Structure Information
Structure

Compound Identification

SMILES

[Br-].[Br-].CN(CC(=O)N(C)CC(=O)N1CC[N+](CC2=CC=CC=C2)(CC2=CC=C(C=C2)[N+]([O-])=O)CC1)C(=O)C[N+]1(CC2=CC=C(C=C2)[N+]([O-])=O)CCCCC1

InChIKey

InChIKey=LXAPDBJEEYZZDA-UHFFFAOYSA-L

Formula

C38H49Br2N7O7

Mass

875.66

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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 - N-benzylpiperidine - Benzylpiperidine - Alpha-amino acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzylamine - Phenylmethylamine - Aralkylamine - N-alkylpiperazine - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Piperidine - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Tertiary carboxylic acid amide - Carboxamide group - Organic nitro compound - C-nitro compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Organic oxide - Organic bromide salt - Amine - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic zwitterion - 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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