CHEBI:5837 - hypolaetin

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ChEBI Name hypolaetin
ChEBI ID CHEBI:5837
Definition A pentahydroxyflavone that consists of luteolin substituted by an additional hydroxy group at position 8.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H10O7
Net Charge 0
Average Mass 302.23570
Monoisotopic Mass 302.04265
InChI InChI=1S/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H
InChIKey ASOIXDIITRKTOX-UHFFFAOYSA-N
SMILES Oc1ccc(cc1O)-c1cc(=O)c2c(O)cc(O)c(O)c2o1
Metabolite of Species Details
Sideritis scardica (NCBI:txid155261) 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): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing hypolaetin (CHEBI:5837) has functional parent luteolin (CHEBI:15864)
hypolaetin (CHEBI:5837) has role antioxidant (CHEBI:22586)
hypolaetin (CHEBI:5837) has role plant metabolite (CHEBI:76924)
hypolaetin (CHEBI:5837) is a pentahydroxyflavone (CHEBI:25883)
Incoming theograndin II (CHEBI:66218) has functional parent hypolaetin (CHEBI:5837)
IUPAC Name
2-(3,4-dihydroxyphenyl)-5,7,8-trihydroxy-4H-chromen-4-one
Synonyms Sources
8-Hydroxyluteolin KEGG COMPOUND
Hypolaetin KEGG COMPOUND
Manual Xrefs Databases
C00001053 KNApSAcK
C10078 KEGG COMPOUND
LMPK12111397 LIPID MAPS
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Registry Numbers Types Sources
27696-41-9 CAS Registry Number KEGG COMPOUND
317464 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21111424 PubMed citation Europe PMC
23140681 PubMed citation Europe PMC
23147814 PubMed citation Europe PMC
24102372 PubMed citation Europe PMC
IND44438910 Agricola citation Europe PMC
Last Modified
16 October 2014