Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](C[C@@H]2CN3CC[C@]4(O[C@@H]3CC2[C@@H]1C(=O)OC)C(=O)NC1=C4C=CC(OC)=C1)OC(=O)C1=CC(OC)=C(OC)C(OC)=C1

InChIKey

InChIKey=LCGSFPHZIMPWFS-GJPFIKHHSA-N

Formula

C33H40N2O11

Mass

640.686

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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

Yohimban skeleton - Yohimbine alkaloid - Gallic acid or derivatives - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Benzoate ester - Dihydroindole - Indole or derivatives - Benzoic acid or derivatives - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Benzoyl - Alkyl aryl ether - Piperidine - Monocyclic benzene moiety - Oxazinane - 1,3-oxazinane - Benzenoid - Methyl ester - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Hemiaminal - Lactam - Ether - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Monocarboxylic acid or derivatives - Amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen 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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