Structure Information
Structure

Compound Identification

SMILES

OC(=O)C1=CC=CC=C1C(=O)C1=CC=C(O)C=C1.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)[C@](O)(C2)C(=O)OC

InChIKey

InChIKey=XKXCQCBOHAPNEP-YAFGAGFVSA-N

Formula

C35H36N2O7

Mass

596.68

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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

Not available

Substituents

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Benzophenone - Beta-carboline - Aryl-phenylketone - Diphenylmethane - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Benzoic acid - Benzoic acid or derivatives - Benzoyl - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Piperidine - Benzenoid - Monocyclic benzene moiety - Methyl ester - Pyrrole - Heteroaromatic compound - Amino acid or derivatives - Tertiary amine - Ketone - Tertiary aliphatic amine - Carboxylic acid ester - Carboxylic acid - Azacycle - Carboxylic acid derivative - Alkanolamine - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen 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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