CHEBI:61278 - scutellarin

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name scutellarin
Definition The glycosyloxyflavone which is the 7-O-glucuronide of scutellarein.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C21H18O12
Net Charge 0
Average Mass 462.36040
Monoisotopic Mass 462.07983
InChI InChI=1S/C21H18O12/c22-8-3-1-7(2-4-8)10-5-9(23)13-11(31-10)6-12(14(24)15(13)25)32-21-18(28)16(26)17(27)19(33-21)20(29)30/h1-6,16-19,21-22,24-28H,(H,29,30)/t16-,17-,18+,19-,21+/m0/s1
SMILES O[C@H]1[C@@H](O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O)Oc1cc2oc(cc(=O)c2c(O)c1O)-c1ccc(O)cc1
Roles Classification
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
proteasome inhibitor
A drug that blocks the action of proteasomes, cellular complexes that break down proteins.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing scutellarin (CHEBI:61278) has functional parent scutellarein (CHEBI:9062)
scutellarin (CHEBI:61278) has role antineoplastic agent (CHEBI:35610)
scutellarin (CHEBI:61278) has role proteasome inhibitor (CHEBI:52726)
scutellarin (CHEBI:61278) is a glucosiduronic acid (CHEBI:24302)
scutellarin (CHEBI:61278) is a glycosyloxyflavone (CHEBI:50018)
scutellarin (CHEBI:61278) is a monosaccharide derivative (CHEBI:63367)
scutellarin (CHEBI:61278) is a trihydroxyflavone (CHEBI:27116)
scutellarin (CHEBI:61278) is conjugate acid of scutellarin(1−) (CHEBI:61284)
Incoming scutellarin(1−) (CHEBI:61284) is conjugate base of scutellarin (CHEBI:61278)
5,6-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl β-D-glucopyranosiduronic acid
Synonyms Sources
Scutellarein 7-O-β-D-glucuronide ChEBI
Scutellarein-7-glucuronide ChemIDplus
Scutellarein-7-O-beta-D-glucuronide ChemIDplus
Scutellarein-7beta-D-glucuronide ChemIDplus
Scutellarein-7beta-D-glucuronoside ChemIDplus
Manual Xref Database
Scutellarin Wikipedia
View more database links
Registry Numbers Types Sources
27740-01-8 CAS Registry Number ChemIDplus
71779 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10724177 PubMed citation Europe PMC
22092277 PubMed citation Europe PMC
23147714 PubMed citation Europe PMC
23177255 PubMed citation Europe PMC
23192830 PubMed citation Europe PMC
Last Modified
05 February 2013