Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=C2NC3=C(C=CC(OC)=C3)[C@@]22CCN3CCC[C@](C1)([C@@H](C)OC(=O)C1=CC(OC)=C(OC)C(OC)=C1)[C@H]23

InChIKey

InChIKey=LUYXSVXUFFVNQZ-DMSKZVPASA-N

Formula

C32H38N2O8

Mass

578.662

Export to:

JSON SDF CSV

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 - Gallic acid or derivatives - P-methoxybenzoic acid or derivatives - M-methoxybenzoic acid or derivatives - Benzoate ester - Indolizidine - Dihydroindole - Indole or derivatives - Benzoic acid or derivatives - Phenoxy compound - Methoxybenzene - Phenol ether - Benzoyl - Anisole - Aralkylamine - Secondary aliphatic/aromatic amine - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Piperidine - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Vinylogous amide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Secondary amine - Ether - Enamine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - 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

Previous Back Next