D-arabinitol (Q1880471)

Gene Ontology release 2019-11-16

D-arabitol catabolic process

subject has role

reactant

1 reference

Gene Ontology release 2019-11-16

D-arabitol metabolic process

subject has role

participant

1 reference

Gene Ontology release 2019-11-16

D-arabinitol dehydrogenase, D-ribulose forming (NADP+) activity

1 reference

D-arabinitol 2-dehydrogenase activity

1 reference

D-arabinitol 4-dehydrogenase activity

1 reference

D-arabinitol dehydrogenase, D-xylulose forming (NADP+) activity

1 reference

chemical structure

Arabitol.png
483 × 222; 4 KB

0 references

mass

152.068473 dalton

1 reference

D-Arabinitol (English)

5 October 2016

2 references

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₅H₁₂O₅

1 reference

D-Arabinitol (English)

5 October 2016

canonical SMILES

C(C(C(C(CO)O)O)O)O

1 reference

D-Arabinitol (English)

5 October 2016

isomeric SMILES

C([C@H](C([C@@H](CO)O)O)O)O

1 reference

D-Arabinitol (English)

5 October 2016

melting point

102.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

0

0

0

no value

1 reference

imported from Wikimedia project

1 reference

Water-soluble constituents of coriander

Euphorbia plumerioides

1 reference

Ent-14[S],16β,17-trihydroxyatisan-3-one and further constituents from Euphorbia fidjiana

Pisolithus arhizus

1 reference

The Structure and Absolute Stereochemistry of Pisosterol, the Principal Triterpenoid From Fruitbodies of the Fungus Pisolithus tinctorius

Pisolithus tinctorius

1 reference

The Structure and Absolute Stereochemistry of Pisosterol, the Principal Triterpenoid From Fruitbodies of the Fungus Pisolithus tinctorius

Ramalina fraxinea

1 reference

Chemical composition of the Ramalina fraxinea (L.) Ach. thallus

Stereocaulon ramulosum

1 reference

Isolation and identification of a linear (1→3)-linked β-d-glucan and other carbohydrate components of the lichen Stereocaulon ramulosum (SW.) Räusch

Diploicia canescens canescens

1 reference

Cytotoxic constituents of the lichen Diploicia canescens

Helicobasidium mompa

1 reference

Biochemistry of Filamentous Fungi. XIII. Metabolites ofHelicobasidium mompaTanaka

Salacia chinensis

1 reference

Salaprionol and Ponkoranol with Thiosugar Sulfonium Sulfate Structure from Salacia prinoides and a-Glucosidase Inhibitory Activity of Ponkoranol and Kotalanol Desulfate

Lethariella canariensis

1 reference

Canarion, ein neues naphthochinon aus Usnea canariensis

Arabidopsis thaliana

1 reference

Polyamine oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance.

tomato

1 reference

Metabolite content of harvested Micro-Tom tomato (Solanum lycopersicum L.) fruit is altered by chilling and protective heat-shock treatments as shown by GC–MS metabolic profiling

Ascochyta medicaginicola

1 reference

Time-course metabolic profiling in alfalfa leaves under Phoma medicaginis infection

Commons category

Arabitol

0 references

Identifiers

InChI

InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1

1 reference

D-Arabinitol (English)

5 October 2016

2 references

D-Arabinitol (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

488-82-4

1 reference

Global Substance Registration System

ARABINITOL, D- (English)

5 October 2016

1 reference

D-(+)-arabitol (English)

5 October 2016

2 references

D-Arabinitol (English)

5 October 2016

Reaxys registry number

1720520

1 reference

D-arabinitol (English)

5 October 2016

ChEBI ID

18333

mapping relation type

2 references

D-arabinitol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1

1 reference

MSBNK-Osaka_Univ-OUF00160

CHEMBL3186162 (English)

5 October 2016

1 reference

MassBank accession ID

0 references

MSBNK-GL_Sciences_Inc-GLS00172

0 references

SPLASH

splash10-0gba-0940000000-fd0f8e8fa319acbbf301

0 references

splash10-001r-3900000000-0c92d36e25a8849eca4e

0 references

splash10-00kf-0900000000-33c5242d2c263cf44ca9

0 references

splash10-03dj-0900000000-fa7230a4236cfe11c1f7

0 references

splash10-03di-3900000000-747d8f3e17f6f39e7254

0 references

splash10-0006-9000000000-356f6fde9f334c9d9284

0 references

splash10-0udi-0900000000-079c39d21ec576abbdfd

0 references

splash10-0gba-0941000000-9b75ceaa8f86d2a15e6c

0 references

NMRShiftDB structure ID

70128855

reason for deprecated rank

cannot be confirmed by other sources

0 references

DSSTox substance ID

DTXSID4045979

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

ARABINITOL, D- (English)

ECHA Substance Infocard ID

5 October 2016

100.006.988

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.988

27 December 2018

Human Metabolome Database ID

D-arabinitol (English)

quotation

CAS no.: 488-82-4 (English)

HMDB0000568

2 references

based on heuristic

inferred from InChIKey

1 reference

D-arabinitol (English)

5 October 2016

C00052193

2 references

based on heuristic

inferred from InChIKey

2 references

Global Substance Registration System

ARABINITOL, D- (English)

5 October 2016

YFV05Y57M9

1 reference