Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12CCCN3CCC4=C([C@H]13)N([C@H](C2)C1=C(OC)C=C2NC3=C([C@H](O)[C@]5(CC)C=CCN6CC[C@]3([C@H]56)C2=C1)C(=O)OC)C1=CC=CC=C41

InChIKey

InChIKey=ZTNSUFUGEHKDNP-OLHHKJETSA-N

Formula

C41H48N4O4

Mass

660.859

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