N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester Mixture of hydrochloride and hydrobromide
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N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester Mixture of hydrochloride and hydrobromide

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Category
CBZ-Amino Acids
Catalog number
BAT-001459
CAS number
96723-72-7
Molecular Formula
C21H27BrClN5O6
Molecular Weight
560.84
N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester Mixture of hydrochloride and hydrobromide
IUPAC Name
(4-nitrophenyl)methyl (2S)-5-(diaminomethylideneamino)-2-(phenylmethoxycarbonylamino)pentanoate;hydrochloride
Synonyms
Z-Arg-OBzl(4-NO2) HCl HBr
Purity
99%
Storage
Store at RT
InChI
InChI=1S/C21H25N5O6.ClH/c22-20(23)24-12-4-7-18(25-21(28)32-14-15-5-2-1-3-6-15)19(27)31-13-16-8-10-17(11-9-16)26(29)30;/h1-3,5-6,8-11,18H,4,7,12-14H2,(H,25,28)(H4,22,23,24);1H/t18-;/m0./s1
InChI Key
NZOFENWQBGWSEU-FERBBOLQSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CCCN=C(N)N)C(=O)OCC2=CC=C(C=C2)[N+](=O)[O-].Cl

N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester, a compound utilized in a myriad of biochemical research applications, serves as a substrate for high perplexity and burstiness in the following key applications:

Protease Inhibition Studies: This compound, integral to studies on protease enzymes, acts as a substrate enabling researchers to delve into the intricate interactions between proteases and N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester. Through this exploration, insights into enzyme kinetics and mechanisms are uncovered, laying the foundation for the development of protease inhibitors as therapeutic entities.

Biochemical Assays: In the realm of biochemical assays, N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester emerges as a crucial tool for measuring enzymatic activity. Its utilization aids in quantifying the activities of diverse arginine-specific proteases, thereby shedding light on enzyme functionality and potential inhibitory factors. These assays play a pivotal role in the realms of drug discovery and enzyme characterization.

Peptide Synthesis: Additionally, this compound assumes a vital role in peptide synthesis by serving as a safeguarding entity for the arginine side chain. Through shielding reactive groups during the synthetic process, it ensures the precise formation of desired peptide bonds, crucial for the production of synthetic peptides utilized in both research and therapeutic applications.

Structural Biology: Within the realm of structural biology, researchers leverage N-α-Carbobenzoxy-L-arginine p-nitrobenzyl ester to unravel the intricate structural features of proteins. By manipulating specific residues, scientists embark on an exploration of conformational shifts and protein dynamics. This methodology deepens our comprehension of protein structure-function correlations, thereby facilitating the design of innovative proteins and biomolecules.

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