Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@@H]1[C@H]2C[C@@H]3N(CC[C@]45C6=CC=CC=C6N1[C@]34OC1=C5C=CC(C(O)=O)=C1O)C\C2=C\C

InChIKey

InChIKey=YNVANSDYAYJCOX-WPROBLGFSA-N

Formula

C27H26N2O6

Mass

474.513

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Pleiocarpaman alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pleiocarpaman alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pleiocarpaman skeleton - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Hydroxybenzoic acid - Naphthyridine - Quinolizidine - Salicylic acid or derivatives - Coumaran - Piperidinecarboxylic acid - Indole or derivatives - Dialkylarylamine - Aralkylamine - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Benzenoid - Piperidine - Vinylogous acid - Methyl ester - Amino acid - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organooxygen compound - Amine - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pleiocarpaman alkaloids. These are alkaloids with a structure that is based on the pleiocarpaman skeleton. These alkaloids arise from the cyclization of a corynantheine precursor via C-16 to N-1.

External Descriptors

Not available

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