Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1COC(C)C2C3N(CCC33C(=O)Nc4ccccc34)CCC12

InChIKey

InChIKey=VAKVMFAPWWZUCY-UHFFFAOYSA-N

Formula

C21H26N2O4

Mass

370.449

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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 - Methyl ester - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Amine - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxide - 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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