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Structure Information
Structure

Compound Identification

SMILES

CC1=NN(C(=O)C1N=NC1=CC=C(NC2=C(Cl)C(F)=NC(F)=N2)C=C1)C1=C(C=CC(=C1)S(O)(=O)=O)S(O)(=O)=O

InChIKey

InChIKey=KXQHRWALALFEOE-UHFFFAOYSA-N

Formula

C20H14ClF2N7O7S2

Mass

601.94

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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

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Alpha-amino acid or derivatives - Benzenesulfonate - 1-sulfo,2-unsubstituted aromatic compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Aniline or substituted anilines - Halopyrimidine - 2-halopyrimidine - Aminopyrimidine - Pyrazolinone - Aryl halide - Aryl chloride - Imidolactam - Pyrimidine - Monocyclic benzene moiety - Benzenoid - Aryl fluoride - Pyrazoline - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Sulfonyl - Heteroaromatic compound - Azo compound - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Organohalogen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

External Descriptors

Not available

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