Structure Information
Structure

Compound Identification

SMILES

CN[C@@](CC1=CC=CCC1)(N(N1C2=C(C=C(Cl)C=C2)C(=NC(C(=O)C(N)CS)C1=O)C1=CC=CC=C1)C(C)=O)C(O)=O

InChIKey

InChIKey=FTXANZGJCBJDMX-GRFFYOSDSA-N

Formula

C30H32ClN5O5S

Mass

610.13

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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 - N-acyl-alpha amino acids and derivatives - N-acyl-alpha amino acids

Direct Parent

N-acyl-L-alpha-amino acids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-acyl-l-alpha-amino acid - Benzodiazepine - 1,4-benzodiazepine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - 1,3-dicarbonyl compound - Benzenoid - Alpha-aminoketone - Acetamide - Amino acid - Carboxylic acid hydrazide - Ketimine - Ketone - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Azacycle - Alkylthiol - Carboxylic acid - Monocarboxylic acid or derivatives - Primary amine - Primary aliphatic amine - Amine - Imine - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organochloride - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.

External Descriptors

Not available

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