Click Chemistry for Drug Development and Diverse Chemical-Biology Applications

被引:1625
作者
Thirumurugan, Prakasam [1 ]
Matosiuk, Dariusz [2 ]
Jozwiak, Krzysztof [1 ]
机构
[1] Med Univ Lublin, Dept Chem, Lab Med Chem & Neuroengn, PL-20093 Lublin, Poland
[2] Med Univ Lublin, Dept Synth & Chem Technol Pharmaceut Subst, PL-20093 Lublin, Poland
关键词
PROTEIN-TYROSINE-PHOSPHATASE; AZIDE-ALKYNE CYCLOADDITION; A(3) ADENOSINE RECEPTOR; ACTIVITY-BASED PROBES; CARBONIC-ANHYDRASE INHIBITORS; N-SUBSTITUTED AMINOCYCLITOLS; NEWLY SYNTHESIZED PROTEINS; SMALL-MOLECULE INHIBITORS; COPPER-FREE; IN-VIVO;
D O I
10.1021/cr200409f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Researchers explore the potential of click chemistry for drug development and diverse chemical-biology applications. Click chemistry is a newer approach to the synthesis of drug-like molecules that can accelerate the drug discovery process by utilizing a few practical and reliable reactions. Researchers have defined the click reaction as wide in scope and easy to perform, which uses only readily available reagents and is insensitive to oxygen and water. Some of the attributes of click reactions include many of these components being derived from derived from alkenes and alkynes, along with from the cracking of petroleum and many of these reactions involve the formation of carbon-heteroatom bonds. Click chemistry-based drug discovery are mainly of three types, such as high-throughput screening, fragment-based drug discovery, and dynamic template-assisted strategies in fragment-based drug discovery.
引用
收藏
页码:4905 / 4979
页数:75
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