 10 wherein R 3 represents -NH 2 . and R 4 is R wherein R' is halogen, alkyl, or alkoxy, -CH 2 N(C2H 5

)CH

2

CH(CH

3 )OH, or

-CHNHCOCH(CH

3

)

2 . 15 In a particular embodiment, a nucleoside peptide molecule of the formula I is provided wherein X is -COOH, R is represents -NHCOR' wherein R1 represents -C (CH 3

)(NH-)CH

2 R2 wherein R 2 is alkoxy. 20 As used herein the term "alkyl", alone or in combination, refers to a branched or linear hydrocarbon radical, typically containing from I through 10 carbon atoms, preferably I through 5. Typical alkyl groups include but are not limited to methyl, ethyl, I -propyl, 2-propyl, 1 -butyl, 2-butyl, tert-butyl, or pentyl, preferably methyl or ethyl. The term "alkoxy" refers to an alkyl linked to the parent molecular moiety through an oxygen 25 atom. Examples of alkoxy groups include 0-methyl i.e. methoxy, 0-allyl i.e. allyloxy, 0-propyl i.e. propoxy, O-butyl i.e. butoxy, and the like, preferably methoxy or allyloxy. The term "halo" or "halogen", alone or in combination, refers to a member of the family fluorine, chlorine, bromine, or iodine. Specific examples of nucleoside peptide molecules are shown in Tables 3, 4, and 5. 30 In the nucleoside peptide molecules of the invention the stereochemistry of chiral carbon atoms in the nucleoside monomer unit, spacer monomer unit, or cap monomer unit can independently be in the R or S configuration, or a mixture of the two. For example, amino acids of the spacer monomer can be in the L-or D-configuration, resulting in the same amino acid, varying only in its stereochemistry. Therefore, the present invention encompasses a nucleoside peptide molecule of the 35 invention as a mixture of diastereomers, as well as in the form of an individual diastereomer, and the present invention encompasses a nucleoside peptide molecule as a mixture of enantiomers, as well as in the form of an individual enantiomer. All optical isomers and racemic forms thereof of the nucleoside peptide molecules of the invention are contemplated herein, and the nucleoside peptide molecules shown herein are intended to encompass all possible optical isomers of the compounds so depicted.

WO 99/64378 PCT/CA99/00550 The formation of diastereomers may be carried out pre or post spacer attachment to the nucleoside monomer unit by using L and/or D amino acids during synthesis or by racemizing chiral centers after spacer attachment or construction with base. Nucleoside peptide molecules of the invention may be present as pharmaceutically acceptable 5 salts. The term "pharmaceutically acceptable salts" encompasses those salts that form by standard acid base reactions with basic groups and organic or inorganic acids, or acidic groups and bases. Examples of acids include hydrochloric, sulfuric, phosphoric, acetic, succinic, citric, lactic, maleic, fumaric, palmitic, cholic, pamoic, mucic, D-glutamic, d-camphoric, glutaric, phthalic, tartaric, lauric, stearic, salicyclic, methanesulfonic, benezenesulfonic,sorbic, benzoic. cinnamic, and like acids. Examples of bases include 10 LiOH. NaOH, KOK and Ca(CH 2 ). Basic amino acids (e.g. glycine, ornithine, histidine, phenylglycine, lysine, and arginine) in a spacer monomer unit may be in protonated forms. Preparation of a Combinatorial Library A monomer unit is chemically conjugated i.e. covalently linked or coupled, to an adjoining monomer unit or building block to prepare a combinatorial library of the invention. After conjugation, 15 a monomer unit is altered, for example, upon reaction to form a covalent bond, the monomer can lose a water molecule, or can undergo formation of a urea or carbamate group. There are innumerable variations in the nature of the monomer units and in the types of chemical reactions that can be used to chemically conjugate the monomers. In addition, solid phase and solution phase chemistries may be used to synthesize a combinatorial library of the invention. 20 The building blocks or monomers used in the compounds contained in the library of the invention may be assembled "backwards" i.e. the last building block added to the "growing chain" may be analogous to the 5' terminal end of a peptide or polypeptide. For example, in a library schematically depicted as uridine-spacer-cap, the uridine building block or monomeric unit may be chemically conjugated to an adjoining spacer unit last in time. In this scheme, the cap monomeric unit is generally 25 attached to a solid phase matrix until release of uridine-spacer-cap following the last chemical conjugation reaction. Examples of processes for preparing compounds in combinatorial libraries of the invention are set out below. A combinatorial library of the invention where the reactive group on the nucleoside monomer 30 unit is an amine may be prepared using an acetonide, or other suitable protecting groups to temporarily protect chemically active sites. In particular, a library based on uridine structures may be produced. using a 5'-deoxy-5'-amino-2',3'-O-isopropylidinyluidine template. The template may be prepared by acetonide blockage of the 2'- and 3'-hydroxyl groups, activation of the 5'hydroxy using mesylation, tosylation, or triflation, subsequent reaction with sodium azide, and reduction (for example, see Figures 35 1 to 4). A spacer monomer unit comprising an amino acid, dipeptide, or tripeptide which is suitably protected, e.g. N-t-butyloxycarbonyl (Boc), or N-9-fluorenylmethyloxycarbonyl(Fmoc)-protected, may be coupled with the uridine template in free base form ((for example, see Figure 5). This is followed by deprotection (see for example, Figure 6). Purification of the nucleoside peptide monomer unit and spacer unit is carried out using conventional methods, and the free amine bases may be capped with for WO 99/64378 PCT/CA99/00550 - 12 example, carboxylic acids, anhydrides, esters, isocyanates. isothiocyanate, acid chloride, or aldehydes (see for example, Figure 7). The invention also contemplates intermediates used in the processes of the invention, including nucleoside peptide molecules of the combinatorial libraries of the invention having a 5 protected hydroxy in the heterocyclic amine base and/or which may be blocked at the 2' or 3' hydroxyls. The spacer monomer unit may be coupled to the nucleoside monomer unit using a synthetic strategy that consists of three chemical steps and two purification steps, all of which can be automated. Examples of reaction schemes for adding the spacer monomer unit are shown in Figures 5 and 6. The 10 reactions may be performed in deep well (1 or 2 mL), 96-well-formatmicrotitre plates. The first step is to couple Boc- protected amino acids, dipeptides or tripeptides to the uridine template in free base form. This is followed by concomitant N-deprotection and acetonide deblockage using an excess of TFA. The TFA salts are neutralized by ion exchange slurrying using a PolyfiltronicsTM unifilter plate (in 96 well format), allowing for the generation of free amine residues. The free amine groups are capped for example 15 with isocyanates, isothiocyanates. carboxylic acids, sulfonyl chlorides, and acyl chlorides to give five libraries of products. Purification, if necessary, can be carried out by slurrying with aminomethyl resin, which scavenges any excess capping reagent, or with alumina silica or FlorisilTM which retains excess reagents and byproducts. The slurrying can be performed in a PolyfiltronicsTM plate. The free terminal amine groups may also be capped with aldehydes under reductive amination conditions. For benzyl ester 20 protected derivatives (e.g. aspartic acid and glutamic acid residues in the spacer monomer unit), manual transfer hydrogenation using ammonium formate, Pd-C (10%, wet) and methanol, hydrolysis (TFA, H 2 O) or saponification (methanol, KOH, H 2 O) can be performed to liberate the carboxylate and racemize chiral amino acid fragments if desired. An alternative reaction scheme for adding spacer monomer units using an Fmoc strategy is 25 shown in Figure 7. The reactions may be performed in deep well (I or 2mL), 96-well format microtitre plates if desired. The first step is to couple Fmoc-protected amino acids, dipeptides or tripeptides to the free amine group of the uridine monomer template. This is followed by Fmoc deprotection with morpholine in DMF as solvent. This method liberates the free terminal amine without removing the isopropylidene protecting group. No neutralization step is necessary and morpholine is easily removed 30 by evaporation under reduced pressure. The terminal amines are then capped as required, as described above. The acetonide protecting group can be removed from all or selected capped or uncapped uridine peptides in a final reaction sequence by treatment with TFA at room temperature followed by evaporation of reagents and solvent under reduced pressure (see Figure 8). A combinatorial library of the invention where an amide group links a nucleoside monomer 35 unit and a spacer monomer unit may be prepared by forming a compound of the formula I where R represents -NHCOCHR 3

