Structure Information
Structure

Compound Identification

SMILES

C[C@H]1OC[C@H]2[C@@H]3N(C(=O)CO)C4=CC=CC=C4C33CCN4C[C@@H]1[C@@H]2C[C@@H]34

InChIKey

InChIKey=OFRNYTYFWBPXRC-LDPZEHPRSA-N

Formula

C21H26N2O3

Mass

354.45

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Strychnos alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Strychnos alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Strychnan skeleton - Akuammicine-skeleton - Yohimban skeleton - Yohimbine alkaloid - Stemmadenine-skeleton - Carbazole - Indole or derivatives - Indolizidine - Aralkylamine - Oxane - Piperidine - Benzenoid - N-alkylpyrrolidine - Tertiary carboxylic acid amide - Pyrrolidine - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Carboxamide group - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Amine - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

External Descriptors

Not available

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