Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12CCCN3CC[C@@]4([C@@H](CC1)NC1=C(C=CC(O)=C41)C1C[C@@]4(CC)CCCN5CCC6=C([C@@H]45)N1C1=CC=CC=C61)[C@@H]23

InChIKey

InChIKey=HHCOPHVLECRPRE-CDAWUECISA-N

Formula

C38H48N4O

Mass

576.829

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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

Aromatic heteropolycyclic compounds

Substituents

Eburna alkaloid - Aspidosperma alkaloid - Plumeran-type alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - Naphthyridine - 3-alkylindole - Quinolidine - Indole - Indole or derivatives - Dihydroindole - Indolizidine - Secondary aliphatic/aromatic amine - Aralkylamine - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Piperidine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Pyrrole - Heteroaromatic compound - Tertiary amine - Tertiary aliphatic amine - Secondary amine - Azacycle - Organoheterocyclic compound - Organooxygen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen 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

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