R

4 wherein R 3 is NH 2 using the method as described in N. P. Damodaran et al. J. Am. Chem.Soc. 93, 3812, 1971. The free amino form of the compound is subjected to condensation with a corresponding ester of R3 in aqueous DMF in the presence of N-methyl morpholine at an appropriate temperature. Other reactive esters such as N-hydroxy succinimidyl, hydroxybenzotriazole, WO 99/64378 PCT/CA99/00550 - 13 or pentafluorophenyl esters, or other reactive esters commonly used in peptide synthesis may also be used. For example, synthesis of a compound of the formula I where R 4 is (CH 2 )nR' where n is 2 and R, is halogen (compound A in Table 3) can be achieved by using the methyl ester of 1-fluorobutyric acid. Similarly, compounds B, C, and D in Table 3 can be synthesized by using an ester of the corresponding 5 acid, which can be synthesized by conventional methods. Compounds E to J in Table 3 can be synthesized by using the appropriate esters of the corresponding acids, which are commercially available. For compounds F to, H in Table 3, prior to condensation, the free amino group in the esterified reagent is blocked with a suitable group. A combinatorial library containing the selected compounds shown in Tables 4 and 5 where X 10 is sulphate can be synthesized by a similar condensation of an ester with a free amine. Predetermined compounds in the combinatorial library where C-5 of a uridine has different alkyl and aryl groups may be prepared by mercuration of commercially available UDP with mercuric acetate to give UDP-C-5-mercuric acetate, which on treatment with an appropriate alkene compound in the presence of potassium tetrachloropalladate produces the corresponding C-5-alkene derivative. On 15 selective reduction, these compounds give C-5-alkyl compounds. This type of derivatization is known as the Heck reaction and it can be carried out in a variety of ways known in the art (Ryabov, Synthesis (1985) 233-252; and Heck, Org. React. (1982) 27: 345-390). A transition state analogue of a sugar which is transferred by a sugar nucleotide donor may be coupled to a nucleoside peptide molecule of the invention. For example, a GlcNAc cation analogue can 20 be generated, and prepared in a form that would allow it to be coupled to a uridine ribose molecule of the invention. Bioassays The combinatorial library of the invention contains putative inhibitors of carbohydrate processing enzymes. Inhibitors with appropriate selectivity and activity against a particular 25 carbohydrate processing enzyme may be selected using conventional bioassays and the bioassays described herein. Bioassays may be adapted for high throughput screening incorporating automation and robotics to enable testing thousands to millions of compounds in a relatively short time. Preliminary screening of 5408 compounds from a library of the invention, revealed that 2-3% of the compounds had inhibitory activity in conventional core 2 GIcNAc-T, GIcNAc-TV, and GlcNAc-TI 30 assays. Once "lead" compounds are identified using the screening techniques, combinatorial chemistry methods can be used to optimize the initial leads. The optimized analogs/variants can be tested in the same screening assays that identified the initial lead. The methods designed by the present inventors described herein use simple, and rapid 35 functional assays that can identify one or more active ingredients in tested pools without the need for a long deconvolution process. The assays are used in robotics systems that can handle large numbers of samples for proportioning, mixing, and sample-handling. The invention therefore makes available robotics that can perform multiple chemical reactions at variable temperatures, and subsequently handle work up and characterization of bioactive leads. The selection means enable identification of WO 99/64378 PCT/CA99/00550 - 14 active compounds within the combinatorial libraries that can generate affinity enrichment or affinity selection, and this enrichment and selection may be followed by mass spectroscopic identification of any bioactive compounds. The present invention contemplates a solid-phase bioassay for identifying a compound in a 5 combinatorial library of the invention having inhibitory activity against a carbohydrate processing enzyme including glycosyitransferases or glycosidases. The method is particularly useful for drug screening. The solid-phase bioassay involves coupling a carbohydrate acceptor for the carbohydrate processing enzyme to a polymer and coating onto a carrier or support. A carbohydrate processing enzyme, a sugar nucleotide donor labeled with a detectable substance, and a test compound are added, 10 and the detectable change produced by the detectable substance is measured. Examples of polymers to which an acceptor may be coupled include polyacrylamide. The carrier or support may be for example nitrocellulose, or glass, gabbros. or magnetite. The support material may have any possible configuration including spherical (e.g. bead), cylindrical (e.g. inside surface of a test tube or well, or the external surface of a rod), or flat (e.g. sheet, test strip). 15 Examples of detectable substances include, but are not limited to, radioisotopes (e.g., 3 H, 1 4 C, 35 S, 1251, 311), fluorescent labels (e.g., FITC, rhodamine, lanthanide phosphors), luminescent labels such as luminol. enzymatic labels (e.g., horseradish peroxidase, beta.-galactosidase, luciferase. alkaline phosphatase. acetylcholinesterase), and biotinyl groups (which can be detected by marked avidin e.g., streptavidin containing a fluorescent marker or enzymatic activity that can be detected by optical or 20 calorimetric methods). In an embodiment of the invention, the detectable substance is a radioactive material, most preferably tritium. A carbohydrate processing enzyme used in the method may be obtained using conventional extraction methods from natural sources, it may be a recombinant enzyme, or it may be obtained from commercial sources. 25 In an embodiment of the invention, the assay involves coupling carbohydrate acceptors to a polymer (e.g. polyacrylamide) and coating onto a carrier, such as the surface of 96 well plastic plates. The glycosyltransferase reaction is performed with recombinant enzymes and a tritiated sugar nucleotide donor, followed by washing, addition of scintillation counting fluid, and measurement of radioactivity with a B-counter. Glycopolymer construction and coating of the plastic plates, enzyme and 30 substrate concentrations, and linearity with time were optimized using UDP-GicNAc:GalB1-3GaINAc R BI-6-N-acetylglucosaminyltransferase (GIcNAc to GaINAc) (i.e. core 2 GIcNAc-T), a rate-limiting reaction for expression of polylactosamine and the selectin ligand sialy Lewisx. Polylactosamine expression has been associated with malignant transformation (Itzkowitz, SH et al., Cancer Res., 46, 2627-2632, 1986; Kim YS et al., Cancer Res. 46, 5985-5992, 1986,), development (Pennington JE et 35 al., JEmbrvol., 90, 335-361, 1985) and proliferative activation of lymphocytes (Higgins EA et al., J.Biol.Chem.. 266. 6280-6290, 1991). Polylactosamine structures have been shown to play a significant role in cell-cell and cell-substratum adhesion processes (Zhu BC and Laine RA. JBiol. Chem., 260, 4041-4045. 1985: Laferte' S and Dennis JW. Cancer Res., 48, 4743-4748, 1988). Additionally, they WO 99/64378 PCT/CA99/00550 - 15 may act as ligands for mammalian lectins (Merkle RK and Cummings RD, J.Biol.Chem., 263, 16143 16149, 1988). In a screen to detect core 2 GlcNAc-T inhibitors in a microbial extract library, the CV for positive controls was +/- 9.4 %, and complete concordance for hit validation was observed between the 5 solid phase assay and a standard solution assay. A glycosyltransferase assay can be used to identify inhibitors of a variety of carbohydrate processing enzymes, including the enzymes described herein, preferably core 2 GlcNAc-T, GlcNAc-TI and GIcNAc-TV. Lectin-sensitivity assays have been largely employed to study the carbohydrate patterns of cell 10 lines. By specifically binding to oligosaccharide structures at the cell surface, lectins generally exert a cytotoxic effect causing growth disadvantage. L-PHA is a lectin which recognizes tri- and tetra antennary N-linked oligosaccharides carrying the structure (GalPl,4GIcNAcP3I,6)Galp l,4 GlcNAcP1.2Mano:), thus representing a valid probe for detection of P 1,6 branched, complex-type oligosaccharides. These structures are associated with tumor progression and appear on malignant cells 15 (Dennis et al., 1986) [for example the murine lymphoreticular, highly metastatic, tumor model MDAY D2 line (VanderElst and Dennis. 1991)]. Reduction and/or truncation of cell surface N-linked carbohydrate chains in MDAY-D2 cells is directly correlated with decreasing levels of L-PHA sensitivity and, in turn, with improving cell proliferation even in the presence of the lectin. Thus, such a system can be exploited for revealing any means blocking the biosynthesis of 1,6, branched N-linked 20 structures. Given the functional significance of complex N-oligosaccharides during malignant transformation, large-scale L-PHA assays have been developed by the present inventors to identify compounds in the combinatorial libraries that are new inhibitors of the N-linked oligosaccharide processing pathway. The terms "N-linked oligosaccharide processing" or "N-linked oligosaccharide processing 25 pathway" refer to the biosynthetic pathway for the in vivo synthesis of glycoproteins with N-linked oligosaccharides. N-linked oligosaccharides are linked to the amide N in the sidechain of Asn in the consensus sequence Asn-X-Ser/Thr of the protein moiety, where X can be any amino acid. The method of the invention can be particularly applied to identify compounds that inhibit complex-type N-linked oligosaccharides, in particular p 1,6- branched complex-type oligosaccharides associated with tumor 30 growth and metastasis. N-linked oligosaccharide processing involves the synthesis of a precursor molecule, transfer of the precursor to Asn by oligosaccharyltransferase followed by further processing by membrane-bound glucosidases and endoplasmic reticulum a 1,2-mannosidase, and transport from the rough endoplasmic reticulum to the Golgi stacks. In the Golgi stacks, further processing occurs depending on the final destination of the glycoprotein and it may involve lysosomal enzymes or 35 nonlysosomal enzymes. Complex and hybrid type oligosaccharide chains are synthesized through the second nonlysosomal processing pathway and residues can be added by enzymes including Golgi mannosidase I (a 1.2 specific), and N-acetylglucosaminyltransferases I, II, and III (A description of the N-linked processing pathway may be found at http://www.uni.mainz.de/-frosc000/STRU22.html).

WO 99/64378 PCT/CA99/00550 -16 The L-PHA method of the invention can be used to identify compounds that inhibit all steps in the N-linked oligosaccharide pathway prior to P1,4 Gal transferase, including compounds that inhibit the carbohydrate processing enzymes described herein, and Golgi a-mannosidases. In an embodiment of the invention, a fully automated enzymatic method is contemplated that 5 is based on measurement of alkaline phosphatase activity. The method is based on the observation that the number of cells and their level of alkaline phosphatase activity are closely correlated. The method employs a colorimetric assay to monitor cell proliferation of transformed cells after L-PHA treatment. The reaction mixture is directly added to cells growing in their own medium. Thus, the method can be carried out in a single step, without removal of the culture medium or cell pelletting and washing, 10 thereby permitting the fully automated procedures. The assay method is also highly reproducible (CV=4%) and inexpensive, thus representing a valuable tool when large-scale experiments are performed. The reaction is linear with time in a wide time interval (5-180 min), and the Km value of the enzyme for the substrate para-nitrophenylphosphate is relatively low (0.81 mM). Incubation time and substrate concentration can be changed in order to modulate the velocity of the reaction and adjust 15 the protocol, for automation and timing purposes, to the number of samples. Use of a robotic platform also allows simultaneous processing of large numbers of samples, e.g. thirty-six 96-well plates. Therefore. an automated method is provided for testing a compound for its ability to inhibit N linked oligosaccharide processing comprising (a) incubating the compound with cells expressing N linked oligosaccharides (preferably P 1,6 branched, complex-type oligosaccharides) in the presence of 20 L-PHA, and measuring alkaline phosphatase activity; and (b) comparing to a control in the absence of the compound wherein higher alkaline phosphatase activity indicates that the compound has the ability to inhibit N-linked oligosaccharide processing. The method may be used to identify compounds which inhibit all steps in the N-linked oligosaccharide pathway prior to P1,-4 Gal-transferases, including compounds that inhibit the carbohydrate processing enzymes described herein, in particular N 25 acetylglycosaminyltransferases, including N-acetylglucosaminyltransferases I, II and V. The method may also be used to identify compounds that inhibit Golgi c-mannosidases. The automated method of the invention can generally be used to identify antagonists of cell growth inhibitors, such as TGF-P, IL-ly , TNFa, and IFN. Therefore, the invention broadly contemplates a method comprising (a) reacting a test compound with cells expressing N-linked 30 oligosaccharides in the presence of a cell growth inhibitor; (b) measuring alkaline phosphatase activity ; and (c) comparing to a control in the absence of the test compound wherein an increase in alkaline phosphatase activity indicates that the compound has the ability to antagonize the cell growth inhibitor. Cells which can be used in the methods of the invention include MDAY-D2, L1210, melanoma tumor cells, and human tumor cells such as SW 480, LS I 74T, HT-29, WiDr, T2, MDA-23 1, 35 MCF7, BT-20, Hs578T, K562, Hs578T, SK-BR-3, CY 6T, MDA-468, H23, H157, H358, H1334, H 1155, H28, H460, Hmesol, H 187, H5 1 OA, N417, H 146, H 1092, H82 (Restifo. N. P. et al, J. Exper. Med. 177:265-272, 1993). The cell lines may contain either constitutive or inducible enzyme activity such as osteoblastic cell lines.

