期刊
BIOORGANIC & MEDICINAL CHEMISTRY
卷 17, 期 21, 页码 7487-7492出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2009.09.015
关键词
Bioorganic synthesis; End-capped peptide; Fusion inhibitor; HIV-1
资金
- Japan Science and Technology Agency
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Health and Labour Sciences Research
Bioorganic synthesis of N- and C-terminal end-capped peptides by two simultaneous S-cyanocysteine-mediated cleavages of recombinant proteins is described. This approach is demonstrated in the preparation of anti-HIV fusion inhibitory peptides. (C) 2009 Elsevier Ltd. All rights reserved.
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