Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@@H]1[C@@H]2C[C@@H]3N(CC[C@@]45C6=CC7=C(C=C6O[C@@]34N1C1=CC=CC=C51)[C@@]13CCN4C\C(=C\C)[C@@H](C[C@H]4[C@@H]1N7C)[C@H]3C(=O)OC)C\C2=C\C

InChIKey

InChIKey=DQCQZSHDSKTQMX-LQAAYDTDSA-N

Formula

C41H46N4O5

Mass

674.842

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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 - Carbazole - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - Quinolizidine - Coumaran - Indole or derivatives - Piperidinecarboxylic acid - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Aralkylamine - Benzenoid - Piperidine - Dicarboxylic acid or derivatives - Methyl ester - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organic oxygen 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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