CHEBI:66297 - remangiflavanone A

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ChEBI Name remangiflavanone A
ChEBI ID CHEBI:66297
Definition A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5, 7 and 4' and a lavandulyl group at position 8. Isolated from Physena madagascariensis, it exhibits antibacterial activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C25H28O5
Net Charge 0
Average Mass 408.488
Monoisotopic Mass 408.19367
InChI InChI=1S/C25H28O5/c1-14(2)5-6-17(15(3)4)11-19-20(27)12-21(28)24-22(29)13-23(30-25(19)24)16-7-9-18(26)10-8-16/h7-10,12,17,23,26-28H,1,3,5-6,11,13H2,2,4H3/t17-,23+/m1/s1
InChIKey NPTHXJUVZWZDJB-HXOBKFHXSA-N
SMILES C1(C2=C(O[C@@H](C1)C3=CC=C(C=C3)O)C(=C(C=C2O)O)C[C@@H](CCC(=C)C)C(=C)C)=O
Metabolite of Species Details
Physena madagascariensis (NCBI:txid764924) Found in leaf (BTO:0000713). 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.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing remangiflavanone A (CHEBI:66297) has role antibacterial agent (CHEBI:33282)
remangiflavanone A (CHEBI:66297) has role metabolite (CHEBI:25212)
remangiflavanone A (CHEBI:66297) is a 4'-hydroxyflavanones (CHEBI:140331)
remangiflavanone A (CHEBI:66297) is a trihydroxyflavanone (CHEBI:38739)
IUPAC Name
(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-2,3-dihydro-4H-chromen-4-one
Synonyms Sources
(2S)-5,7,4'-trihydroxy-8-lavandulylflavanone ChEBI
(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R)-5-methyl-2-(1-methylethenyl)-5-hexen-1-yl]-2,3-dihydro-4H-1-benzopyran-4-one ChEBI
5,7,2',4'-tetrahydroxy-8-(2-isopropyl-5-methyl-5-hexenyl)flavanone LIPID MAPS
5,7,4'-trihydroxy-8-(2-isopropyl-5-methyl-5-hexenyl)flavanone LIPID MAPS
Manual Xref Database
LMPK12140299 LIPID MAPS
View more database links
Registry Number Type Source
8658227 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
10978202 PubMed citation Europe PMC
Last Modified
05 April 2018