WO 99/64378 PCT/CA99/00550 -17 Cell proliferation is measured by measuring alkaline phosphatase activity. Alkaline phosphatase may be measured using conventional methods for example by using para nitrophenylphosphate as a substrate and measuring absorbance at about 405nm. The conditions for carrying out the method will be selected having regard to the nature of the 5 compound and the cells employed. For example, if the cells are MDAY-D2 tumor cells a concentration of about 1-6 x 10 3 cells, preferably 5 x 10 3 may be used. The MDAY-D2 cells are generally cultured for about 10 to 30 hours, preferably 16 to 20 hours, followed by addition of L-PHA at a concentration of about 50 to 150 pg/mL, preferably 100 pg/mL. The alkaline phosphatase assay mixture may contain a buffer e.g. diethanolamine buffer, and para-nitrophenylphosphate at an initial concentration of about 10 1.5 to 4 mM, preferably 2 to 3 mM, most preferably 2.5 mM. Utility of Inhibitors Small molecule inhibitors with appropriate selectivity and activity against a particular carbohydrate processing enzyme can be selected from the combinatorial libraries of the invention using high throughput screening bioassays. The selected small molecule inhibitors will have valuable 15 pharmacological properties. In particular, the inhibitors will be useful in the treatment and prophylaxis of tumor growth and metastasis of tumors. Anti-metastatic effects of inhibitors can be demonstrated using a lung colonization assay. For example, melanoma cells treated with an inhibitor may be injected into mice and the ability of the melanoma cells to colonize the lungs of the mice may be examined by counting tumor nodules on the lungs after death. Suppression of tumor growth in mice by the inhibitor 20 administered orally or intravenously may be examined by measuring tumor volume. A small molecule inhibitor can have particular application in the prevention of tumor recurrence after surgery i.e. as an adjuvant therapy. A small molecule inhibitor can be especially useful in the treatment of various forms of neoplasia such as leukemias, lymphomas. melanomas, adenomas. sarcomas, and carcinomas of solid 25 tissues in patients. In particular, the small molecule inhibitors can be used for treating malignant melanoma, pancreatic cancer, cervico-uterine cancer, ovarian cancer, cancer of the kidney such as metastatic renal cell carcinoma, stomach, lung, rectum, breast, bowel, gastric, liver, thyroid, head and neck cancers such as unresectable head and neck cancers, lymphangitis carcinamatosis, cancers of the cervix, breast, salivary gland, leg, tongue, lip, bile duct, pelvis, mediastinum, urethra, bronchogenic, 30 bladder, esophagus and colon, non-small cell lung cancer, and Kaposi's Sarcoma which is a form of cancer associated with HIV-infected patients with Acquired Immune Deficiency Syndrome (AIDS). The inhibitors may also be used for other anti-proliferative conditions such as bacterial and viral infections, in particular AIDS. A small molecule inhibitor of the present invention can be used to treat immunocompromised 35 subjects. For example, they can be used in a subject infected with HIV, or other viruses or infectious agents including bacteria, fungi, and parasites, in a subject undergoing bone marrow transplants, and in subjects with chemical or tumor-induced immune suppression. A small molecule inhibitor can be used as hemorestorative agents and in particular to stimulate bone marrow cell proliferation, in particular following chemotherapy or radiotherapy. The WO 99/64378 PCT/CA99/00550 - 18 myeloproliferative activity of an inhibitor of the invention may be determined by injecting the inhibitor into mice. sacrificing the mice, removing bone marrow cells and measuring the ability of the inhibitor to stimulate bone marrow proliferation by directly counting bone marrow cells and by measuring clonogenic progenitor cells in methylcellulose assays. The inhibitors can also be used as 5 chemoprotectants and in particular to protect mucosal epithelium following chemotherapy. A small molecule inhibitor of the invention also can be used as an antiviral agent in particular on membrane enveloped virusessuch as retroviruses, influenza viruses, cytomegaloviruses and herpes viruses. A small molecule inhibitor can also be used to treat bacterial. fungal, and parasitic infections. For example, a small molecule inhibitor can be used to prevent or treat infections caused by the 10 following: Neisseria species such as Neisseria meningitidis. and N. gonorrheae; Chlamydia species such as Chlamydia pneumoniae Chlamydia psittaci, Chlamvdia trichomatis; Escherichia coli. Haemophilus species such as Haemophilus influenza; Yersinia enterocolitica: Salmonella species such as S.tvphimurium; Shigella species such as Shigella flexneri; Streptococcus species such as S.agalactiae and S. pneumoniae; Bacill/us species such as Bacillus subtilis: Branhamella catarrhalis; 15 Borrelia burgdorfer; Pseudomonas aeruginosa; Coxiella burnetti; Campylobacter species such as C.hyoilei; Helicobacter pylori; and, Klebsiella species such as Klebsiella pneumoniae. A small molecule inhibitor can also be used in the treatment of inflammatory diseases such as rheumatoid arthritis, asthma, inflammatory bowel disease, and atherosclerosis. A small molecule inhibitor can also be used to augment the anti-cancer effects of agents such 20 as interleukin-2 and poly-IC, to augment natural killer and macrophage tumoricidal activity, induce cytokine synthesis and secretion, enhance expression of LAK and HLA class I specific antigens; activate protein kinase C. stimulate bone marrow cell proliferation including hematopoietic progenitor cell proliferation, and increase engraftment efficiency and colony-forming unit activity, to confer protection against chemotherapy and radiation therapy (e.g. chemoprotective and radioprotective 25 agents), and to accelerate recovery of bone marrow cellularity particularly when used in combination with chemical agents commonly used in the treatment of human diseases including cancer and acquired immune deficiency syndrome (AIDS). For example, a small molecule inhibitor can be used as a chemoprotectant in combination with anti-cancer agents including doxorubicin, 5-fluorouracil, cyclophosphamide, and methotrexate, and in combination with isoniazid or NSAID. 30 The term "patient" herein refers to a warm-blooded animal such as a mammal which is afflicted with a particular disease state or condition as described herein. Examples of animals within the scope of the meaning of the term are dogs, cats, rats, mice, horses, bovine cattle, sheep, and humans. Small molecule inhibitors can be converted using customary methods into pharmaceutical 35 compositions. The pharmaceutical compositions contain the inhibitors either alone or together with other active substances. Such pharmaceutical compositions can be for oral, topical, rectal, parenteral, local, inhalant, or intracerebral use. They are therefore in solid or semisolid form, for example pills, tablets. creams, gelatin capsules, capsules, suppositories, soft gelatin capsules, liposomes (see for example, U.S. Patent No. 5,376,452), gels, membranes, and tubelets. For parenteral and intracerebral WO 99/64378 PCT/CA99/00550 -19 uses, those forms for intramuscular or subcutaneous administration can be used, or forms for infusion or intravenous or intracerebral injection can be used, and can therefore be prepared as solutions of the inhibitors or as powders of the inhibitors to be mixed with one or more pharmaceutically acceptable excipients or diluents, suitable for the aforesaid uses and with an osmolarity which is compatible with 5 the physiological fluids. For local use, those preparations in the form of creams or ointments for topical use or in the form of sprays should be considered; for inhalant uses, preparations in the form of sprays should be considered. The pharmaceutical compositions can be prepared by per se known methods for the preparation of pharmaceutically acceptable compositions which can be administered to patients, and 10 such that an effective quantity of the active substance is combined in a mixture with a pharmaceutically acceptable vehicle. Suitable vehicles are described, for example, in Remington's Pharmaceutical Sciences (Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., USA 1985). On this basis, the pharmaceutical compositions include, albeit not exclusively, the inhibitors in association with one or more pharmaceutically acceptable vehicles or diluents, and contained in 15 buffered solutions with a suitable pH and iso-osmotic with the physiological fluids. An inhibitor can be indicated as a therapeutic agent either alone or in conjunction with other therapeutic agents or other forms of treatment (e.g. chemotherapy or radiotherapy). An inhibitor can be used to enhance activation of macrophages, T cells, and NK cells in the treatment of cancer and immunosuppressive diseases. By way of example, an inhibitor can be used in combination with anti 20 proliferative agents, antimicrobial agents, immunostimulatory agents, or anti-inflammatories. In particular, an inhibitor can be used in combination with anti-viral and/or anti-proliferative agents, such as Thl cytokines including interleukin-2, interleukin-12, and interferon-y, and nucleoside analogues such as AZT and 3TC. The compounds of the invention may be administered concurrently, separately, or sequentially with other therapeutic agents or therapies. 25 Compositions containing small molecule inhibitors can be administered for prophylactic and/or therapeutic treatments. In therapeutic applications, compositions are administered to a patient already suffering from a disease or condition as described above, in an amount sufficient to cure or at least alleviate the symptoms of the disease and its complications. An amount adequate to accomplish this is defined as a "therapeutically effective dose". Amounts effective for this use will depend on the 30 severity of the disease, the weight and general state of the patient, the nature of the administration route, the nature of the formulation, and the time or interval at which it is administered. In prophylactic applications. compositions containing small molecule inhibitors are administered to a patient susceptible to or otherwise at risk of a particular disease. Such an amount is defined to be a "prophylactically effective dose". In this use, the precise amounts depend on the 35 patient's state of health and weight, the nature of the administration route, the nature of the formulation, and the time or interval at which it is administered. It will be appreciated that where major amounts are administered for a therapeutic or prophylactic treatment, it may be advisable to divide these into several administrations over the course of a day.

