Structure Information
Structure

Compound Identification

SMILES

NCCCCCCN(CC(N)=O)C(=O)CN(CCCCCCN)C(=O)CN(CCCCCCN)C(=O)CN(CCCCCCN)C(=O)CN(CCCCCCN)C(=O)CCCCCNC(=O)C1=CC(C(O)=O)=C(C=C1)C1=C2C=CC(=O)C=C2OC2=C1C=CC(O)=C2

InChIKey

InChIKey=KTSOBEAUASSRDS-UHFFFAOYSA-N

Formula

C67H104N12O12

Mass

1269.641

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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 heteropolycyclic compounds

Substituents

Peptoid - Dibenzopyran - Xanthene - Alpha-amino acid or derivatives - Benzopyran - 1-benzopyran - Benzamide - Benzoic acid or derivatives - Benzoic acid - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - N-acyl-amine - Benzenoid - Tertiary carboxylic acid amide - Heteroaromatic compound - Secondary carboxylic acid amide - Primary carboxylic acid amide - Cyclic ketone - Amino acid or derivatives - Amino acid - Carboxamide group - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Primary amine - Primary aliphatic amine - Carbonyl group - Hydrocarbon derivative - Amine - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic 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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