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Structure Information
Structure

Compound Identification

SMILES

CC[C@]12C[C@@H](N3C4=CC=CC=C4C4=C3[C@H]1N(CC4)CC=C2)C1=CC2=C(N[C@]34[C@H](C)[C@@]5(C[C@H]3C(=O)OC)C=CC[N+]3([O-])CC[C@]24[C@H]53)C=C1

InChIKey

InChIKey=PZWIMIHBVUSBTP-FJMUIFANSA-N

Formula

C40H44N4O3

Mass

628.817

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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 - Monoterpenoid - Naphthyridine - Norbornane monoterpenoid - 3-alkylindole - Indole - Indole or derivatives - Dihydroindole - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - N-alkylpyrrolidine - Trialkyl amine oxide - Heteroaromatic compound - Pyrrole - Pyrrolidine - Methyl ester - Amino acid or derivatives - Carboxylic acid ester - Tertiary amine - Tertiary aliphatic amine - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - N-oxide - Secondary amine - Trisubstituted n-oxide - Organic salt - Amine - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - 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

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