KINETICS OF INACTIVATION OF ALPHA-CHYMOTRYPSIN WITH SUBSTITUTED BENZENESULFONYL FLUORIDES

[1] IRREVERSIBLE ENZYME INHIBITORS .128. P-(4,6-DIAMINO-1,2-DIHYDRO-2,2-DIMETHYL-S-TRIAZIN-1-YL)PHENYLPROPIONYLSULFANILYL FLUORIDE AN ACTIVE-SITE-DIRECTED IRREVERSIBLE INHIBITOR OF DIHYDROFOLIC REDUCTASE .4. EFFECTS OF SUBSTITUTION ON PROPIONAMIDE BRIDGE ON ISOZYME SPECIFICITY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1968, 11 (04) : 672 - &

[2] IRREVERSIBLE ENZYME INHIBITORS .113. PROTEOLYTIC ENZYMES .3. ACTIVE-SITE-DIRECTED IRREVERSIBLE INHIBITORS OF ALPHA-CHYMOTRYPSIN DERIVED FROM PHENOXYACETAMIDES WITH AN N-FLUOROSULFONYLPHENYL SUBSTITUENT [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1968, 11 (02) : 233 - &

[3] ON INTERACTION OF ACTIVE SITE OF ALPHA-CHYMOTRYPSIN WITH CHROMOPHORES - PROFLAVIN BINDING AND ENZYME CONFORMATION DURING CATALYSIS [J]. JOURNAL OF MOLECULAR BIOLOGY, 1966, 18 (03) : 405 - &

[4] ATOMIC CO-ORDINATES FOR TOSYL-ALPHA-CHYMOTRYPSIN [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1969, 36 (01) : 131 - &

[5] STRUCTURE OF CRYSTALLINE ALPHA-CHYMOTRYPSIN .5. ATOMIC STRUCTURE OF TOSYL-ALPHA-CHYMOTRYPSIN AT 2 A RESOLUTION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1972, 68 (02) : 187 - &

[6] Blow D.M., 1971, The Enzymes, V3, P185, DOI DOI 10.1016/S1874-6047(08)60397-2

[7] BRANDT KG, 1967, J BIOL CHEM, V242, P3973

[8] BRUICE TC, 1966, BIOORGANIC MECHANISM, V1, pCH2

[9] TRANSIENT FORMATION OF A COMPLEX BETWEEN ALPHA-CHYMOTRYPSIN, PROFLAVIN, AND TOSYLARGININE METHYL-ESTER (TAME) [J]. CANADIAN JOURNAL OF BIOCHEMISTRY, 1972, 50 (03): : 257 - +

[10] DECAT AH, 1963, J ORG CHEM, V28, P3426

[1] IRREVERSIBLE ENZYME INHIBITORS .128. P-(4,6-DIAMINO-1,2-DIHYDRO-2,2-DIMETHYL-S-TRIAZIN-1-YL)PHENYLPROPIONYLSULFANILYL FLUORIDE AN ACTIVE-SITE-DIRECTED IRREVERSIBLE INHIBITOR OF DIHYDROFOLIC REDUCTASE .4. EFFECTS OF SUBSTITUTION ON PROPIONAMIDE BRIDGE ON ISOZYME SPECIFICITY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1968, 11 (04) : 672 - &

[2] IRREVERSIBLE ENZYME INHIBITORS .113. PROTEOLYTIC ENZYMES .3. ACTIVE-SITE-DIRECTED IRREVERSIBLE INHIBITORS OF ALPHA-CHYMOTRYPSIN DERIVED FROM PHENOXYACETAMIDES WITH AN N-FLUOROSULFONYLPHENYL SUBSTITUENT [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1968, 11 (02) : 233 - &

[3] ON INTERACTION OF ACTIVE SITE OF ALPHA-CHYMOTRYPSIN WITH CHROMOPHORES - PROFLAVIN BINDING AND ENZYME CONFORMATION DURING CATALYSIS [J]. JOURNAL OF MOLECULAR BIOLOGY, 1966, 18 (03) : 405 - &

[4] ATOMIC CO-ORDINATES FOR TOSYL-ALPHA-CHYMOTRYPSIN [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1969, 36 (01) : 131 - &

[5] STRUCTURE OF CRYSTALLINE ALPHA-CHYMOTRYPSIN .5. ATOMIC STRUCTURE OF TOSYL-ALPHA-CHYMOTRYPSIN AT 2 A RESOLUTION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1972, 68 (02) : 187 - &

[6] Blow D.M., 1971, The Enzymes, V3, P185, DOI DOI 10.1016/S1874-6047(08)60397-2

[7] BRANDT KG, 1967, J BIOL CHEM, V242, P3973

[8] BRUICE TC, 1966, BIOORGANIC MECHANISM, V1, pCH2

[9] TRANSIENT FORMATION OF A COMPLEX BETWEEN ALPHA-CHYMOTRYPSIN, PROFLAVIN, AND TOSYLARGININE METHYL-ESTER (TAME) [J]. CANADIAN JOURNAL OF BIOCHEMISTRY, 1972, 50 (03): : 257 - +

[10] DECAT AH, 1963, J ORG CHEM, V28, P3426