Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OP(O)(O)=O)[C@H](O)[C@@H](O)[C@@H]1O.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)C(=C2)C(=O)OC

InChIKey

InChIKey=IVYZKAJKXRPDKP-CHQOHFEQSA-N

Formula

C27H37N2O11P

Mass

596.57

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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 - Beta-carboline - Pyridoindole - Hexose monosaccharide - Alpha-amino acid or derivatives - 3-alkylindole - Monosaccharide phosphate - Naphthyridine - Indole - Indole or derivatives - Aralkylamine - Monoalkyl phosphate - Organic phosphoric acid derivative - Piperidine - Alkyl phosphate - Oxane - Phosphoric acid ester - Benzenoid - Monosaccharide - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Pyrrole - Tertiary aliphatic amine - Amino acid or derivatives - Secondary alcohol - Tertiary amine - Carboxylic acid ester - Polyol - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Amine - Organonitrogen compound - Primary alcohol - 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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