astilbin (Q4810880)

(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

Astilbin (English)

6 October 2016

2 references

(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

1 reference

(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

2 references

(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

2 references

2 references

(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

1 reference

(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chroman-4-one

1 reference

(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one

1 reference

1 reference

(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one

1 reference

chemical formula

C₂₁H₂₂O₁₁

1 reference

Astilbin (English)

6 October 2016

CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O

1 reference

Astilbin (English)

6 October 2016

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O

1 reference

Phenolic compounds from Hypericum perforatum

Astilbin (English)

6 October 2016

2 references

Flavonoids from Hypericum perforatum show antidepressant activity in the forced swimming test

Vitis vinifera

3 references

Phenolic composition of grape stems

Direct liquid chromatographic analysis of resveratrol derivatives and flavanonols in wines with absorbance and fluorescence detection

Caftaric and coutaric acids in fruit of Vitis

Stelechocarpus cauliflorus

1 reference

Inhibitors of aldose reductase and advanced glycation end-products formation from the leaves of Stelechocarpus cauliflorus R.E. Fr

Desmos cochinchinensis

1 reference

Phenolic constituents with inhibitory activity against NFAT transcription from Desmos chinensis

Mallotus metcalfianus

1 reference

Polyphenols isolated from antiradical extracts of Mallotus metcalfianus.

Petiveria alliacea

1 reference

6-C-formyl and 6-C-hydroxymethyl flavanones from Petiveria alliacea

Andira inermis

1 reference

Andinermals A-C, antiplasmodial constituents from Andira inermis

Astilbe thunbergii

1 reference

Norepinephrine-augmenting lipolytic effectors from Astilbe thunbergii rhizomes

Calliandra haematocephala

1 reference

ANTIBACTERIAL CONSTITUENTS OF CALLIANDRA HAEMATOCEPHALA

Cratoxylum formosum

1 reference

Two xanthones from roots of Cratoxylum formosanum

Drimys granadensis

1 reference

Flavonoid glycosides from Cassia alata

Drimys winteri

1 reference

Isolation and identification of active compounds from Drimys winteri barks.

Engelhardia roxburghiana

3 references

Enhancement of the vanadate-stimulated release of lipoprotein lipase activity by astilbin from the leaves of Engelhardtia chrysolepis

Sweet dihydroflavonol rhamnoside from leaves of Engelhardtia chrysolepis, a chinese folk medicine, hung-qi.

Effect of astilbin in tea processed from leaves of Engelhardtia chrysolepis on the serum and liver lipid concentrations and on the erythrocyte and liver antioxidative enzyme activities of rats

Harungana madagascariensis

1 reference

Two prenylated anthrones in Harungana madagascariensis

Hymenaea martiana

1 reference

Isolation, Chemical Identification and Pharmacological Evaluation of Eucryphin, Astilbin and Engelitin Obtained from the Bark of Hymenaea martiana

Hymenaea parvifolia

1 reference

Casein kinase II inhibitors isolated from two Brazilian plants Hymenaea parvifolia and Wulffia baccata

Hypericum patulum

1 reference

Constituents of Hypericum Montbretii

Iryanthera sagotiana

1 reference

Flavonoids from Iryanthera sagotiana

Lyonia ovalifolia

2 references

Studies on the Constituents of the Leaves of Lyonia ovalifolia DRUDE in Nepal

Studies on the Constituents of Lyonia ovalifolia SIEB. et ZUCC. Var. elliptica HAND.-MAZZ

Rhododendron simsii

1 reference

Flavonoid biosynthesis in petals of Rhododendron simsii

Smilax glabra

3 references

Astilbin selectively induces dysfunction of liver-infiltrating cells--novel protection from liver damage

A new flavanone isolated from rhizoma smilacis glabrae and the structural requirements of its derivatives for preventing immunological hepatocyte damage

