Syntheses of derivatives of N2-acetyl-N3-glycyl-L-2,3-diaminopropionic acid and their hydrolyses by trypsin.
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概要
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Amide and ethyl ester of <I>N</I><SUP>2</SUP>-acetyl-<I>N</I><SUP>3</SUP>-glycyl-L-2,3-diaminopropionic acid replacing an ethylene group in the side chain of lysine by a peptide bond were synthesized. The susceptibility of each derivative to trypsin was compared with that of the corresponding <I>N</I><SUP>2</SUP>-acetyl-L-lysine derivative. Each derivative was hydrolyzed by trypsin, but was less susceptible than the corresponding L-lysine derivative.
- 公益社団法人 日本化学会の論文
著者
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Waki Michinori
Laboratory Of Biochemistry Department Of Chemistry Faculty Of Science Kyushu University
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Izumiya Nobuo
Laboratory Of Biochemistry Faculty Of Engineering Kyushu Sangyo University
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KATO Tetsuo
Laboratory of Biochemistry, Faculty of Science, Kyushu University
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Minematsu Yoshihiro
Laboratory of Biochemistry, Faculty of Science 33, Kyushu University
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Minematsu Yoshihiro
Laboratory of Biochemistry, Faculty of Science, Kyushu University 33
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Kang Shinwon
Laboratory of Biochemistry, Faculty of Science, Kyushu University 33
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