Structure Information
Structure

Compound Identification

SMILES

CSCCC(NC(=O)NC(CCSC)C(=O)OC1=CC=C(C=C1)[N+]([O-])=O)C(=O)OC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=UAMQNDYCCRCTJH-UHFFFAOYSA-N

Formula

C23H26N4O9S2

Mass

566.6

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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

Methionine and derivatives

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Methionine or derivatives - Alpha-amino acid ester - N-carbamoyl-alpha-amino acid - N-carbamoyl-alpha-amino acid or derivatives - Phenol ester - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Fatty acid ester - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Benzenoid - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Carbonic acid derivative - Urea - Thioether - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organic oxoazanium - Dialkylthioether - Organosulfur compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organic zwitterion - Organooxygen compound - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

External Descriptors

Not available

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