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Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=NYLMYCHXIHMDRS-YAFGAGFVSA-L

Formula

C21H26N2O7S

Mass

450.51

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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 - Pyridoindole - Naphthyridine - 3-alkylindole - Alpha-amino acid or derivatives - Indole - Indole or derivatives - Aralkylamine - Organic sulfate salt - Benzenoid - Piperidine - Heteroaromatic compound - Organic sulfuric acid or derivatives - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Alkanolamine - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Amine - Organic anion - 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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