Homoarginine Oligomers as Trypsin and Chymotrypsin Substrates and Inhibitors
Autor: | Y. Elkana, N. Segal, L. Schwartz, M. Rigbi, D. Kliger |
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Rok vydání: | 1974 |
Předmět: | |
Zdroj: | Bayer-Symposium ISBN: 9783642879685 |
Popis: | The object of this work was to obtain synthetic, reversible trypsin inhibitors. The work is based on a consideration of the length of the positively-charged amino acid side-chain which makes its ester, amide or peptide bond most susceptible to cleavage by trypsin. It is well-known that between the positively-charged atom and the α-carbon, four atoms are optimal. |
Databáze: | OpenAIRE |
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