Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1[C@H](O)O[C@@H](C)[C@H]2CN3CC[C@@]4([C@@H]3C[C@H]12)C(=O)NC1=CC=CC=C41

InChIKey

InChIKey=BZEARLNMWSCOOH-GOCWHEHFSA-N

Formula

C21H26N2O5

Mass

386.448

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Yohimbine alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Yohimbine alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Yohimban skeleton - Yohimbine alkaloid - Indole or derivatives - Dihydroindole - Indolizidine - Beta-hydroxy acid - Aralkylamine - Hydroxy acid - Oxane - Piperidine - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Methyl ester - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Amino acid or derivatives - Lactam - Carboxamide group - Carboxylic acid ester - Hemiacetal - Oxacycle - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carbonyl group - Amine - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.

External Descriptors

Not available

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