Structure Information
Structure

Compound Identification

SMILES

CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@@H](CC(=O)N(CC(=O)N(C)CCC(=O)N1CCOCC1)[C@@H](C)C1=CC=CC=C1)CC1=CSC(N)=N1

InChIKey

InChIKey=PQKPWZBQCXPGFF-XZYRSLMWSA-N

Formula

C40H62N6O7S

Mass

771.03

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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 heteromonocyclic compounds

Substituents

Peptoid - Beta amino acid or derivatives - Alpha-amino acid or derivatives - 2,4-disubstituted 1,3-thiazole - N-acyl-amine - Morpholine - Monocyclic benzene moiety - 1,3-thiazol-2-amine - Fatty acyl - Oxazinane - Benzenoid - Fatty amide - Azole - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Alcohol - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic 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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