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Structure Information
Structure

Compound Identification

SMILES

CC[C@@H]1C[C@@H]2CC(O)(N3C4=CC=CC=C4C4=C3[C@@H]2N(CC4)C1=O)C(=O)OC

InChIKey

InChIKey=HQBVMWYFIZVXBO-VLRKXRPRSA-N

Formula

C21H24N2O4

Mass

368.433

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Tacaman alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Tacaman alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Tacaman alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Delta-lactam - Piperidinone - Piperidine - Benzenoid - Pyrrole - Tertiary carboxylic acid amide - Methyl ester - Heteroaromatic compound - Carboxamide group - Carboxylic acid ester - Lactam - Monocarboxylic acid or derivatives - Alkanolamine - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as tacaman alkaloids. These are alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17.

External Descriptors

Not available

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