WO 99/64378 PCT/CA99/00550 - 20 The following examples illustrate the invention. EXAMPLE 1 CombinatorialSynthesis of GnT-V Inhibitors Below, the synthesis of 5'-deoxy-5'-amino-2',3'-O-isopropylidinyluridine and peptide 5 branched derivatives of 5'-deoxy-5'-amino-2',3'-O-isopropylidinyliridine are described. The invention contemplates intermediates, 2,3-0-isopropylidene-5-0-methanesulfonyl uridine, and 5-deoxy-5-azido 2,3-0-isopropylidenyluridine derivatives. I. Synthesis of 5'-deoxv-5'-amino-2',3'-O-isopropylidenyluridine A. Preparation of 2,3-0-isopropylidenyluridine (Figure 1) 10 Uridine (65.0 g, 266.2 mmoles), camphor sulfonic acid (1.0 g, 4.3 mmoles), 2,2-dimethoxy propane (98.0 mL, 798.5 mmoles), and acetone (anhydrous, 1000 mL) were stirred vigorously for 24 h at room temperature. The reaction was monitored by TLC (solvent system 7:93, MeOH:CHCI 3 ). Once the starting material was consumed, triethylamine (1.12 mL, 8.6 mmol) was added and the mixture stirred for another one hour. The acetone was evaporated under reduced pressure (<40 *C) to give a 15 white powder (77.0 g), which was used for the next step without any purification. B. Preparation of 2.3-O-Isopropylidene-5-O-methane sulfonvi uridine (Figure 2) The crude 2.3-0-isopropylidenyl uridine (77.0g; obtained in step A) was dissolved in DMF. Triethylamine (74.2 mL) was added and the mixture was cooled to 0 0 C. Methanesulfonyl chloride (31.2 mL) was then added dropwise during a 30-60 min. period while rapid stirring continued. After an 20 additional 1 hr of stirring at room temperature, the DMF was evaporated. The residue was dissolved in ethyl acetate (2.0 L) and washed three times with water (3 X 250 mL). The organic layer was dried over MgSO 4 , filtered, the filter cake rinsed with some EtOAc and the solvent evaporated. The light yellow residue (thick syrup) was used directly for the next step without further purification. The reaction was monitored by TLC (7:3, ethyl acetate : hexane). 25 C. Preparation of 5- azido-5-deoxv -2,3-0-isopropylidenyl uridine (Figure 3) The crude mesylate (obtained from step B above) was dissolved in DMF (400 mL, reagent grade) and stirred at 60*C with sodium azide (34.6g, 532 mmol) for 12 hrs until complete consumption of the mesylate was observed by TLC (TLC 7:3, ethyl acetate: hexane). The mixture was filtered through a Celite bed. The filtrate was evaporated to dryness. The residue was dissolved in ethyl acetate 30 (2.0 L) and washed three times with water (3 X 250 mL). The organic layer was dried over MgSO 4 and evaporated under reduced pressure at 30*C. The solid residue was recrystallized from ethyl acetate/hexane (1:1) to afford 65.0g of the desired azido uridine as a white crystalline solid (mp 11 8*C ). 'H NMR (500 MHz, CD 3 0D): 1.34, 1.53 (2s, 6H); 3.52 (dd, IH, J = 4.4, 12.9 Hz); 3.6 (dd, IH, J 5.9, 12.9 Hz); 4.2 (ddd, I H, J = 4.4, 4.4, 6.2 Hz); 4.8 (dd, 1H, J= 4.2, 6.2 Hz); 5.06 (dd, 1H, 2.3, 6.2 35 Hz); 5.7 (d, IH, J = 7.8 Hz); 5.78 (d, I H, J = 2.2 Hz); 7.65 (d, I H, J = 8.0 Hz). D. Preparation of 5-amino-5-deoxv -2,3-0-isopropylidenyl uridine (Figure 4) 5.Og of azide was dissolved in ethanol (150-200mL). To this solution, Pd(OH)2 and NaHCO 3 was added. The reaction flask was evacuated and filled with H 2 gas. This was repeated three times and the mixture was stirred for 3-6h at room temperature under H 2 . The mixture was filtered through a WO 99/64378 PCT/CA99/00550 -21 Celite bed and evaporated. The residue was used for capping and peptide coupling reactions. 'H NMR (500 MHz, CDCl 3 ): 1.35, 1.57 (2s, 6H); 2.95 (dd, l H, J = 6.0, 13.6 Hz); 3.06 (dd, I H, J = 4.6, 13.6 Hz); 4.1 (appear as dd, in fact it is ddd, 1 H, J = 4.3, 4.35, 6.4 Hz); 4.76 (dd, I H, J= 4.5, 6.4 Hz); 4.95 (dd, IH, 2.6, 6.4 Hz); 5.7 (d, lH, J = 2.4 Hz); 5.73(d, IH, J = 8.1 Hz); 7.38(d, lH. J = 8.2 Hz). 5 II. Coupling Procedure (Fi2ure 5) Free amine (Figure 5) was dissolved in dichloromethane (250 mL) and WSC.HCI [l-ethyl-3 (3'-dimethylaminopropyl)carbodiimide .HCI, 1.2 eq] was added. To this clear solution, N-t butoxycarbonyl protected amino acids (1.0 eq) were added and stirred under argon for 1-3 h. The reaction was monitored by TLC (7: 93, MeOH/CHC 3 ). After the reaction was complete, more 10 dichloromethane was added and the solution washed with water (for a few amino acids like glutamine, o-nitroarginine, asparagine water wash is not possible, because the derivatives are water soluble), and the organic layer was dried over MgSO 4 and evaporated . The residue was purified by column chromatography (eluent 2-5% MeOH in CH 2 Cl 2 ) to give white solids. Yields vary from 75-85%). This procedure was performed on 25.0g scales. In a similar fashion, free amine (1 eq), N-FMOC-protected 15 amino acids (1.leq) and HBTU in DMF (1.1 eq) were reacted to give N-FMOC protected uridine monopeptides. III. N-Boc Deprotection (Figure 6) Uridine peptides (Figure 6) were treated separately with TFA/CHCl 3

/H

2 0 (3:4:1) at room temperature for 12 hours. Excess reagent and solvent were evaporated under reduced pressure. The 20 residue was dissolved in methanol, treated with OH~ resin until neutral, filtered, and evaporated to dryness. IV. Capping (Figure 8) Fully deprotected uridine monopeptide and dipeptide derivatives were treated separately with capping reagents (acyl chloride, isocyanate, and thioisocyanate, 1.2 eq) and diisopropylethyl amine (1.5 25 eq) in DMF at room temperature. After 12h, solvent was removed and the residues were dissolved in methanol. These solutions were treated with aminomethylated polystyrene resin for 48 hours to quench excess capping reagent. Mixtures were filtered, evaporated, and dissolved in DMSO. N-t-Boc and N-FMOC-deprotected dipeptides (I eq) were also capped with various carboxylic acid caps (1.05-1.2 eq) in the presence of HBTU (1.05-1.2 eq) in DMF. The solvent was evaporated 30 under reduced pressure (temp 600). The residues were dissolved in 8/8/1 [MeCN/MeOH/H 2 O], and then filtered individually through a pad of basic alumina in a 96-well format using polytronics filter plates. The solvents were again evaporated under reduced pressure ( 400), and the residues diluted in DMSO for storage and testing. Fully deprotected monopeptide and dipeptide derivatives were also successfully capped 35 separately with a variety of carboxylic acids (1.1 equiv.) with ethyl diisopropylamine in DMF via a carbodiimide coupling with or without HOBT or by an HBTU assisted protocol. EXAMPLE 2 ABBREVIATIONS Gal D-galactose WO 99/64378 PCT/CA99/00550 -22 GaINAc D-N-acetylgalactosamine GIcNAc D-N-acetylglucosamine FCS fetal calf serum T transferase 5 A solid-phase glycosyltransferase assay was developed for drug screening. Glycosyltransferases catalyze the formation of glycosydic linkages between monosaccharides donated by sugar-nucleotide. and specific .oligosaccharide acceptors. The solid-phase assay was illustrated for core 2 GlcNAc-T and can be adapted for other glycosyltransferases. The assay utilizes multivalent oligosaccharide acceptors linked to polymer coated plastic plates and thereby eliminates the need for 10 chromatographic separation of product. MATERIALS AND METHODS Chemicals: Poly[N-(acryloyloxy)succinimide] (pNAS) (1, Figure 9) with a viscosity-average molecular weight M, of 42.1 kDa (DP ~250) was prepared according to Mammen et al. (Mammen et al J. Med. Chem., 38, 4179-41901995). Disaccharide Galpl-3GaNAca-O(CH) 3

S(CH)

2

NH

2 (2) (core 2 15 GIcNAc-T acceptor) and [GlcNAc(il-2)]Man( 1-6)Glc( -O(CH 2

)

