Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=C2NC3=CC=CC=C3C22CCN3CC4(CC5CC67CCOC6CCN6CCC8(C76)C6=C(N(C4)C58O)C(OC)=CC=C6)C4OCCC4(C1)C23

InChIKey

InChIKey=IIMPGJMHQMBXKL-UHFFFAOYSA-N

Formula

C43H50N4O6

Mass

718.895

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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 - Cyclic alcohol - Vinylogous amide - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Tetrahydrofuran - Methyl ester - Enoate ester - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Secondary amine - Carboxylic acid derivative - Alkanolamine - Dialkyl ether - Enamine - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - 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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