Structure Information
Structure

Compound Identification

SMILES

[H][C@@](C)(OC(=O)C=C(C)C)[C@]12CCCN3CC[C@]4(C(NC5=C4C=CC(OC)=C5)=C(C1)C(=O)OC)[C@]23[H]

InChIKey

InChIKey=YTBDSGGHFWAARB-NPFRWRFASA-N

Formula

C27H34N2O5

Mass

466.578

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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 - Indole or derivatives - Dihydroindole - Indolizidine - Anisole - Alkyl aryl ether - Fatty acid ester - Aralkylamine - Secondary aliphatic/aromatic amine - Dicarboxylic acid or derivatives - Fatty acyl - Piperidine - Benzenoid - N-alkylpyrrolidine - Alpha,beta-unsaturated carboxylic ester - Pyrrolidine - Vinylogous amide - Enoate ester - Methyl ester - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Carboxylic acid ester - Secondary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Enamine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Amine - Organonitrogen compound - Organooxygen 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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