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Structure Information
Structure

Compound Identification

SMILES

CCC12CCCN3CCC4(C(CC1)N(OC)C1=C(C=CC(O)=C41)C1CC4(CC)CCCN5CCC6=C(C45)N1C1=CC=CC=C61)C23

InChIKey

InChIKey=BJURQQRYZAQHSP-UHFFFAOYSA-N

Formula

C39H50N4O2

Mass

606.855

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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 - Pyridoindole - Beta-carboline - Carbazole - Naphthyridine - 3-alkylindole - Quinolidine - Indole - Indole or derivatives - Indolizidine - 1-hydroxylamino, 4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - N-alkylpyrrolidine - Benzenoid - Piperidine - Heteroaromatic compound - Pyrrolidine - Pyrrole - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - N-organohydroxylamine - Azacycle - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen 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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