Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)N(CC(=O)N(C)CC(O)=O)C(=O)C1=CC=C(Cl)C=C1

InChIKey

InChIKey=OCCCHHSSTSPVRC-UHFFFAOYSA-N

Formula

C19H19ClN2O5

Mass

390.82

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Peptidomimetics

Subclass

Peptoids

Intermediate Tree Nodes

Not available

Direct Parent

Peptoids

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Peptoid - Alpha-dipeptide - Benzanilide - Aromatic anilide - Hippuric acid or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzoic acid or derivatives - Benzamide - Methoxyaniline - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Alkyl aryl ether - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Aryl chloride - Aryl halide - Benzenoid - Tertiary carboxylic acid amide - Carboxamide group - Carboxylic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Organic nitrogen compound - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as peptoids. These are peptidomimetics made of N-substituted amino acids, in which the side chains are attached to the nitrogen atom of the peptide backbone, rather than to the alpha-carbons. Alpha-peptoids (commonly referred to as peptoids) are N-substituted glycines. But in general, this class also extends to oligo- or polymers of beta-, gamma-, delta peptoid analogues of amino acids.

External Descriptors

Not available

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