Structure Information
Structure

Compound Identification

SMILES

[CH3].[O-]C(=O)CCC(=O)C([O-])=O.CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)[C@](O)(C2)C([O-])=O

InChIKey

InChIKey=SYJNAMJULTWRGG-UFUWJLJKSA-K

Formula

C26H30N2O8

Mass

498.534

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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 - Diazanaphthalene - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Gamma-keto acid - Short-chain keto acid - Aralkylamine - Alpha-keto acid - Dicarboxylic acid or derivatives - Keto acid - Piperidine - Benzenoid - Pyrrole - Heteroaromatic compound - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Ketone - Amino acid - Carboxylic acid salt - Azacycle - Organoheterocyclic compound - Alkanolamine - Carboxylic acid derivative - Carboxylic acid - Amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Hydrocarbon - Saturated hydrocarbon - 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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