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pubmed-article:19811922pubmed:abstractTextBioorganic 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.lld:pubmed
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pubmed-article:19811922pubmed:articleTitleBioorganic synthesis of end-capped anti-HIV peptides by simultaneous cyanocysteine-mediated cleavages of recombinant proteins.lld:pubmed
pubmed-article:19811922pubmed:affiliationGraduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan.lld:pubmed
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