Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1OC(=O)C[C@H]2CC(=O)N(CCC3CN(C(=O)C4=CC=CC=C4)C4=CC=CC=C34)C[C@H]12

InChIKey

InChIKey=DZZHRXBAOAEVDI-XRSKCJJXSA-N

Formula

C26H28N2O4

Mass

432.52

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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

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