CHEBI:142484 - (20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene

ChEBI IDCHEBI:142484
ChEBI Name(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene
Stars
ASCII Name(20S)-20-O-(beta-D-glucosyl)-3-hydroxydammarene
DefinitionA tetracyclic triterpenoid that is dammarenediol-II where the hydrogen of the hydroxy group at position 20 is replaced by a β-D-glucoside.
Last Modified5 November 2019
SubmitterKristian Axelsen
DownloadsMolfile
FormulaC36H62O7
Net Charge0
Average Mass606.885
Monoisotopic Mass606.44955
SMILES[H][C@]12CC[C@]3([H])[C@@]([H])([C@](C)(CCC=C(C)C)O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)CC[C@@]3(C)[C@]1(C)CC[C@@]1([H])C(C)(C)[C@@H](O)CC[C@]21C
InChIInChI=1S/C36H62O7/c1-21(2)10-9-16-36(8,43-31-30(41)29(40)28(39)24(20-37)42-31)23-13-18-34(6)22(23)11-12-26-33(5)17-15-27(38)32(3,4)25(33)14-19-35(26,34)7/h10,22-31,37-41H,9,11-20H2,1-8H3/t22-,23+,24-,25+,26-,27+,28-,29+,30-,31+,33+,34-,35-,36+/m1/s1
InChIKeyJQOUYGJYNQSCQP-UZTNOJNJSA-N
ChEBI Ontology
Outgoing Relation(s)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) has functional parent dammarenediol-II (CHEBI:62416)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) has parent hydride dammarane (CHEBI:36488)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) is a 3β-hydroxy steroid (CHEBI:36836)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) is a 3β-hydroxy-4,4-dimethylsteroid (CHEBI:143563)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) is a monosaccharide derivative (CHEBI:63367)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) is a tetracyclic triterpenoid (CHEBI:26893)
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammarene (CHEBI:142484) is a β-D-glucoside (CHEBI:22798)
IUPAC Name 
(3β)-3-hydroxydammar-24-en-20-yl β-D-glucopyranoside
Synonyms  Source
20-G-DMChEBI
3,20-dammarenediol 20-O-β-D-glucopyranosideChEBI
20-O-(β-D-glucopyranosyl)-DMChEBI
20-O-(β-D-glucopyranosyl)dammarenediol IIChEBI
(20S)-20-(β-D-glucopyranosyloxy)-dammara-24-ene-3β-olChEBI
UniProt Name  Source
(20S)-20-O-(β-D-glucosyl)-3-hydroxydammareneUniProt
Manual XrefsDatabases
CPD-21331MetaCyc
US2016115515Patent
Registry NumbersSources
Reaxys:29593714Reaxys
Citations