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Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=HUJHMNHVYIYOMD-NJSLBKSFSA-N

Formula

C21H24N2O2

Mass

336.435

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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 - Naphthyridine - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Enoate ester - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Amine - Organonitrogen 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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