3

S(CH,)NH

2 ) were prepared from the corresponding allyl glycoside following a procedure described by Roy and Tropper (R. Roy and F.D. Tropper, J. Chem. Soc. Chem. Commun. 1058 (1988): Glycoconjugate J. 5:203 (1988)). GalIl 3GalNAca-pNp and GalNAca-polymers UDP-6-[3H]-N-acetylglucosamine (16.0 Ci/mmol) were purchased from Toronto Research Chemicals (Toronto, Canada) while non labelled UDP-6-N 20 acetylglucosamine was obtained from Sigma Chemicals. Glycopolymer syntheses: Poly[N-(acryloyloxy)succinimide] (1) was first treated at room temperature with the amine-terminated T-antigen disaccharide 2 in DMSO (16 h) to provide a core copolymer containing one sugar residue for every ten N-substituted acrylamide residues. The active ester containing polymer was then treated at room temperature for three hours with excess primary amines 25 (ammonia. methylamine, ethylamine, or propylamine) to give four different copolymers 3-6 having the same comonomer ratios but differing by the lipophilicity of the copolymer backbones. The glycopolymers were then purified by size exclusion chromatography over BioGel P-10 using water as eluent. Alternatively, disaccharide 2 was treated with methacryloyl chloride and the resulting monomer was copolymerized with methacrylamide to provide copolymer 8, while direct 30 copolymerization of allyl glycoside precursor of 2 with acrylamide gave copolymer 10. Using the same strategy, copolymer acceptors 11-14 for GlcNAc-T V were prepared using the same core pNAS 1 and molar ratios of acrylamide:sugar of 10:1 (Figure 10). Recombinant core 2 GIcNAc-T: A truncated form of core 2 GIcNAc-T cDNA, lacking 37 amino acids from the N-terminus was prepared by PCR. The truncated cDNA was cloned in-frame into 35 pPROTA vector (Sanchez-Lopez et al., J. Biol. Chem. 263, 11892-118991988) for expression as a secreted protein A chimeric protein. The expression vector was co-transfected into CHO cells, along with pSV2neo, in a 10:1 molar ratio, using a calcium phosphate method. Cells were cultured in the presence of 800 pg/mL of G418. and resistant cell clones were selected, and tested for core 2 GlcNAc T activity in culture medium. The representative clone 614 C2 showed stable expression of core 2 WO 99/64378 PCT/CA99/00550 - 23 GlcNAc-T activity, and was selected for enzyme production. The cells were routinely propagated in MEM medium containing 5% Fetal Bovine Serum and G418 (0.2 mg/mL). lgG-Sepharose Fast FloWTm beads (Pharmacia Biotech) were added in a ratio of 5 pl of a 50% bead slurry, 2.5 p.l of 2 M Tris9HCl pH 8.0, and 5 pl of 10% Tween-20 per mL of culture medium. Following incubation on a rocking 5 platform at 4'C for 20 h, the beads were collected by centrifugation, washed with 10 volumes of TST buffer (50 mM Tris*HCI pH 8.0. 150 mM NaCl, 0.05% Tween-20) and 2 volumes of 5 mM NH 4 Ac pH 5.0. The recombinant ProtA-core 2 GIcNAc-T enzyme was then eluted with I volume 0.5 M acetic acid pH 3.4 and resuspended in 3 volumes of 0.5 M MES pH 7.5 (Calbiochem). One pU of enzyme activity is defined as the amount of protein forming I pmol/min of reaction product. 10 Solid phase Core 2 GlcNAc-T assay: A stock solution of the core 2 acceptor glycopolymer 3 was prepared by re-suspending the acceptor in water to a concentration of 1.25 mg/mL and then incubating the solution at 60'C for I h. The solution was gently mixed at 15 min intervals during this time to allow the polymer to unwind and become fully dissolved. The glycopolymer solution was not vortexed since strong agitation may cause shearing of the polymer backbone. Sodium azide (0.05%) was added 15 as a preservative and the stock solution of glycopolymer was stored at room temperature. Wallac 96 well Printed Rigid Sample Plates (1450-511; Wallac, FI) were used in all cases for the solid phase assay. To prepare the plates for coating with acceptor, the wells were washed twice with 100 pI of methanol and then rinsed 3 times with 200 pl of water. After allowing the plates to dry at room temperature, the wells were coated with acceptor by adding 60 ul of a 33.3 pg/mL of glycopolymer 20 solution and incubated overnight at room temperature. Following the incubation, unbound glycopolymer was removed by washing 3 times with 200 pl water and the remaining liquid in wells was allowed to evaporate by incubating the plates at 37'C (or room temperature) for approximately 1 h. Dried-coated plates could be used immediately or sealed and stored for use at a later date. The HTS core 2 GlcNAc-T assay consisted of 20 pl of test compound, 20 pl of 3x assay 25 buffer consisting of 90 mM MES pH 6.7. 10 mM EDTA (Sigma), 0.0075 mM UDP-GlcNAc (Sigma) and 0.1 pCi of UDP-[ 3 H]GlcNAc (16 Ci/mmol; Toronto Research Chemicals) and 20 pl of recombinant core 2 GlcNAc-T (containing 8-10 pU/pl) per reaction in 96 well plates. To minimize pipetting, the enzyme and the 3x buffer were routinely combined and 40 pl of the enzyme-buffer mix was added to the wells following the addition of the test compounds. After incubating the plates at 30 25*C for 60 min, the reactions were stopped by adding 175 pl of water to each well, aspirating the contents and washing 4 times with 190 pl water. The radioactive signal was measured using a MicroBeta plate counter (Wallac. FL) after adding 100 pl of OptiPhase Supermix scintillation cocktail (Wallac) to each well and incubating for >2 h, to allow for mixing. Each plate in HTS had 4 controls with vehicle added rather than test extracts, and background was determined with the omission of 35 enzyme, also 4 wells per plate. Background was subtracted for each plate, and HTS results were expressed as a percentage of control reactions on the plate. The HTS assays were run on a Beckman integrated robotic platform using a Biomek 200 pipetting station and Zymark rotating robotic arm. PanLabs (Seattle. WA) supplied a collection of 30,000 bacterial and fungal extracts in 96 well plates.

WO 99/64378 PCT/CA99/00550 - 24 The dried extracts were resuspended in DMSO, and diluted into water at 0.15% DMSO for the core 2 GlcNAc-T HTS. Solution Phase core 2 GIcNAc-T assays. The core 2 GlcNAc-T solution phase assay mixture was similar to that used in earlier studies (Yousefi et al., J.Biol.Chem. 266:1772-1783, 1991; Williams et 5 al., J.Biol.Chem. 255:11253-11261, 1980) but was adapted for automation on the Beckman robotic platform. For HTS assays, 10 pl of test extract, 10 p1 of 3x assay buffer (90 mM MES pH 6.7, 10 mM EDTA, 3 mM Galpl-3GalNAca'-pNp as acceptor, 3 mM UDP-GlcNAc (Sigma) and 0.1 pCi of UDP

[

3 H]GlcNAc (16 Ci/mmol; Toronto Research Chemicals), and 10 p1 of recombinant core 2 GlcNAc-T enzyme (4-5 pU activity) was added to wells of the titre plate. Reactions in a total volume 30 pl were 10 incubated for 1-2 h at 37 0 C and stopped by adding 200 pl cold water. Plates were processed immediately or stored at -20"C. To recover the product, the assay mix was aspirated through C18 packed pipette tips (BGBS96C18 Biotips

T

, National Scientific) and the packing was then washed 3 times with 200 ui of HO. Bound product was eluted into B-scintillation counting plates (Wallac 96 well Printed Rigid Sample Plate: 1450-51 1) by washing the C18 packing 3 times with 100 pl of 100% 15 ethanol. The eluates were then dried overnight at room temperature to remove the ethanol and the radioactive signal was counted in a p-scintillation counter after the addition of counting fluid. Reaction products were found to accumulate in a linear manner for up to 2 hours of incubations. The C18 packed tips were cleaned and regenerated following the processing steps by washing once with 200 pl ethanol and then 3 times with 100 pl of H)0. 20 RESULTS Glycopolymers for solid-phase glycosyltransferase assays: The disaccharide acceptor GalBI-3GalNAca-R where R is either octylmethyl or paranitophenyl has been used routinely in solution core 2 GlcNAc-T assays where UDP-[ 3 H]GlcNAc is the sugar-nucleotide donor. The product, GalBJ1-3([H]GIcNAcBl-6)GalNAca-R is captured on CIg 25 solid support, eluted with ethanol, and measured in a B-counter ( Yousefi et al, J.Biol.Chem. 266:1772 1783, 1991). This procedure has been miniaturized and automated, but remains relatively slow compared to high throughput (HTS) ELISA-style assays. The glycopolymers with GaBil-3GalNAca groups were prepared by chemical synthesis and reacted with recombinant ProtA-core 2 GlcNAc-T to establish the condition for the solid-phase glycosyltransferase assays. The water-soluble glycopolymer 30 acceptors (3-8, 10, and 11-14 Figure 9) used in the solid-phase glycosyltransferase assay are polyvalent substrates composed of N-substituted polyacrylamide backbones containing one disaccharide Gal 1 3GalNAca-O(CH 2

)

3

S(CH

2

)

2 (2) or trisaccharide [GlcNAc( I-2)]Man( I-6)Glc( -O(CH 2

)

