Structure Information
Structure

Compound Identification

SMILES

Cl.CCOC(=O)NNC(=O)C1=CO[C@@H](C)[C@@H]2CN3CCC4=C(NC5=CC=CC=C45)[C@@H]3C[C@H]12

InChIKey

InChIKey=JOSDCESANLYFDL-JXOCOREXSA-N

Formula

C23H29ClN4O4

Mass

460.96

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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

18-oxayohimban - Corynanthean skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Hydrazinecarboxylic acid ester - Piperidine - Benzenoid - Heteroaromatic compound - Pyrrole - Vinylogous ester - Amino acid or derivatives - Carboxylic acid hydrazide - Tertiary amine - Tertiary aliphatic amine - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Carbonyl group - Hydrochloride - Organic nitrogen 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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