Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1CC2(C(C)O)C3OC3CN3CCC4(C23)C2=C(NC14O)C=CC=C2

InChIKey

InChIKey=JBRMEYYMJBQPKH-UHFFFAOYSA-N

Formula

C21H26N2O5

Mass

386.448

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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 - Quinolidine - Indolizidine - Dihydroindole - Indole or derivatives - Aralkylamine - Secondary aliphatic/aromatic amine - Para-oxazepine - Epoxypiperidine - Benzenoid - N-alkylpyrrolidine - Piperidine - Methyl ester - Pyrrolidine - 1,3-aminoalcohol - Cyclic alcohol - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Secondary amine - Alkanolamine - Carboxylic acid derivative - Dialkyl ether - Oxirane - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Amine - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Alcohol - 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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