3

S(CH

2 )) residues for every ten acrylamide backbone monomers. The viscosity-average molecular weight M, of the core polymer was determined to be 42.1 kDa based on polyacrylamide derived from 1 by treatment 35 with aqueous ammonium alone. The ratio of sugar to acrylamide of one to ten was determined using high field 'H-NMR spectroscopy and was based on previous optimization experiments using analogous glycopolymers in enzyme-linked lectin assays (ELLA) (Roy, Trends in Glycoscience and Glycotech. 8:79-99 1996). The copolymer backbones were modified with various alkylamines to enhance their WO 99/64378 PCT/CA99/00550 - 25 lipophilicity and thus, increase their adsorption behaviors to the surface of the polystyrene microtiter plates. Copolymers 6 and 14, having the most lipophilic N-propylacrylamide backbones, were about eight times more sensitive than either N-ethyl (5, 13) or acrylamide (3, 11) copolymers while 5 copolymers 4 and 12, having an N-methyl substituent, were the least effective coating acceptor. Copolymer 10, containing a shorter allyl spacer was also found unsuitable for the enzymatic glycosylation, presumably because of the inaccessibility of the GaINAc residues in the enzyme's active site. Similarly, copolymers 7 (co-biotin) or 8 (co-methacrylamide) provided either poor coating or poor enzymatic glycosylation. Biotin-containing copolymer 7 was initially designed to serve as coating 10 substrate after capture by streptavidin/avidin pre-coating. Glycopolymer 6, having the most lipophilic N-propylacrylamide backbone, was about eight times more effective than either N-ethyl (5) or acrylamide (3) glycopolymers while glycopolymer 4, having an N-methyl substituent, was the least effective coating acceptor. Coating plastic wells with glycopolymer. Early in the development of the solid-phase assay, variable 15 results were observed with different batches of plastic plates. A number of pre-wash solutions were tested for their ability to improve the consistency of the core 2 GIcNAc-T reaction. Pre-washing the plastic with organic solvents improved the signal by 2-4 fold and eliminated variability between different lots of plates. Washing with non-ionic detergent reduced reaction efficiency. Based on these results, the 96 well plastic plates were routinely washed twice with methanol, then twice with water and 20 stored dry prior to coating with the glycopolymer 3. Washing of plastic plates was performed on the Beckman 2000 workstation with robotic arm. The time and temperature dependency for coating the wells with glycopolymer was determined, and overnight coating with 2 l.g/mL at 20"C was determined to be optimal. Glycopolymer 3 was determined to be in excess, as the recovered solution of polymer was used to coat wells subsequently, and produce 80-90% of the reaction product realized with the first 25 coating. However, glycopolymer solutions were routinely used only once. Characterization of the Core 2 GlcNAc-T solid-phase assay In the initial experiments, 96 well plates were coated with a solution of 2 pg/well of glycopolymer acceptor 3, and the reaction products were observed to be proportional to added enzyme over 60 minutes. However, the Km for UDP-GIcNAc, and for acceptor using ProtA-core 2 GIcNAc-T in the solution assay was determined to be 1.75 mM and 30 146 pM respectively. In contrast, the solid-phase glycosyltransferase reaction conditions employ substrates well below Km concentrations, as the amount of glycopolymer 3 bound to the plastic is limiting. Therefore, the sugar-nucleotide concentration is adjusted to optimize the detection of radioactive product and is also below Km concentrations. To establish that the substrates are not exhausted during the 60 minute reaction, a time course and titration of UDP-GlcNAc was performed at 35 37*C. At higher concentrations of UDP-GIcNAc, the reaction went to completion in less than 5 minutes. However, with UDP-GIcNAc at 2.5 ptM, and 200 pU of enzyme activity, the core 2 GIcNAc T reaction product accumulated in a time-dependent manner for 30-60 minutes. The maximal product formed was 6-10 pmoles per well, and when 2.5 pM UDP-GIcNAc was used in the reaction, this represented approximately 4% utilization of the sugar-nucleotide donor. To simplify the HTS WO 99/64378 PCT/CA99/00550 -26 protocol, these conditions (2.5 pLM UDP-GlcNAc, 200 pU enzyme) were then further tested at room temperature (approximately 20 0 C). Under these conditions, product accumulation was found to be linear with time for approximately 60 min. and thus, the H4TS assay was routinely performed at room temperature. 5 Glycopolymer acceptors for GlcNAc-TV were also made and tested using recombinant enzyme (Figure 10). Similar to that observed for core 2 GlcNAc-T, glycopolymer 14, with the most lipophilic N-propylacrylamide backbone more effective than either N-ethyl (13) or acrylamide (11) glycopolymers. Glycopolymer 12, an N-methyl substituent linker was the least effective coating acceptor. The GlcNAc-TV reactions product using glycopolymer 14 accumulated in a time and enzyme 10 dependent manner. Core 2 GlcNA c-Thigh-throughput screen (HTS) of microbial extracts. A microbial library of 30,000 extracts was subjected to HTS using the core 2 GIcNAc-T solid-phase assay as the primary screen (ie. glycopolymer 3). Normalized results from a typical run of 1,600 assays are shown in Figure 11. The signal to noise was 20-fold and the CV of the positive controls was ±9.4 % assay. A series of 48 hit 15 extracts, chosen from the total primary screen data (ie. >50% inhibition) were placed on plates with 88 other inactive extracts. and re-tested in a 5 point dilution series using both the solid-phase and solution core 2 GIcNAc-T assays. 94.4 % (17/18) of the hits identified in the solution assay were also hits in the solid phase assay. Additional hits, 3 with good and 8 with inconclusive titration curves were observed in the solid-phase assay. Active extracts identified in the core 2 GlcNAc-T HTS can be fractionated to 20 identify active molecules for further testing in cell culture and animal models of disease. DISCUSSION A solid phase glycosyltransferase assay was optimized for use with recombinant core 2 GIcNAc-T. The assay was also tested with glycopolymer acceptors for GlcNAc-TV and GIcNAc-TI and shown to be acceptable for other glycosyltransferase enzymes. The solid-phase core 2 GIcNAc-T 25 assay was used in a HTS of a library of microbial extracts and active extracts were confirmed with a high degree of concordance in the solid-phase and a conventional solution assay. The solid-phase assay format allowed 5-6 fold increase in throughput compared to a solution phase assay, for a rate of 7,500 per day. The core 2 GIcNAc-T HTS of 30,000 microbial extracts yielded hits at a frequency of 1.5% in 30 the solution assay. One third of the library was also screened using the solid phase assay and yielded a high degree of concordance with the results previously found with the solution assay. EXAMPLE 3 High Throughput L-PHA Assay Materials and Methods 35 Chemicals. L-PHA, Triton X-100 and para-nitrophenylphosphate were obtained from Sigma; diethanolamine was purchased from Fisher. Cells. The origin and properties of the DBA-2 strain lymphoreticular tumor MDAY-D2 have been previously described (Kerbel, RS, Florian, M, Man, MS, Dennis, J and McKenzie IF (1980) J.Natl.Cancer Inst., 64, 1221-1230). Cells were cultured in a-modified Eagle's medium containing 2% WO 99/64378 PCT/CA99/00550 - 27 heat-inactivated fetal calf serum (Gibco BRL) at 37'C in a 95%O,/5%CO humidified atmosphere. Alkaline phosphatase assay. Determinations were carried out using 96-well plates. Each well contained a variable number of MDAY-D2 cells maintained in 125 Il of culture medium supplemented with 2% fetal calf serum. The alkaline phosphatase reaction was initiated by adding 75 tl of assay 5 mixture (I M diethanolamine buffer, pH 9.8, 2 mM MgCl,, 1% Triton X-100 and 2.5 mM para 0 nitrophenylphosphate) and incubated at 37 C for up to 90 min. The reaction was stopped with 80 p.l of 3.5 M NaOH. After 15-30 min of colour development, absorbance of the chromogenic product para nitrophenol was measured at 405 nM using a multiwell scanning photometer (Thermomax Multiplate Reader, Molecular Devices). Background values were determined through assays performed on culture 10 medium alone in the absence of cells and routinely subtracted. Linearity between the absorbance at 405 nM and concentration of para-nitrophenol was in the range 0-2.5 (S = 17.23 mM'cm'). Screening via L-PHA assays. The procedure was completely automated by using a robotic workstation (Biomek 2000, Beckman) capable of processing nine 96-well plates simultaneously. Determinations were performed in flat bottom 96-well plates (88 samples + 8 controls per plate). Each well (columns 15 1-11) received 10 il of compound (in 2.5% DMSO), while 10 ul of 2.5% DMSO in water was added to column 12. All 96 wells received 5x10 MDAY-D2 cells in 90 pl culture medium supplemented with 2% FCS. After 16-20 h incubation at 37 C, 25 pl of L-PHA (100 pg/mL in culture medium) was added to the first I I columns and to 4 wells of the 12th (positive control). The other 4 wells received 25 pl of medium supplemented with 2% FCS (negative control). Assay plates were maintained for 30-36 h at 20 37*C, and alkaline phosphatase activity was measured according to the protocol described above using an incubation time of 1 h. Cell density was subconfluent throughout the course of the assay. Proliferation indices were expressed as percentage values, calculated with the formula: Normalized Signal = (A 405 of sample - mean A 405 positive control)/(mean A 4 o 5 negative control - mean 25 A 405 positive control) RESULTS In homogeneous screening assays the results are determined without washing or transferring target proteins or cells, reactants, and test compounds from the assay plates. Homogeneous assay 30 formats save time in performing the assay, and with less manipulation, the low errors are observed. This translates into fewer follow-up assays on putative hits in a large screen. A homogeneous cell based assay has been developed that measures cell growth and variability using endogenous alkaline phosphatase activity. MDAY-D2 tumor cells maintained in tissue culture in log phase of growth exhibit alkaline 4 35 phosphatase activity in the range 40-80 nmol/h/10 cells. Alkaline phosphatase measurements were linear over time for at least 90 min, and directly proportional to cell number, allowing detection of 1500 cells. MDAY-D2 doubling time calculated through accumulation of alkaline phosphatase activity WO 99/64378 PCT/CA99/00550 - 28 was -14h. similar to that measured by counting cells. The alkaline phosphatase assay is comparable in reproducibility and sensitivity, with a commercially available, chemiluminometric method. The apparent Km of alkaline phosphatase measured in the MDAY-D2 whole cell assay was 0.86 mM, whereas the value exhibited by the soluble enzyme present in fetal calf serum was 0.21 mM. 5 Background activity present in culture medium containing 2% FCS produced an A 405 of 0.2 after lh of incubation and represented approximately 10% of the signal with the standard assay conditions. Swainsonine blocks a-mannosidase II, acting as an inhibitor of complex-type N oligosaccharide biosynthesis resulting in resistance to the toxicity of L-PHA lectin. Swainsonine protected MDAY-D2 cells from L-PHA toxicity with an IC 50 value of 0.0528 +/- 0.0087 IM (n =8). 10 An IC 50 value of 0.2 pM was previously reported using thymidine incorporation as a measure of cell growth (Dennis et al, 1993, Biochem. Pharmacol., 46, 1459-1466). The alkaline phosphatase cell assay was applied to high-throughput screening of a microbial extract library. The signal to noise ratio (i.e. growth of L-PHA-treated/control MDAY-D2 cells) was 5 and the coefficient of variation of both negative and positive control samples was 4.2% and 2.4%, 15 respectively. Twenty microbial extracts of the 30,000 tested increased cell viability in the presence of L-PHA to a degree greater than 3xSD of the mean. These fell on the right-hand side of normal distribution Figure 12). On re-testing, 4 of the 20 extracts were confirmed as hits for further fractionation. A number of extracts suppressed growth below that observed in the presence of L-PHA (i.e. left of the normal distribution). These likely contain compounds that are generally toxic, and not of 20 interest. DISCUSSION The proliferation rate of MDAY-D2 cells was monitored by employing an assay of alkaline phosphatase activity. The motivation for this work was to establish a simple, reproducible and cost effective procedure to be applied for high throughput screenings via L-PHA assay. A colorimetric 25 determination of alkaline phosphatase activity has been found suitable to measure lymphokine dependent B cell proliferation (Hashimoto N and Zubler RH (1986) JImmunol.Methods 90, 97-103.); the advantage of the protocol described herein is that the method can be carried out in a single step, without removal of the culture medium or cell pelletting and washing, thereby permitting fully automated procedures. Furthermore, use of a robotic platform allowed simultaneous processing of 30 thirty-six 96-well plates. The method is very cost-effective, especially when compared to other commercially available assay kits. Sensitivity and accuracy of the alkaline phosphatase method are based upon several observations: i) MDAY-D2 cells express relatively high levels of enzyme, whereas background activity present in fetal calf serum (2%) is low; ii) readings of A 40 5 were found to be proportional to the 35 concentration of reaction product: iii) the reaction is linear with time within a relatively wide interval of up to 1.5h; and, iv) the numbers of MDAY-D2 cells (both untreated and L-PHA-treated) correlated 3 5 with enzyme activity within a relatively wide range (i.e. lxI0 up to 2.5x10 cells). The assay was performed using ImM substrate (final concentration), 4-fold above the Km of the serum enzyme (i.e. 0.21 mM) and similar to that of the cellular enzyme (i.e. 0.86 mM). With this 4-fold difference in Km WO 99/64378 PCT/CA99/00550 - 29 values, the signal to background ratio may be amplified by increasing the substrate concentration above ImM. The assay was proven reliable by several indicia. For example, when swainsonine, a known inhibitor of N-linked oligosaccharide processing, was employed in conjunction with the L 5 PHA/alkaline phosphatase assay, the IC 50 of the drug compared well with that previously reported using thymidine incorporation to measure cell growth. Additionally, the results of the cell proliferation measurements corresponded to those obtained using another single-step, commercially available chemiluminometric kit. Finally, during the screening of extract libraries (30,000 samples), control measurements of alkaline phosphatase activity (n=3200) showed coefficient of variations which were 10 markedly low. While the present invention has been described with reference to what are presently considered to be the preferred examples, it is to be understood that the invention is not limited to the disclosed examples. To the contrary, the invention is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims. 15 All publications, patents and patent applications are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety.

