Structure Information
Structure

Compound Identification

SMILES

CC[C@]12CCCN(C1)CCC1=C(CC2)NC2=CC3=C(C[C@]45CCN6C\C(=C\C)[C@@H]7C[C@H]6[C@@]4(O3)N([C@@H]7C(=O)OC)C3=CC=CC=C53)C=C12

InChIKey

InChIKey=FXNSZAOKKBWFLU-QUXVBKSJSA-N

Formula

C40H48N4O3

Mass

632.849

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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 - Quebrachamine skeleton - Isoflavan - Isoflavonoid - Indolo[3,2-1de][1,5]naphthyridine - Alpha-amino acid ester - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - 3-alkylindole - Benzopyran - 1-benzopyran - Naphthyridine - Chromane - Quinolizidine - Indole - Indole or derivatives - Piperidinecarboxylic acid - Dialkylarylamine - Aralkylamine - Benzenoid - Piperidine - Heteroaromatic compound - Methyl ester - Pyrrole - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid ester - Amino acid or derivatives - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic oxide - 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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