Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)C(=O)C2.CC[C@@]12CCCN3CC[C@@]4([C@H]13)C(NC1=CC=CC=C41)=C(C2)C(=O)OC

InChIKey

InChIKey=DBCSLHKSNINCCQ-VNURXBPISA-N

Formula

C40H48N4O3

Mass

632.849

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Eburnan-type alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Eburnan-type alkaloids

Alternative Parents

Molecular Framework

Not available

Substituents

Eburna alkaloid - Aspidosperma alkaloid - Plumeran-type alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Dihydroindole - Indolizidine - Secondary aliphatic/aromatic amine - Aralkylamine - N-alkylpyrrolidine - Benzenoid - Piperidine - Vinylogous amide - Methyl ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Pyrrolidine - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Lactam - Secondary amine - Enamine - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic nitrogen compound - Amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.

External Descriptors

Not available

Previous Back Next