WO 99/64378 PCT/CA99/00550 - 30 Table I Enzyme Donor Acceptor Glycoprotein-fucosylgalactoside UDP D-GaINAc Glycoprotein a-L fucosyl-(1,2) alpha-N- D-galactose acetylgalactosaminyltransferase (EC 2.4.1.40) (N-acetylneuraminyl)- UDP D-GaINAc (N-acetylneuraminyl)D galactosylglucosylceramide N- galactosyl - D-glucosylceramide acetyl galactosaminyltransferase (EC 2.4.1.92) P-1,4-N-acetyl galactosaminyl UDP D-GaINAc (N-acetvineuraminvl)D transferase (murine T- galactosyl-D-R lymphocyte CT antigen synthesis) (Swiss Prot Q09199) N-acetyllactosaminide alpha-1,3 UDP-D-Gal p-D-galactosyl-(1,4) galactosyltransferase (galactosyl N-acetyl-D-glucosaminyl-R transferase) (EC 2.4.1.15 1) Glycoprotein-fucosylgalactoside UDP-D-Gal Glycoprotein a-L fucosyl (1,2) -a -galactosyltransferase D-galactose (EC 2.4.1.37) N-acetyllactosamine synthase UDP-Gal N-acetyl-D-glucosamine (EC 2.4.1.90) 2-hydroxyacyl sphingosine I- - UDP-Gal 2-(2-hydroxvacyl) sphingosine galactosyltransferase (EC 2.4.1.45) UDP-galactose-glucose UDP-D-Gal D-Glucose galactosyltransferase N Acetyllactosamine synthase Fucosylglycoprotein a-N- UDP-D-GalNAc Glycoprotein a-L-fucosyl acetylgalactosaminyl transferase (1,2)-D-galactose Galactoside-2-L-fucosyl GDP-L-fucose -D-galactosyl-R transferase (EC 2.4.1.69) galactoside 3(4)-L fucosyl - GDP-L-fucose 1,3-p-D-galactosyi N- acetyl-D transferase (EC 2.4.1.65); glucosaminyl-R fucosyltransferase 6 (SWISS PROTP51993); fucosyltransferase 5 (SWISS PROT QI 1128) a-1,3-mannosyl-glycoprotein UDP-D-G IcNAc a-D-mannosyl-1,3 (Ri)- P-D 3-1.2 N-acetylglucosaminyl mannosyl-R2 transferase (GnT 1) (EC 2.4.1.10 ) WO 99/64378 PCT/CA99/00550 -31 Enzyme Donor Acceptor a- 1,6-mannosyl-glycoprotein-3 UDP-D-GIcNAc a-D-mannosyl- 1,6 (N-acetyl 1,2 N-acetylglucosaminyl p-D glucosaminyl-1,2--a- D-( transferase (GnT II) (EC mannosyl-1.3-)-p-D- mannosyl 2.4.1.143) R a-1,3(6)-mannosylglycoprotein P UDP-D-GIcNAc N-acetyl-p-glucosaminyl- 1,2 1,6-N-acetyl-glucosaminyl alpha-D-mannosyl- 1,3(6)-(N transferase (EC 2.4.1.155) (GnT acetyl-p-D-glucosaminyl-I,2-a V) D-mannosyl- 1,6(3)-PD mannosyl- 1,4-N-acetyl-p-D glucosaminvl-R Polypeptide-N- UDP-D-GaINAc Polypeptide acetylgalactosaminyl transferase (EC 2.4.1.41) -,4-mannosvl-glycoprotein p- UDP-D-GIcNAc N-acetyl-P-D-glucosaminyl-1,2 1,4-N-acetylglucosaminyl alpha-D-mannosyl- I ,3-(N-acetyl transferase (GnT I1) (EC p-D-glucosaminvi- 1.2-a-D 2.4.1.144) mannosyl- I,6)-p-D-mannosyl 1,4-N-acetyl-p-D-glucosaminyl R Chitin synthase (EC 2.4.1.16) UDP-D-GlcNAc (1,4)-(N-acetyl-P-D glucosaminvi)} (N) p-I,3-galactosyl-O-glycosyi UDP-D-GlcNAc p-D-galactosyl- 1,3 N glycoprotein-3 1,6-N I acetyl-D-galactosaminyl-R acetylglucosaminyltransferase (EC 2.4.1.102) (P1,6 (0-linked, core 2)) UDP-N-acetylglucosamine- UDP-D-GIcNAc I Dolichyl phosphate dolichyl-phosphate N-acetyl glucosaminephosphotransferase (EC 2.7.8.15) Galactoside 3-fucosyltransferase GDP-L-fucose 1.4-p-D-galactosyl-N-acetyl-D (EC 2.4.1.152) glucosaminyl-R Fucosyltransferase 7 (SWISS GDP-L-fucose a-2,3-Neu-N-acetyl- 1,4-p-D PROT Q 1130) galactosyl-N-acetyl-D glucosaminyl-R WO 99/64378 PCT/CA99/00550 - 32 Table 2 3-deoxy-D-manno-octulosonic acid (KDO) transferase Chlamydia pneumoniae KDO transferase gb:z31593 5 Chlamydia psittaci KDO transferase gb:x80061 Chlamydia psittaci gseA transferase gb:x69476 Chlamvdia trichomatis KDO transferase gb:m64618 Chlamydia trachomatis gseA transferase gb:z22653 gb:z22654 gb:z22655 gb:z22656 gb:z22659 10 Escherichia coli kdtA gb:m60670 gb:m86305 gb:u00039 sw:p23282 (kdta-ecoli) Haemophilus influenzae kdtA gb:145293 gb: u32 748 sw:p44806 (kdtahaein) O-antigen Gal-2--fucosyltransferase Yersinia enterocoliticafucosyltransferase gene gb: u18674 gb:u25113 gb:u46859 cid (chain length determining) (similar to putative undecaprenyl-P--GIcNAc transferase) 15 Escherichia coli cidi gb:z17241 sw:q05032 (cldiecoli) Escherichia coli c/d2 gb:m89934 sw.p35272 (cId2_ecoli) Salmonella typhimurium cid gb:z17278 sw:q04866 (cld salty) Shigellaflexneri cldgb:x71970 sw:p37792 (cld_shifl) cpsD galactosyltransferase 20 Streptococcus agalactiae cpsD gene gb:109116 IgtA galactosyltransferase Rhizobium leguminosarum Allaway et al (1996) unpublished gb:x94963 murG N-acetylglucosaminyltransferase Bacillus subtilis murG gene gb:s56399 gb:x64259 25 mraY phospho-N-acetylmuramoylpentapeptide synthase EC 2.7.8.13 Bacillus subtilis mraY gene gb:z 15056 sw:q03521 (mravbacsu) Escherichia coli mraY gene gb:x51584 gb:x55034 gb:d10483 sw.p15876 (mray ecoi) mtfA, mtfB, mtfC mannosyltransferases Escherichia coli mtfA, mtfB and mtfC genes gb:d13231 gb:d43637 30 neuS 2,8-sialy/transferase Escherichia coli neuS gene gb:x60598 nodC N-acetylglucosaminyltransferase Azotorhizobium caulinodans gb:118897 sw:q07740 (nodcazoca) Bradyrhizobium elkanii gb:u04609 35 rfaB 1,6-galactosvltransferase Escherichia coli rfaB gene gb:m80599 gb:u00039 sw:p27127 (rfab ecoli) Salmonella typhimurium rfaB gene gb:s56361 sw:q06994 (rfab salty) rfaC heptulosyltransferase 1 Escherichia coli rfaC gene gb: u00039 sw:p241 73 (rfac-ecoli) 40 rfaG glucosyltransferase Escherichia coli rfaG gene sw:p25740 (rfagecoli) rfal 1,3-galactosyltransferase EC 2.4.1.44 Escherichia coli rfal gene gb:m80599 gb:u00039 sw:p27128 (rfai-ecoli) Salmonella typhimurium rfal gene gb:x53847 sw:p19816 (rfai salty) WO 99/64378 PCT/CA99/00550 - 33 Table 2 Cont'd rfaJ 1,2-glucosyltransferase EC 2.4.1.58 5 Escherichia coli rfaJ gene sw:p27129 (rfajecoli) Salmonella typhimurium rfaJ gene sw.p19817 (rfajsaltv) rfaK 1,2-N-acetylglucosaminyltransferase EC 2.4.1.56 Escherichia coli rfal gene gb:u00039 sw:p2 7242 (rfai ecoli) ribF galactosyltransferase 10 Campylobacter hvoilei rjbF gene gb:x91081 Klebsiella pneumoniae rfbF gene gb:131762 gb:141518 rfbN rhamnosyltransferase Salmonella typhimurium rJbN gene gb:x56793 rfbP galactosyltransferase 15 Yersinia enterocolitica rJbP gene gb:u18674 gb:u25113 gb:u46859 Salmonella enterica rJbP gene gb:x61917 rfbQ rhamnosyltransferase Salmonella enterica rfbQ gene gb:x61917 rfbU mannosyltransferase 20 Salmonella tvphimurium rJbU gene gb:x56793 sw:p26402 (rJbusalv) rfbW second mannosyitransferase Salmonella enterica rjbW gene gb:x61917 rfbZ first mannosyltransferase Salmonella enterica rJbZ gene gb:x61917 25 rfe undecaprenyl-P--GIcNAc transferase Escherichia coli rfe gene gb:s75640 gb:m87049 gb:m 76129 sw:p24235 (rfeecoli) Mycobacterium leprosum rfe gene gb:u15186 sw:p45830 (rfemycle) rffM probable N-acetyl-D-mannosaminuronic acid transferase Escherichia coli rfJM gene gb:m87049 sw:p27836 (rffmecoli) 30 Salmonella typhimurium rffM gene gb:m95047 sw:p3 7457 (rffmsalty) rffT probable 4--fucosyltransferase Escherichia coli rfjT gene gb:m8 7049 sw:p2 7835 (rfftecoli) Salmonella tvphimurium rffT gene gb:m95047 sw:p3 7458 (rfftsaltv) RhIAB rhamnosyltransferase 35 Pseudomonasaeruginosa rhIAB gene gb:128170 Glycosyltransferase locus of N. gonorrhoeae U.S. Patent No. 5,703.367 to Gotschlich WO 99/64378 PCT/CA99/00550 -34 Table 3 0 9 'NH COOH R-tH 0CN",0 No. R R H A -NHCOR' -CHRWR H -(CH 2

