Use of Click-Chemistry in the Development of Peptidomimetic Enzyme Inhibitors

2014 ◽  
Vol 21 (13) ◽  
pp. 1467-1477 ◽  
Author(s):  
P. Fabbrizzi ◽  
G. Menchi ◽  
A. Guarna ◽  
A. Trabocchi
2004 ◽  
Vol 126 (40) ◽  
pp. 12809-12818 ◽  
Author(s):  
Roman Manetsch ◽  
Antoni Krasiński ◽  
Zoran Radić ◽  
Jessica Raushel ◽  
Palmer Taylor ◽  
...  

2007 ◽  
Vol 2 (11) ◽  
pp. 2655-2664 ◽  
Author(s):  
Rajavel Srinivasan ◽  
Junqi Li ◽  
Su Ling Ng ◽  
Karunakaran A Kalesh ◽  
Shao Q Yao

RSC Advances ◽  
2015 ◽  
Vol 5 (13) ◽  
pp. 9965-9972 ◽  
Author(s):  
A. Sandomenico ◽  
V. Celentano ◽  
L. D. D'Andrea ◽  
G. Palmieri ◽  
M. Ruvo

Peptide-engrafted triazoles, obtained via click chemistry, drive the inhibition activity toward Acyl Peptide Hydrolase (APEH), a modulator of the proteasome activity.


2011 ◽  
Vol 346 (1) ◽  
pp. 16-25 ◽  
Author(s):  
Namarata Anand ◽  
Natasha Jaiswal ◽  
Sarvesh Kumar Pandey ◽  
A.K. Srivastava ◽  
Rama P. Tripathi

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5368
Author(s):  
Tingting Yao ◽  
Xiaowei Xu ◽  
Rong Huang

Despite significant advances in biological and analytical approaches, a comprehensive portrait of the proteome and its dynamic interactions and modifications remains a challenging goal. Chemical proteomics is a growing area of chemical biology that seeks to design small molecule probes to elucidate protein composition, distribution, and relevant physiological and pharmacological functions. Click chemistry focuses on the development of new combinatorial chemical methods for carbon heteroatom bond (C-X-C) synthesis, which have been utilized extensively in the field of chemical proteomics. Click reactions have various advantages including high yield, harmless by-products, and simple reaction conditions, upon which the molecular diversity can be easily and effectively obtained. This paper reviews the application of click chemistry in proteomics from four aspects: (1) activity-based protein profiling, (2) enzyme-inhibitors screening, (3) protein labeling and modifications, and (4) hybrid monolithic column in proteomic analysis.


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