Structure Information
Structure

Compound Identification

SMILES

[Na+].CCOC(=O)C(N=NC1=C(C=C(C=C1)C1=NC2=C(S1)C=C(C=C2)C1=NC2=C(S1)C=C(C)C=C2)S([O-])(=O)=O)C(C)=O

InChIKey

InChIKey=CLUOBTYWBYLXLV-UHFFFAOYSA-M

Formula

C27H21N4NaO6S3

Mass

616.66

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Alpha amino acid esters

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Alpha-amino acid ester - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1,3-benzothiazole - 1-sulfo,2-unsubstituted aromatic compound - Beta-keto acid - Fatty acid ester - Monocyclic benzene moiety - Keto acid - Fatty acyl - 1,3-dicarbonyl compound - Benzenoid - Azole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Thiazole - Azo compound - Carboxylic acid ester - Ketone - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Organic alkali metal salt - Monocarboxylic acid or derivatives - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Hydrocarbon derivative - Organic sodium salt - Organic oxygen compound - Organic salt - Organic zwitterion - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

External Descriptors

Not available

Previous Back Next