conferol A (CHEBI:65653)

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ChEBI Name	conferol A

ChEBI ID	CHEBI:65653

Definition	A member of the class of isoflavans that is isoflavan with hydroxy substituents at positions 4, 7 and 4' and a methoxy group at position 2 (the 3R,4S stereoisomer). It is isolated from Caragana conferta and exhibits significant anti-inflammatory activity in the respiratory burst assay.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C16H16O5

Net Charge

Average Mass

288.29520

Monoisotopic Mass

288.09977

InChI

InChI=1S/C16H16O5/c1-20-14-6-9(17)2-4-11(14)13-8-21-15-7-10(18)3-5-12(15)16(13)19/h2-7,13,16-19H,8H2,1H3/t13-,16+/m0/s1

InChIKey

ILYFLNKVHSPXAN-XJKSGUPXSA-N

SMILES

[H][C@]1(COc2cc(O)ccc2[C@H]1O)c1ccc(O)cc1OC

Metabolite of Species	Details
caragana conferta (NCBI:txid626677)	Found in whole plant (BTO:0001461). See: PubMed

Roles Classification
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):	anti-inflammatory agent Any compound that has anti-inflammatory effects.

ChEBI Ontology
Outgoing	conferol A (CHEBI:65653) has role anti-inflammatory agent (CHEBI:67079) conferol A (CHEBI:65653) has role metabolite (CHEBI:25212) conferol A (CHEBI:65653) is a hydroxyisoflavans (CHEBI:76250) conferol A (CHEBI:65653) is a monomethoxybenzene (CHEBI:25235) conferol A (CHEBI:65653) is a secondary alcohol (CHEBI:35681)

IUPAC Name

(3R,4S)-3-(4-hydroxy-2-methoxyphenyl)-3,4-dihydro-2H-chromene-4,7-diol

Registry Number	Type	Source
19728201	Reaxys Registry Number	Reaxys

Citation	Type	Source
19336940	PubMed citation	Europe PMC

Last Modified

13 November 2013