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2. Irreversible enzyme inhibitors. 113. Proteolytic enzymes. 3. Active-site-directed irreversible inhibitors of alpha-chymotrypsin derived from phenoxyacetamides with an N-fluorosulfonylphenyl substituent. Baker BR, Hurlbut JA. J Med Chem; 1968 Mar; 11(2):233-41. PubMed ID: 5654208 [No Abstract] [Full Text] [Related]
3. Irreversible enzyme inhibitors. CXIV. Proteolytic enzymes. IV. Additional active-site-directed irreversible inhibitors of alpha-chymotrypsin derived from phenoxyacetamides bearing a terminal sulfonyl fluoride. Baker BR, Hurlbut JA. J Med Chem; 1968 Mar; 11(2):241-5. PubMed ID: 5654209 [No Abstract] [Full Text] [Related]
4. Irreversible enzyme inhibitors. CXLV. Proteolytic enzymes. 8. Active-site-directed irreversible inhibitors of alpha-chymotrypsin derived from alpha-(2-carboxy-4-chlorophenoxy)acetamide bearing a terminal sulfonyl fluoride. Baker BR, Hurlbut JA. J Med Chem; 1969 Jan; 12(1):118-22. PubMed ID: 5763006 [No Abstract] [Full Text] [Related]
5. Irreversible enzyme inhibitors. CXXXII. Proteolytic enzymes. VI. Tolerance for polar groups on the phenoxyacetanilide type of inhibitor of alpha-chymotrypsin. Baker BR, Hurlbut JA. J Med Chem; 1968 Sep; 11(5):1054-9. PubMed ID: 5697070 [No Abstract] [Full Text] [Related]
6. INTERACTION OF AROMATIC COMPOUNDS WITH ALPHA-CHYMOTRYPSIN. WALLACE RA, KURTZ AN, NIEMANN C. Biochemistry; 1963 Sep; 2():824-36. PubMed ID: 14075122 [No Abstract] [Full Text] [Related]
11. Irreversible enzyme inhibitors. CLXI. Proteolytic enzymes. 13. Inhibitors of guinea pig complement derived by quaternization of 3-acylamidopyridines with alpha-bromomethylbenzenesulfonyl fluorides. II. Baker BR, Hurlbut JA. J Med Chem; 1969 Sep; 12(5):902-5. PubMed ID: 5812209 [No Abstract] [Full Text] [Related]
12. Microenvironmental effects on enzyme catalysis. A kinetic study of polyanionic and polycationic derivatives of chymotrypsin. Goldstein L. Biochemistry; 1972 Oct 24; 11(22):4072-84. PubMed ID: 5086538 [No Abstract] [Full Text] [Related]
13. [Correlation of enzyme thermostability and its surface hydrophobicity (using a modified alpha-chymotrypsin as an example)]. Melik-Nubarov NS, Shikshnis VA, Slepnev VI, Shchegolev AA, Mozhaev VV. Mol Biol (Mosk); 1990 Oct 24; 24(2):346-57. PubMed ID: 2362586 [Abstract] [Full Text] [Related]
14. INTERACTION OF AROMATIC COMPOUNDS WITH ALPHA-CHYMOTRYPSIN. II. COMBINATION OF THE ISOMERIC INDOLE CARBOXAMIDES AND CARBOXYLATE IONS WITH THE ACTIVE SITE. ABRASH HI, NIEMANN C. Biochemistry; 1965 Jan 24; 4():99-104. PubMed ID: 14285251 [No Abstract] [Full Text] [Related]
17. The binding of inhibitors to alpha-chymotrypsin. Johnson CH, Knowles JR. Biochem J; 1966 Oct 24; 101(1):56-62. PubMed ID: 5971792 [Abstract] [Full Text] [Related]