Structure Information
Structure

Compound Identification

SMILES

CC1OC(=O)CC2CC(=O)N(CCC3CN(C(=O)OCC4=CC=CC=C4)C4=CC=CC=C34)CC12

InChIKey

InChIKey=AMOLYMXAGMCJFB-UHFFFAOYSA-N

Formula

C27H30N2O5

Mass

462.546

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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 - Indolecarboxylic acid - Indolecarboxylic acid derivative - Benzyloxycarbonyl - Indole or derivatives - Delta-lactam - Delta valerolactone - Delta_valerolactone - Piperidinone - Piperidine - Oxane - Benzenoid - Monocyclic benzene moiety - Carbamic acid ester - Tertiary carboxylic acid amide - Lactone - Lactam - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen 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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