Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1CC23CCOC2C2(CC4CC56CCOC5CCN5CCC7(C65)C5=CC=C(OC)C=C5N(C2)C47O)CN2CCC4(C32)C2=C(NC14O)C=CC=C2

InChIKey

InChIKey=DVMSYPCIAVODIK-UHFFFAOYSA-N

Formula

C43H52N4O7

Mass

736.91

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Aspidospermatan-type alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Aspidospermatan-type alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Aspidosperma alkaloid - Carbazole - Azaspirodecane - Quinolidine - Indole or derivatives - Dihydroindole - Indolizidine - Anisole - Dialkylarylamine - Alkyl aryl ether - Aralkylamine - Secondary aliphatic/aromatic amine - Piperidine - Benzenoid - N-alkylpyrrolidine - Tetrahydrofuran - Methyl ester - Pyrrolidine - Cyclic alcohol - Tertiary amine - Carboxylic acid ester - Tertiary aliphatic amine - Amino acid or derivatives - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Alkanolamine - Secondary amine - Carboxylic acid derivative - Amine - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids.

External Descriptors

Not available

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