Phenolic Glycosides from Rhizomes of Smilax glabra

Bicuiba oleifera

1 reference

Phytochemical and pharmacological investigations of Virola oleifera leaves

Vismia micrantha

1 reference

Constituents of Bridelia micrantha

Dimorphandra mollis

2 references

Aromatic compounds from three Brazilian Lauraceae species

Toxicity of Dimorphandra mollis to Workers of Apis mellifera

Sarcandra glabra

1 reference

Characterization of phenolics of Sarcandra glabra by non-targeted high-performance liquid chromatography fingerprinting and following targeted electrospray ionisation tandem mass spectrometry/time-of-flight mass spectrometry analyses.

Cratoxylum arborescens

1 reference

Anti-HIV-1 constituents from leaves and twigs of Cratoxylum arborescens

Erythroxylum gonocladum

1 reference

ACE inhibition by astilbin isolated from Erythroxylum gonocladum (Mart.) O.E. Schulz

mangosteen

1 reference

Three xanthones and a benzophenone from Garcinia mangostana

Litsea sericea

1 reference

Investigation of Flavonoid Glycosides fromNeolitsea Sericeavar.Auratavia the General Method and HPLC-SPE-NMR

Malpighia emarginata

1 reference

Skin-lightening effect of a polyphenol extract from Acerola (Malpighia emarginata DC.) fruit on UV-induced pigmentation

Neolitsea sericea

1 reference

Investigation of Flavonoid Glycosides fromNeolitsea Sericeavar.Auratavia the General Method and HPLC-SPE-NMR

Neolitsea aurata

1 reference

Investigation of Flavonoid Glycosides fromNeolitsea Sericeavar.Auratavia the General Method and HPLC-SPE-NMR

Smilax bockii

1 reference

Maltol glucosides from the tuber of Smilax bockii

Smilax corbularia

1 reference

Estrogenic and anti-estrogenic compounds from the Thai medicinal plant, Smilax corbularia (Smilacaceae).

Erythroxylum gonoclados

1 reference

ACE inhibition by astilbin isolated from Erythroxylum gonocladum (Mart.) O.E. Schulz

Ochna gamblei

1 reference

7-O-Methyltetrahydroochnaflavone, a new biflavanone from Ochna beddomei

Eucalyptus globulus

1 reference

Phenolic compounds from the branches of Eucalyptus maideni

Eucalyptus maidenii

1 reference

Phenolic compounds from the branches of Eucalyptus maideni

Identifiers

InChI

InChI=1S/C21H22O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-26,28-29H,1H3/t7-,15-,17+,18+,19+,20-,21-/m0/s1

1 reference

Astilbin (English)

6 October 2016

2 references

Astilbin (English)

6 October 2016

ChEBI release 2020-09-01

2 references

astilbin (English)

6 October 2016

https://commonchemistry.cas.org/detail?cas_rn=29838-67-3

8 April 2021

1 reference

Astilbin (English)

6 October 2016

2 references

English

Astilbin (English)

6 October 2016

InChIKey

Reaxys registry number

100564

1 reference

astilbin (English)

6 October 2016

mapping relation type

2 references

English

astilbin (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H22O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-26,28-29H,1H3/t7-,15-,17+,18+,19+,20-,21-/m0/s1

1 reference

splash10-0udi-0941200000-7752c995c6f2cbdea0b4

ASTILBIN (English)

6 October 2016

1 reference

0 references

splash10-0abi-4973000000-4834cf38b559208d69ef

0 references

DSSTox substance ID

DTXSID501019948

1 reference

InChIKey

EC number

694-695-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.222.924

27 December 2018

ECHA Substance Infocard ID

(2S,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one (English)

quotation

CAS no.: 29838-67-3 (English)

100.222.924

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.222.924

27 December 2018

Human Metabolome Database ID

(2S,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one (English)

quotation

CAS no.: 29838-67-3 (English)

HMDB0033850

2 references

InChIKey