Structure Information
Structure

Compound Identification

SMILES

CCC12CCC[N+]3(CC[C@]4(O)C5=C(CC6=C(C5)C(=O)C57CCN8C\C(=C\C)C9C[C@H]8[C@@]5(O6)N([C@@H]9C(=O)OC)C5=CC=CC=C75)NC34CC1)C2

InChIKey

InChIKey=PYKJXZODYXAERR-YRXHJFLYSA-N

Formula

C40H49N4O5

Mass

665.854

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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 - Azaspirodecane - Naphthyridine - Quinolizidine - Indole or derivatives - Indolizidine - Piperidinecarboxylic acid - Dialkylarylamine - Dihydropyranone - Aralkylamine - N-alkylpyrrolidine - Benzenoid - Piperidine - Methyl ester - Tertiary alcohol - Vinylogous ester - Quaternary ammonium salt - Pyrroline - Pyrrolidine - Tetraalkylammonium salt - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxylic acid ester - Ketone - Organoheterocyclic compound - Carboxylic acid derivative - Enamine - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxide - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organic cation - 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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