Structure Information
Structure

Compound Identification

SMILES

CCCCCC(=O)C1=C(OC)C=C2NC3=C(CCN4C[C@H]5C[C@@H](OC(=O)C6=CC(OC)=C(OC)C(OC)=C6)[C@H](OC)[C@H]([C@H]5C[C@H]34)C(=O)OC)C2=C1

InChIKey

InChIKey=SWPYDVACAWGCBQ-TWCOVTTNSA-N

Formula

C39H50N2O10

Mass

706.833

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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 - Beta-carboline - Pyridoindole - Gallic acid or derivatives - P-methoxybenzoic acid or derivatives - Butyrophenone - M-methoxybenzoic acid or derivatives - 3-alkylindole - Benzoate ester - Indole - Indole or derivatives - Benzoic acid or derivatives - Aryl ketone - Phenol ether - Phenoxy compound - Methoxybenzene - Benzoyl - Aryl alkyl ketone - Anisole - Aralkylamine - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Piperidine - Methyl ester - Pyrrole - Heteroaromatic compound - Tertiary amine - Tertiary aliphatic amine - Ketone - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Ether - Dialkyl ether - Organooxygen compound - Amine - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - 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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