Title of article
Bioorganic synthesis of end-capped anti-HIV peptides by simultaneous cyanocysteine-mediated cleavages of recombinant proteins Original Research Article
Author/Authors
Michinori Tanaka، نويسنده , , Kazumi Kajiwara، نويسنده , , Rei Tokiwa، نويسنده , , Kentaro Watanabe، نويسنده , , Hiroaki Ohno، نويسنده , , Hiroko Tsutsumi، نويسنده , , Yoji Hata، نويسنده , , Kazuki Izumi، نويسنده , , Eiichi Kodama، نويسنده , , Masao Matsuoka، نويسنده , , Shinya Oishi، نويسنده , , Nobutaka Fujii*، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
6
From page
7487
To page
7492
Abstract
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.
Keywords
Bioorganic synthesis , End-capped peptide , Fusion inhibitor , HIV-1
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2009
Journal title
Bioorganic and Medicinal Chemistry
Record number
1306495
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