CHEBI:75902 - hispidulin

ChEBI IDCHEBI:75902
ChEBI Namehispidulin
Stars
DefinitionA monomethoxyflavone that is scutellarein methylated at position 6.
Secondary ChEBI IDCHEBI:5732
Last Modified26 February 2016
DownloadsMolfile
FormulaC16H12O6
Net Charge0
Average Mass300.266
Monoisotopic Mass300.06339
SMILESCOc1c(O)cc2oc(-c3ccc(O)cc3)cc(=O)c2c1O
InChIInChI=1S/C16H12O6/c1-21-16-11(19)7-13-14(15(16)20)10(18)6-12(22-13)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3
InChIKeyIHFBPDAQLQOCBX-UHFFFAOYSA-N
Wikipedia
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Roles:
apoptosis inducer  Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Applications:
anti-inflammatory agent  Any compound that has anti-inflammatory effects.
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
anticonvulsant  A drug used to prevent seizures or reduce their severity.
ChEBI Ontology
Outgoing Relation(s)
hispidulin (CHEBI:75902) has functional parent scutellarein (CHEBI:9062)
hispidulin (CHEBI:75902) has role anti-inflammatory agent (CHEBI:67079)
hispidulin (CHEBI:75902) has role anticonvulsant (CHEBI:35623)
hispidulin (CHEBI:75902) has role antineoplastic agent (CHEBI:35610)
hispidulin (CHEBI:75902) has role antioxidant (CHEBI:22586)
hispidulin (CHEBI:75902) has role apoptosis inducer (CHEBI:68495)
hispidulin (CHEBI:75902) has role plant metabolite (CHEBI:76924)
hispidulin (CHEBI:75902) is a monomethoxyflavone (CHEBI:25401)
hispidulin (CHEBI:75902) is a trihydroxyflavone (CHEBI:27116)
IUPAC Name 
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one
Synonyms  Source
HispidulinKEGG COMPOUND
Scutellarein 6-methyl etherKEGG COMPOUND
DinatinKEGG COMPOUND
NSC 122415ChemIDplus
4',5,7-Trihydroxy-6-methoxyflavoneChemIDplus
Manual XrefsDatabases
C10058KEGG COMPOUND
LMPK12111159LIPID MAPS
HispidulinWikipedia
C00001050KNApSAcK
Registry NumbersSources
Reaxys:1293933Reaxys
CAS:1447-88-7KEGG COMPOUND
CAS:1447-88-7ChemIDplus
Citations