CHEBI:75902 - hispidulin

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name hispidulin
ChEBI ID CHEBI:75902
Definition A monomethoxyflavone that is scutellarein methylated at position 6.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Secondary ChEBI IDs CHEBI:5732
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C16H12O6
Net Charge 0
Average Mass 300.26290
Monoisotopic Mass 300.06339
InChI InChI=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
InChIKey IHFBPDAQLQOCBX-UHFFFAOYSA-N
SMILES COc1c(O)cc2oc(cc(=O)c2c1O)-c1ccc(O)cc1
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): 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.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
anticonvulsant
A drug used to prevent seizures or reduce their severity.
antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 Sources
4',5,7-Trihydroxy-6-methoxyflavone ChemIDplus
Dinatin KEGG COMPOUND
Hispidulin KEGG COMPOUND
NSC 122415 ChemIDplus
Scutellarein 6-methyl ether KEGG COMPOUND
Manual Xrefs Databases
C00001050 KNApSAcK
C10058 KEGG COMPOUND
Hispidulin Wikipedia
LMPK12111159 LIPID MAPS
View more database links
Registry Numbers Types Sources
1293933 Reaxys Registry Number Reaxys
1447-88-7 CAS Registry Number KEGG COMPOUND
1447-88-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11585687 PubMed citation Europe PMC
20117183 PubMed citation Europe PMC
20698539 PubMed citation Europe PMC
20734985 PubMed citation Europe PMC
20738216 PubMed citation Europe PMC
21087351 PubMed citation Europe PMC
21162116 PubMed citation Europe PMC
21329950 PubMed citation Europe PMC
21552369 PubMed citation Europe PMC
22418930 PubMed citation Europe PMC
22674731 PubMed citation Europe PMC
22759588 PubMed citation Europe PMC
22978216 PubMed citation Europe PMC
23189738 PubMed citation Europe PMC
23791609 PubMed citation Europe PMC
24009700 PubMed citation Europe PMC
24068521 PubMed citation Europe PMC
Last Modified
26 February 2016