CHEBI:28429 - (+)-dihydromyricetin

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ChEBI Name (+)-dihydromyricetin
ChEBI ID CHEBI:28429
Definition An optically active form of dihydromyricetin having (2R,3R)-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:21, CHEBI:18447
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Formula C15H12O8
Net Charge 0
Average Mass 320.25098
Monoisotopic Mass 320.053
InChI InChI=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
InChIKey KJXSIXMJHKAJOD-LSDHHAIUSA-N
SMILES O[C@@H]1[C@H](Oc2cc(O)cc(O)c2C1=O)c1cc(O)c(O)c(O)c1
Metabolite of Species Details
Ampelopsis cantoniensis (NCBI:txid345095) Found in root (BTO:0001188). See: PubMed
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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ChEBI Ontology
Outgoing (+)-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 (−)-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 Sources
(+)-Ampelopsin KEGG COMPOUND
(+)-Dihydromyricetin KEGG COMPOUND
(+)-Dihydromyricetin KEGG COMPOUND
(2R,3R)-2,3-dihydro-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one ChEBI
(2R,3R)-3,3',4',5,5',7-hexahydroxy-2,3-dihydroflavanonol ChEBI
(2R,3R)-3,5,7,3',4',5'-hexahydroxyflavanone ChEBI
Ampelopsin KEGG COMPOUND
Ampeloptin ChemIDplus
Dihydromyricetin KEGG COMPOUND
Manual Xrefs Databases
C00000938 KNApSAcK
C02906 KEGG COMPOUND
CPD-7087 MetaCyc
Dihydromyricetin Wikipedia
View more database links
Registry Numbers Types Sources
27200-12-0 CAS Registry Number KEGG COMPOUND
27200-12-0 CAS Registry Number ChemIDplus
4331256 Beilstein Registry Number Beilstein
5303758 Reaxys Registry Number Reaxys
5303758 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
12889119 PubMed citation Europe PMC
17059013 PubMed citation Europe PMC
22693649 PubMed citation Europe PMC
Last Modified
06 February 2018