Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1C[C@H]2C[C@@]3(C1N(CCC1=C3NC3=CC([C@@H]4C[C@H]5C([C@H](CC6=C4NC4=CC=CC=C64)N(C)C\C5=C\C)C(=O)OC)=C(OC)C=C13)C2O)C(=O)OC

InChIKey

InChIKey=AGHLKWDCEVMWJG-UVHYDIRRSA-N

Formula

C43H52N4O6

Mass

720.911

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Ibogan-type alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Ibogan-type alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Ibogan skeleton - Vobasan skeleton - Catharanthine skeleton - Pyrroloazepine - 3-alkylindole - Indole - Indole or derivatives - Piperidinecarboxylic acid - Anisole - Phenol ether - Aralkylamine - Azepine - Alkyl aryl ether - Dicarboxylic acid or derivatives - Benzenoid - Piperidine - Methyl ester - Heteroaromatic compound - Pyrrole - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Hemiaminal - Carboxylic acid ester - Organoheterocyclic compound - Alkanolamine - Carboxylic acid derivative - Azacycle - Ether - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond.

External Descriptors

Not available

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