Synthesis of Novel Histidine-based Open-chain Dipeptides, Polypeptides and Cyclopeptides with Anti-HIV Potential  

作　　者：ZHOU Cheng-He LIU Qiang Juan F. Miravet M. Isabel Burguete Santiago V. Luis 

机构地区：[1]Laboratory of Bioorganic and Medicinal Chemistry, School of Pharmaceutical Sciences, Chongqing University of Medical Sciences, Chongqing 400016 [2]Department of Inorganic and Organic Chemistry, Universitat Jaume I, Castellon 12080, Spain Laboratory of Bioorganic and Medicinal Chemistry, School of Pharmaceutical Sciences, Chongqing University of Medical Sciences, Chongqing 400016 Department of Inorganic and Organic Chemistry, Universitat Jaume I, Castellon 12080, Spain Department of Inorganic and Organic Chemistry, Universitat Jaume I, Castellon 12080, Spain Department of Inorganic and Organic Chemistry, Universitat Jaume I, Castellon 12080, Spain

出　　处：《有机化学》2003年第z1期415-415,共1页Chinese Journal of Organic Chemistry

基　　金：Project supported by the National Natural Science Foundation of China, the Personnel Department of China, Sciences and Technology Committee ofChongqing as well as the Foundation for Foreign Scientists from the Ministry of Spanish Culture and Education (No.SB9751204311).

摘　　要：　　A series of novel histidine-based open-chain dipeptides, polypeptides and cyclopeptides with anti-HIV potential were designed and synthesized from commercial histidine (Scheme 1).……

分 类 号：O62[理学—有机化学]