Structure Information
Structure

Compound Identification

SMILES

CN(C)C(=O)[C@H](CC1=CC=C(C=C1)N1C(=O)N(C)C2=CC=CC=C2C1=O)NC(=O)C1=C(Cl)C=CC=C1Cl

InChIKey

InChIKey=MOALKSHAUVZOQT-NRFANRHFSA-N

Formula

C27H24Cl2N4O4

Mass

539.41

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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

Phenylalanine and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phenylalanine or derivatives - N-acyl-alpha amino acid or derivatives - Hippuric acid or derivatives - Alpha-amino acid amide - Diazanaphthalene - Amphetamine or derivatives - Quinazoline - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzamide - Benzoic acid or derivatives - 1,3-dichlorobenzene - Benzoyl - Halobenzene - Chlorobenzene - Pyrimidone - Monocyclic benzene moiety - Aryl chloride - Pyrimidine - Aryl halide - Benzenoid - Vinylogous amide - Heteroaromatic compound - Tertiary carboxylic acid amide - Vinylogous halide - Urea - Secondary carboxylic acid amide - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine 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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