cassameridine (CHEBI:132894)

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ChEBI Name	cassameridine

ChEBI ID	CHEBI:132894

Definition	An oxoaporphine alkaloid that is 7H-dibenzo[de,g]quinolin-7-one which is substituted by methylenedioxy grups at the 1,2 and 9,10 positions. Compared with liriodenine, which lacks the 9,10-methylenedioxy group, cassameridine displays only moderate antifungal activity.

Stars	This entity has been manually annotated by the ChEBI Team.

Submitter	qingping liu

Supplier Information

Download	Molfile XML SDF

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Formula

C18H9NO5

Net Charge

Average Mass

319.268

Monoisotopic Mass

319.04807

InChI

InChI=1S/C18H9NO5/c20-17-10-5-12-11(21-6-22-12)4-9(10)15-14-8(1-2-19-16(14)17)3-13-18(15)24-7-23-13/h1-5H,6-7H2

InChIKey

ANNPRBPTCAXMQI-UHFFFAOYSA-N

SMILES

C=12C(C3=NC=CC4=CC5=C(C(C1C=C6C(=C2)OCO6)=C34)OCO5)=O

Metabolite of Species	Details
Cassytha filiformis (NCBI:txid121073)	See: Phytochemistry, 1997, 46, 181
Stephania tetrandra (NCBI:txid425106)	See: J. Nat. Prod.,1992, 55, 828

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. metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. (via alkaloid )

ChEBI Ontology
Outgoing	cassameridine (CHEBI:132894) has role plant metabolite (CHEBI:76924) cassameridine (CHEBI:132894) is a cyclic acetal (CHEBI:59770) cassameridine (CHEBI:132894) is a cyclic ketone (CHEBI:3992) cassameridine (CHEBI:132894) is a organic heterohexacyclic compound (CHEBI:51914) cassameridine (CHEBI:132894) is a organonitrogen heterocyclic compound (CHEBI:38101) cassameridine (CHEBI:132894) is a oxoaporphine alkaloid (CHEBI:132998)

IUPAC Name

8H-bis[1,3]benzodioxolo[6,5,4-de:5',6'-g]quinolin-8-one

Synonym	Source
cassameridin	KNApSAcK

Registry Number	Type	Source
1088882	Reaxys Registry Number	Reaxys

Citation	Type	Source
7420287	PubMed citation	Europe PMC

Last Modified

12 August 2016