Structure Information
Structure

Compound Identification

SMILES

CSCC[C@H](NC(=O)C1=CC(=CC=C1)[N+]([O-])=O)C(=O)NC1=CC=C(F)C=C1

InChIKey

InChIKey=RBYDWQZMIMDWJZ-INIZCTEOSA-N

Formula

C18H18FN3O4S

Mass

391.42

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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 - N-acyl-alpha amino acid or derivatives - Hippuric acid or derivatives - Alpha-amino acid amide - Nitrobenzene - Benzamide - Anilide - Benzoic acid or derivatives - Nitroaromatic compound - N-arylamide - Benzoyl - Halobenzene - Fluorobenzene - Fatty amide - Benzenoid - Fatty acyl - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Carboxamide group - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organic oxoazanium - Hydrocarbon derivative - Organic zwitterion - Organic oxide - Organic oxygen compound - Carbonyl group - Organic salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organic nitrogen compound - Organofluoride - 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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