CHEBI:9992 - violanthin

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ChEBI Name violanthin
Definition A flavone C-glycoside that is flavone substituted by hydroxy groups at positions 5, 7 and 4', a β-D-glucopyranosyl residue at position 6 and a 6-deoxy-α-L-mannopyranosyl residue at position 8.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C27H30O14
Net Charge 0
Average Mass 578.51870
Monoisotopic Mass 578.16356
InChI InChI=1S/C27H30O14/c1-8-17(31)21(35)23(37)27(39-8)16-20(34)15(26-24(38)22(36)18(32)13(7-28)41-26)19(33)14-11(30)6-12(40-25(14)16)9-2-4-10(29)5-3-9/h2-6,8,13,17-18,21-24,26-29,31-38H,7H2,1H3/t8-,13+,17-,18+,21+,22-,23+,24+,26-,27-/m0/s1
SMILES C[C@@H]1O[C@H]([C@H](O)[C@H](O)[C@H]1O)c1c(O)c([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(O)c2c1oc(cc2=O)-c1ccc(O)cc1
Metabolite of Species Details
Viola tricolor (NCBI:txid214053) See: DOI
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 (acetylcholinesterase) inhibitor
An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC, which helps breaking down of acetylcholine into choline and acetic acid.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing violanthin (CHEBI:9992) has functional parent flavone (CHEBI:42491)
violanthin (CHEBI:9992) has role EC (acetylcholinesterase) inhibitor (CHEBI:38462)
violanthin (CHEBI:9992) has role plant metabolite (CHEBI:76924)
violanthin (CHEBI:9992) is a flavone C-glycoside (CHEBI:83280)
violanthin (CHEBI:9992) is a trihydroxyflavone (CHEBI:27116)
Manual Xrefs Databases
C00006230 KNApSAcK
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Registry Numbers Types Sources
40581-17-7 CAS Registry Number KEGG COMPOUND
6555620 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11320336 PubMed citation Europe PMC
25005067 PubMed citation Europe PMC
9548860 PubMed citation Europe PMC
Last Modified
16 October 2014