Structure Information
Structure

Compound Identification

SMILES

COC1C(CC2CN3CCC4=C(NC5=CC(OC)=CC=C45)C3CC2C1C(=O)OC)OC(O)C(=CC1=CC(OC)=C(OC)C(OC)=C1)C(O)=O

InChIKey

InChIKey=WGFSDYQYZAACNU-UHFFFAOYSA-N

Formula

C36H44N2O11

Mass

680.751

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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 - Corynanthean skeleton - Yohimbine alkaloid - Pyridoindole - Beta-carboline - Cinnamic acid - Cinnamic acid or derivatives - Coumaric acid or derivatives - 3-alkylindole - Cinnamyl alcohol - Indole or derivatives - Indole - Phenol ether - Anisole - Phenoxy compound - Methoxybenzene - Beta-hydroxy acid - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydroxy acid - Benzenoid - Piperidine - Pyrrole - Methyl ester - Heteroaromatic compound - Tertiary amine - Amino acid or derivatives - Hemiacetal - Tertiary aliphatic amine - Amino acid - Carboxylic acid ester - Ether - Dialkyl ether - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organooxygen compound - Amine - Organic oxygen 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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