)

2 F B -NHCOR' -CHR 3 R 4 H -CH ,-OCH 3 C -NHCR' -CR 3

R

4 D -NHCOR' -CHR 3

R

4 H -(CH 2 ) -N E -NHCOR' -CHR 3 R 4 H -CH 2

N(CH

3

)CH

2

CH

2 F F -NHCOR' -CHR 3

R

4

-NH

2 F G -NHCOR' -C(CH- 3

)(NI-

2 )CH2- OCH 3 H -NHCOR' -CHR 3

R

4

-NH

2 M -NHCOR' -CHR 3

R

4

-NH

2

-CH

2

N(CH

3

)CH

2

CH-

2 F J -NHCOR' -CHR'R 4

-NH

2 HNC3O U. -NHCOR' -CHR"R4 H -N(CH 3

)CH

2

CH

2 F V -NHCOR' -CHR 3 R 4 H CH)- I WO 99/64378 PCT/CA99/00550 - 35 Table 4 H

OS

3 HI R-IH 0 CN~ No. iR IR' R K -NHCOR' -CHR 3 R' -NH, /C H 3 L -NHCOR 1

-IIR

3 R' -NH, 1F M -CHR 3 R' -NH, N -NHCOR' -CHiR 3 R' -NH 2 -CH4,N(C 2

H

5 )CHCH(CH3)OH 0 NHCOR' -CHR 3

R

4 -H -CH,NHCOCH(CH 3

)

2

,

WO 99/64378 PCT/CA99/00550 - 36 Table 5 SOH "N.NH II

(CH

2 )q I R-CH 0 N q =O0or I No. R R jR P -NHCOR' -CHR 3

R

4

-NH

2 H Q -NHCOR' -CHR 3 R 4 -NH 2 F R

-CHR

3 R 4

-NH

2 -NHCOR'

OCH

3 S -NHCOR' -CHR 3 R 4

-NH

2

-CH

2

N(C

2 Hs)CH 1

CH(CH

3 )OH T -NHCOR' -CHR 3 R 4

-NH

2 -- CH 2 NHCOCH(CH3) 2

Claims (11)

1. A combinatorial library comprising a predetermined collection of nucleoside peptide molecules for inhibiting the transfer of a sugar from a selected sugar nucleotide donor to a selected acceptor by a carbohydrate processing enzyme wherein a nucleoside peptide molecule comprises (a) a 5 nucleoside monomer; (b) a spacer monomer coupled to the nucleoside monomer wherein the spacer monomer comprises one or more amide linked amino acid residues or mimetics thereof; and (c) cap monomers attached to the spacer monomer; wherein the nucleoside peptide molecules differ from each other as to the identity of at least one element of the nucleoside monomer, spacer monomer or cap monomers. 10 2. A combinatorial library as claimed in claim I wherein the carbohydrate processing enzyme is a glycosyltransferase involved in the biosynthesis of glycoproteins, glycolipids, or glycosyl phosphatidyl inositols.

3. A combinatorial library as claimed in claim 2 wherein the carbohydrate processing enzyme is an N-acetylglucosaminyltransferase I, II, II, IV, or V, or p-1,3-galactosyl-O-glycosyl-glycoprotein P 15 1,6-N-acetylgucosaminyl transferase (core 2 GlcNAc).

4. A combinatorial library as claimed in claim 1, 2, or 3 wherein the nucleoside monomer is uridyl, 2'-deoxyuridyl, or 5'-amino-5'deoxy-2',3'-0-isopropylidine uridyl.

5. A combinatorial library as claimed in any one of the preceding claims wherein the cap monomer is methyl (Me), formyl (CHO), ethyl (Et), acetyl (Ac), t-butyl (t-bu), anisyl, trifluoroacetyl (Tfa), 20 benzoyl (Bz), 4-methylbenzyl (Meb), thioanizyl, thiocresyl, benzyloxymethyl, 4-nitrophenyl (Pnp), benzyloxycarbonyl (Z), 2-nitrobenzoyl (NBz), 2-nitrophenylsulphenyl (Nps), 4 toluenesulphonyl (Tosyl, Tos), pentafluorophenyl (Pfp), diphenylmethyl (Dpm), 2 chlorobenzyloxycarbonyl (CI-Z), 2,4,5-trichlorophenyl, 2-bromobenzyloxycarbonyl (Br-Z), triphenylmethyl (Trityl, Trt), 2,2,5,7,8-pentamethyl-chroman-6-sulphonyl (Pmc), t 25 butyloxycarbonyl (Boc), benzyl (Bzl), benzyloxymethyl (Bom), and 9-fluorenylmethyloxycarbonyl (Fmoc).

6. A combinatorial library as claimed in any one of the preceding claims wherein the spacer monomer is a single amide linked amino acid, an amide linked dipeptide, or an amide linked tripeptide, or a mimetic thereof. 30 7. A nucleoside peptide molecule comprising a nucleoside monomer; a spacer monomer coupled to a nucleoside monomer, wherein the spacer monomer comprises one or more amide linked amino acid residues, or a mimetic thereof; and cap monomers attached to the spacer monomer.

8. A nucleoside peptide molecule of the formula I: O 35 x I -NH R CH 0 I P WO 99/64378 PCT/CA99/00550 - 38 where X is H, -COOH, -OSO 3 H, or (CH 2 )qSO 3 H where q is 0 or 1. and R represents (Y)m where Y is an amide linked amino acid residue and m is 1-3, Z' and Z are the same or different and represent hydroxyl or alkoxy, or Z' and Z together form an acetonide group, and wherein free NH 2 groups in the 5 compound of the formula I are capped with a cap monomer.

9. A nucleoside peptide molecule of the formula I as claimed in claim 8 wherein X is H, -COOH, -OSO 3 H, or (CH 2 )qSO 3 H where q is 0 or 1, Z and Z' are both hydroxyl or together form an acetonide group, R represents -NHCOR', wherein R' represents 10 (a) -C(CH 3 )(NH 2 )CHr - R2, wherein R 2 is alkoxy; or (b) -CHR3R 4 wherein R 3 is hydrogen or -NH, and R 4 is R 5 wherein R 5 is 15 halogen, alkyl, or alkoxy, , -CH 2 N(CH 3 )CH 2 CH 2 R 6 or - N(CH 3 )CH 2 CHR 6 wherein R 6 is halogen, 20 0 -CHN(CH3)CO- L, -CH 2 N(C 2 Hs)CH 2 CH(CH 3 )OH, or -CH 2 NHCOCH(CH 3 ) 2 , or R 4 represents (CH 2 )nRg wherein n 0 to 5, R' is halogen, / \ R 9 wherein R 9 is 25 alkoxy, , -N -N(CH 3 )CH 2 CH 2 R' 0 wherein R' 0 is halogen, -N(C 2 HS)CH 2 CH(CH 3 )OH, or -NHCOCH(CH 3 ) 2 and wherein free amino groups are protected with a cap monomer. 30 10. A nucleoside peptide molecule of the formula I as claimed in claim 8 wherein X is -COOH, and R represents -NHCOR' wherein R' represents -CHR 3 R 4 wherein R 3 is hydrogen and R 4 is (CH 2 )nR' wherein n = 0 to 5, preferably I to 4, R 8 is halogen, T -. R9 wherein R 9 is alkoxy, halogen, or alkyl, 35 -N NR or -N(CH 3 )CHCH 2 R' 0 wherein R' 0 is halogen, -N(C 2 H 5 )CH,CH(CH 3 )OH, or -NHCOCH(CH 3 ) 2 . WO 99/64378 PCT/CA99/00550 -39 I1. A nucleoside peptide molecule of the formula I as claimed in claim 8 wherein . X is -COOH, and R represents -NHCOR' wherein R' represents -CHR 3 R 4 wherein R- represents -NH 2 , and R 4 is Q-R5 wherein R 5 is halogen, alkyl or alkoxy, H 2 C.- -CH 2 N(CH 3 )CH 2 CH 2 R 6 wherein R 6 is halogen, -CH 2 N(C 2 H5)CHCH(CH 3 )OH, CH2NHCOCH(CH 3 ) 2 10 0 or -CH2N(CH3)CO

12. A nucleoside peptide molecule of the formula I as claimed in claim 8 wherein X is -OSO 3 H, or (CH 2 )qSO 3 H where q is 0 or 1, R represents -NHCOR' wherein R' represents -CHR3R 4 wherein R 3 15 represents -NH 2 , and R 4 is OD -R 5 wherein R5 is halogen, alkyl, or alkoxy, -CH 2 N(CH 5 )CH 2 CH(CH 3 )OH, or -CH 2 NHCOCH(CH 3 ) 2 . 20 13. A process for preparing a combinatorial library containing a predetermined collection of nucleoside peptide molecules for inhibiting the transfer of a sugar from a selected sugar nucleotide donor having a heterocyclic amine base, to a selected acceptor by a carbohydrate processing enzyme comprising: (a) coupling one or more amino acids, or mimetics thereof to a nucleoside monomer unit 25 which comprises a heterocyclic amine base coupled to a sugar wherein the base corresponds to the heterocyclic amine base of the sugar nucleotide donor, or a modified form or analogue of the base; and (b) capping any free functional groups or amine groups with a cap monomer unit.

14. A method of using a combinatorial library as claimed in claim 1 for screening for 30 pharmacologically active molecules.

15. A solid-phase bioassay for identifying a compound having inhibitory activity against a carbohydrate processing enzyme which comprises (a) coupling an acceptor for the carbohydrate processing enzyme to a polymer and coating onto a carrier; (b) adding a carbohydrate processing enzyme, a sugar nucleotide donor labeled with a detectable substance, and a test compound; (c) 35 measuring the detectable change produced by the detectable substance; and (d) comparing to a control in the absence of the test compound wherein a decrease in the amount of detectable substance with the test compound indicates that the test compound has inhibitory activity against the enzyme. WO 99/64378 PCT/CA99/00550 - 40 16. A method for identifying a compound that inhibits N-linked oligosaccharide processing comprising (a) reacting a test compound with cells expressing N-linked oligosaccharides in the presence of L-PHA and measuring alkaline phosphatase activity; and (b) comparing to a control in the absence of the compound wherein an increase in alkaline phosphatase activity indicates that the 5 compound inhibits N-linked oligosaccharide processing.

17. A pharmaceutical composition containing a compound identified by a method as claimed in any one of claims 14, 15, or 16.