CHEBI:9061 - scullcapflavone II

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ChEBI Name scullcapflavone II
ChEBI ID CHEBI:9061
Definition A tetramethoxyflavone that is flavone substituted by methoxy groups at positions 6, 7, 8 and 6' and hydroxy groups at positons 5 and 2' respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C19H18O8
Net Charge 0
Average Mass 374.34140
Monoisotopic Mass 374.10017
InChI InChI=1S/C19H18O8/c1-23-11-7-5-6-9(20)13(11)12-8-10(21)14-15(22)17(24-2)19(26-4)18(25-3)16(14)27-12/h5-8,20,22H,1-4H3
InChIKey GMQFOKBGMKVUQZ-UHFFFAOYSA-N
SMILES COc1cccc(O)c1-c1cc(=O)c2c(O)c(OC)c(OC)c(OC)c2o1
Metabolite of Species Details
Scutellaria baicalensis (NCBI:txid65409) See: PubMed
Roles Classification
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.
EC 1.6.5.2 [NAD(P)H dehydrogenase (quinone)] inhibitor
An EC 1.6.5.* (oxidoreductase acting on NADH or NADPH with a quinone or similar as acceptor) inhibitor that interferes with the action of NAD(P)H dehydrogenase (quinone), EC 1.6.5.2.
Application(s): anti-asthmatic drug
A drug used to treat asthma.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing scullcapflavone II (CHEBI:9061) has functional parent flavone (CHEBI:42491)
scullcapflavone II (CHEBI:9061) has role anti-asthmatic drug (CHEBI:49167)
scullcapflavone II (CHEBI:9061) has role EC 1.6.5.2 [NAD(P)H dehydrogenase (quinone)] inhibitor (CHEBI:50390)
scullcapflavone II (CHEBI:9061) has role plant metabolite (CHEBI:76924)
scullcapflavone II (CHEBI:9061) is a dihydroxyflavone (CHEBI:38686)
scullcapflavone II (CHEBI:9061) is a tetramethoxyflavone (CHEBI:76875)
IUPAC Name
5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one
Synonyms Sources
5,2'-dihydroxy-6,7,8,6'-tetramethoxyflavone ChEBI
5-hydroxy-2-(2-hydroxy-6-methoxy-phenyl)-6,7,8-trimethoxy-chromen-4-one ChEBI
neobaicalein KNApSAcK
skullcapflavone II LIPID MAPS
Manual Xrefs Databases
C00001099 KNApSAcK
C10183 KEGG COMPOUND
LMPK12111423 LIPID MAPS
View more database links
Registry Numbers Types Sources
3634558 Reaxys Registry Number Reaxys
55084-08-7 CAS Registry Number KEGG COMPOUND
55084-08-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
22314230 PubMed citation Europe PMC
25546119 PubMed citation Europe PMC
28886581 PubMed citation Europe PMC
31167359 PubMed citation Europe PMC
35398391 PubMed citation Europe PMC
36605189 PubMed citation Europe PMC
36697978 PubMed citation Europe PMC
36825003 PubMed citation Europe PMC
36865041 PubMed citation Europe PMC
37120983 PubMed citation Europe PMC
Last Modified
15 February 2024