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CHEBI:28429 - (+)-dihydromyricetin

ChEBI IDCHEBI:28429
ChEBI Name(+)-dihydromyricetin
Stars
DefinitionAn optically active form of dihydromyricetin having (2R,3R)-configuration.
Secondary ChEBI IDsCHEBI:21, CHEBI:18447
Last Modified6 August 2019
DownloadsMolfile
FormulaC15H12O8
Net Charge0
Average Mass320.253
Monoisotopic Mass320.05322
SMILESO=C1c2c(O)cc(O)cc2O[C@H](c2cc(O)c(O)c(O)c2)[C@H]1O
InChIInChI=1S/C15H12O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,14-20,22H/t14-,15+/m0/s1
InChIKeyKJXSIXMJHKAJOD-LSDHHAIUSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Ampelopsis cantoniensis (ncbitaxon:345095) root (BTO:0001188) PubMed (17059013)
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
(+)-dihydromyricetin (CHEBI:28429) has role antineoplastic agent (CHEBI:35610)
(+)-dihydromyricetin (CHEBI:28429) has role antioxidant (CHEBI:22586)
(+)-dihydromyricetin (CHEBI:28429) has role metabolite (CHEBI:25212)
(+)-dihydromyricetin (CHEBI:28429) is a dihydromyricetin (CHEBI:28917)
(+)-dihydromyricetin (CHEBI:28429) is a secondary α-hydroxy ketone (CHEBI:2468)
(+)-dihydromyricetin (CHEBI:28429) is enantiomer of (−)-dihydromyricetin (CHEBI:48027)
Incoming Relation(s)
(−)-dihydromyricetin (CHEBI:48027) is enantiomer of (+)-dihydromyricetin (CHEBI:28429)
IUPAC Name 
(2R,3R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydro-4H-chromen-4-one
Synonyms  Source
(+)-DihydromyricetinKEGG COMPOUND
(+)-AmpelopsinKEGG COMPOUND
DihydromyricetinKEGG COMPOUND
AmpelopsinKEGG COMPOUND
AmpeloptinChemIDplus
(2R,3R)-3,5,7,3',4',5'-hexahydroxyflavanoneChEBI
UniProt Name  Source
(2R,3R)-dihydromyricetinUniProt
Manual XrefsDatabases
C02906KEGG COMPOUND
DihydromyricetinWikipedia
CPD-7087MetaCyc
C00000938KNApSAcK
Registry NumbersSources
Beilstein:4331256Beilstein
Reaxys:5303758Reaxys
CAS:27200-12-0KEGG COMPOUND
CAS:27200-12-0ChemIDplus
Citations