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Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12CCCN3CCC4=C([C@H]13)N([C@H](C2)C1=CC2=C(N[C@]35[C@H](C)[C@@]6(C[C@H]3C(=O)OC)C=CCN3CC[C@]25[C@H]63)C=C1)C1=CC=CC=C41

InChIKey

InChIKey=MZITZBZTMCXZQS-FVNDCLGZSA-N

Formula

C40H46N4O2

Mass

614.834

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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 - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - 2,3-cyclopentanoindoline - Aromatic monoterpenoid - Norbornane monoterpenoid - Monoterpenoid - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Dihydroindole - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyrrolidine - Pyrrole - Methyl ester - Heteroaromatic compound - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Secondary amine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Organooxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Organic oxide - 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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