CHEBI:66303 - rhinacanthin C

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ChEBI Name rhinacanthin C
ChEBI ID CHEBI:66303
Definition A naphthoquinone isolated from Rhinacanthus nasutus and has been shown to exhibit antiviral activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C25H30O5
Net Charge 0
Average Mass 410.50270
Monoisotopic Mass 410.20932
InChI InChI=1S/C25H30O5/c1-6-16(2)10-9-11-17(3)24(29)30-15-25(4,5)14-20-21(26)18-12-7-8-13-19(18)22(27)23(20)28/h6-8,11-13,28H,9-10,14-15H2,1-5H3/b16-6+,17-11+
InChIKey HBWJZSWEQJLURT-QIGLBIQCSA-N
SMILES C\C=C(/C)CC\C=C(/C)C(=O)OCC(C)(C)CC1=C(O)C(=O)c2ccccc2C1=O
Metabolite of Species Details
Rhinacanthus nasutus (NCBI:txid537489) See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antiviral agent
A substance that destroys or inhibits replication of viruses.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing rhinacanthin C (CHEBI:66303) has role antineoplastic agent (CHEBI:35610)
rhinacanthin C (CHEBI:66303) has role antiviral agent (CHEBI:22587)
rhinacanthin C (CHEBI:66303) has role metabolite (CHEBI:25212)
rhinacanthin C (CHEBI:66303) is a carboxylic ester (CHEBI:33308)
rhinacanthin C (CHEBI:66303) is a enoate ester (CHEBI:51702)
rhinacanthin C (CHEBI:66303) is a enol (CHEBI:33823)
rhinacanthin C (CHEBI:66303) is a hydroxy-1,4-naphthoquinone (CHEBI:132157)
IUPAC Name
3-(3-hydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-2,2-dimethylpropyl (2E,6E)-2,6-dimethylocta-2,6-dienoate
Registry Number Type Source
7391477 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
15256742 PubMed citation Europe PMC
19303271 PubMed citation Europe PMC
19403288 PubMed citation Europe PMC
23025179 PubMed citation Europe PMC
23393336 PubMed citation Europe PMC
8792629 PubMed citation Europe PMC
Last Modified
09 June 2016