Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1O[C@@H](O)C(C#COO)[C@H]2C[C@@H]3N(CC[C@@]33C(=O)NC4=CC=CC=C34)C[C@H]12

InChIKey

InChIKey=WMCSSTWQESHHGU-GBAZDDPASA-N

Formula

C21H24N2O5

Mass

384.432

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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 - Aralkylamine - Oxane - Piperidine - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Carboxamide group - Hemiacetal - Lactam - Hydroperoxide - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Peroxol - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - 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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