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Sku CI06204_5_G
Chem Impex
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Product Information

Product Name
L-Proline 4-nitroanilide hydrobromide
Brand Name
Chem Impex
Product Number
06204
CAS
7369-91-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7408106
IUPAC Name
(2S)-N-(4-nitrophenyl)pyrrolidine-2-carboxamide
InChI Key
JWXPYNYNEUYKOW-JTQLQIEISA-N
SMILES
C1CC@H(NC1)C(=O)NC2=CC=C(C=C2)N+(=O)O-

Application

L-Proline 4-nitroanilide hydrobromide is widely utilized in research focused on:

Protein Synthesis: This compound serves as a useful reagent in the synthesis of peptides and proteins, aiding researchers in studying protein structure and function.

Enzyme Activity Studies: It is employed in assays to evaluate enzyme activity, particularly in the context of proteases, providing insights into biochemical pathways.

Drug Development: The compound is explored in pharmaceutical research for its potential as a lead compound in the development of new therapeutic agents, particularly in targeting specific biological pathways.

Analytical Chemistry: It is used in chromatography and spectrometry for the analysis of amino acids and peptides, enhancing accuracy in quantitative assessments.

Biochemical Research: The compound plays a role in studying metabolic processes, contributing to a better understanding of cellular functions and disease mechanisms.

References Data Source From Pubchem

Characterization of an Aminopeptidase and a Proline Iminopeptidase from Cabbage Leaves

Publication Name: Zeitschrift fur Naturforschung. C, Journal of biosciences
Publication Date: 2008-02-01
DOI: 10.1515/znc-2008-1-220

An Aneurinibacillus sp. strain AM-1 produces a proline-specific aminopeptidase useful for collagen degradation

Publication Name: Journal of Applied Microbiology
Publication Date: 2004-04
DOI: 10.1111/j.1365-2672.2004.02210.x

The peptidolytic capacity of the spirochete system

Publication Name: Medical Microbiology and Immunology
Publication Date: 1996-06
DOI: 10.1007/s004300050008

Development of selective tight-binding inhibitors of leukotriene A4 hydrolase

Publication Name: Journal of Medicinal Chemistry
Publication Date: 1993-01-22
DOI: 10.1021/jm00054a004