Structure Information
Structure

Compound Identification

SMILES

CC[C@]12CC(C(=O)OC)=C3NC4=CC5=C(C=C4[C@@]33CCN(CC=C1)[C@H]23)[C@H]1[C@@H](O5)[C@H](O)[C@]2(CC)CC(C(=O)OC)=C3NC4=C(OC)C(OC)=C(O)C=C4[C@@]33CCN1[C@H]23

InChIKey

InChIKey=XVLKCTCGGIJHCK-GXLFRJOSSA-N

Formula

C44H50N4O9

Mass

778.903

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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 - Plumeran-type alkaloid - Carbazole - Coumaran - Indole or derivatives - Dihydroindole - Indolizidine - Anisole - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Secondary aliphatic/aromatic amine - Dicarboxylic acid or derivatives - Benzenoid - Piperidine - N-alkylpyrrolidine - Enoate ester - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Vinylogous amide - Amino acid or derivatives - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Secondary amine - Carboxylic acid derivative - Enamine - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - 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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