Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1C2CC3C4NC5=CC=CC=C5C4CCN3CC2C(C)OC1C1C2C(CN3C=CC4=C5C=CC=CC5=NC4=C13)C(C)OC=C2C(=O)OC

InChIKey

InChIKey=DZCKWORLHZZPNE-UHFFFAOYSA-N

Formula

C42H46N4O6

Mass

702.852

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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

Ajmalicine-skeleton - 18-oxayohimban - Corynanthean skeleton - Yohimban skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - Quinolizidine - Indole - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Aralkylamine - Benzenoid - Dicarboxylic acid or derivatives - Oxane - Piperidine - Pyridine - Methyl ester - Vinylogous ester - Heteroaromatic compound - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Pyrrole - Carboxylic acid ester - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Dialkyl ether - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Secondary amine - Azacycle - Oxacycle - Amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organic nitrogen 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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