CHEBI:68023 - cudraflavone C

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name cudraflavone C
ChEBI ID CHEBI:68023
Definition A tetrahydroxyflavone that is flavone substituted by hydroxy groups at positions 5, 7, 2' and 4' and prenyl groups at positions 3 and 6. Isolated from Morus nigra, it exhibits antibacterial and cytotoxic activities.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C25H26O6
Net Charge 0
Average Mass 422.47030
Monoisotopic Mass 422.17294
InChI InChI=1S/C25H26O6/c1-13(2)5-8-16-20(28)12-21-22(23(16)29)24(30)18(9-6-14(3)4)25(31-21)17-10-7-15(26)11-19(17)27/h5-7,10-12,26-29H,8-9H2,1-4H3
InChIKey MUUDYSFWQUSAOO-UHFFFAOYSA-N
SMILES CC(C)=CCc1c(O)cc2oc(-c3ccc(O)cc3O)c(CC=C(C)C)c(=O)c2c1O
Metabolite of Species Details
Morus nigra (NCBI:txid85232) Found in twig (BTO:0001411). Milled, air-dried twigs were percolated with 95% ethanol See: PubMed
Roles Classification
Biological Role(s): antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cudraflavone C (CHEBI:68023) has role antibacterial agent (CHEBI:33282)
cudraflavone C (CHEBI:68023) has role antineoplastic agent (CHEBI:35610)
cudraflavone C (CHEBI:68023) has role plant metabolite (CHEBI:76924)
cudraflavone C (CHEBI:68023) is a tetrahydroxyflavone (CHEBI:38684)
IUPAC Name
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one
Synonyms Sources
2',4',5,7-tetrahydroxy-3,6-bis(3-methyl-2-butenyl)flavone ChEBI
2-(2,4-dihydroxy-phenyl)-5,7-dihydroxy-3,6-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one ChEBI
mulberrin ChEBI
Manual Xref Database
LMPK12110902 LIPID MAPS
View more database links
Registry Numbers Types Sources
1334252 Reaxys Registry Number Reaxys
19275-47-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10821057 PubMed citation Europe PMC
12391560 PubMed citation Europe PMC
19686821 PubMed citation Europe PMC
20020453 PubMed citation Europe PMC
20628938 PubMed citation Europe PMC
21401118 PubMed citation Europe PMC
21941923 PubMed citation Europe PMC
22344915 PubMed citation Europe PMC
23835832 PubMed citation Europe PMC
Last Modified
01 October 2014