| Year |
Citation |
Score |
| 1996 |
CLEMENT GE, BENDER ML. THE EFFECT OF APROTIC DIPOLAR ORGANIC SOLVENTS ON THE KINETICS OF ALPHA-CHYMOTRYPSIN-CATALYZED HYDROLYSES. Biochemistry. 2: 836-43. PMID 14075123 DOI: 10.1021/Bi00904A036 |
0.33 |
|
| 1996 |
BENDER ML, CLEMENT GE. KINETIC EVIDENCE FOR AN ACYL-ENZYME INTERMEDIATE IN THE ALPHA-CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF N-ACETYL-L-TRYPTOPHAN ETHYL ESTER. Biochemical and Biophysical Research Communications. 12: 339-44. PMID 14070341 DOI: 10.1016/0006-291X(63)90308-5 |
0.408 |
|
| 1987 |
Bender ML. Kinetic studies of immobilized alpha-chymotrypsin in aprotic solvents. Methods in Enzymology. 135: 537-46. PMID 3600308 DOI: 10.1016/0076-6879(87)35109-2 |
0.389 |
|
| 1987 |
D'Souza VT, Lu XL, Ginger RD, Bender ML. Thermal and pH stability of "beta-benzyme". Proceedings of the National Academy of Sciences of the United States of America. 84: 673-4. PMID 3468505 DOI: 10.1073/Pnas.84.3.673 |
0.633 |
|
| 1987 |
Wu HL, Shi GY, Bender ML. Preparation and purification of microplasmin. Proceedings of the National Academy of Sciences of the United States of America. 84: 8292-5. PMID 2960974 DOI: 10.1073/Pnas.84.23.8292 |
0.304 |
|
| 1987 |
D'Souza VT, Bender ML. Miniature organic models of enzymes Accounts of Chemical Research. 20: 146-152. DOI: 10.1021/Ar00136A004 |
0.676 |
|
| 1986 |
Bender ML, D'Souza VT, Lu X. Miniature, organic models of chymotrypsin based on α-, β- and γ-cyclodextrins Trends in Biotechnology. 4: 132-135. DOI: 10.1016/0167-7799(86)90161-7 |
0.644 |
|
| 1985 |
D'Souza VT, Hanabusa K, O'Leary T, Gadwood RC, Bender ML. Synthesis and evaluation of a miniature organic model of chymotrypsin. Biochemical and Biophysical Research Communications. 129: 727-32. PMID 4015652 DOI: 10.1016/0006-291X(85)91952-7 |
0.679 |
|
| 1984 |
Tsai IH, Bender ML. Inhibition of porcine elastase and anhydroelastase by boronic acids. Archives of Biochemistry and Biophysics. 228: 555-9. PMID 6559567 DOI: 10.1016/0003-9861(84)90022-5 |
0.36 |
|
| 1984 |
Mallick IM, D'Souza VT, Yamaguchi M, Lee J, Chalabi P, Gadwood RC, Bender ML. An organic chemical model of the acyl-.alpha.-chymotrypsin intermediate Journal of the American Chemical Society. 106: 7252-7254. DOI: 10.1021/Ja00335A070 |
0.665 |
|
| 1984 |
Komiyama M, Bender ML. Chapter 14 Cyclodextrins as enzyme models New Comprehensive Biochemistry. 6: 505-527. DOI: 10.1016/S0167-7306(08)60385-3 |
0.384 |
|
| 1984 |
Bender ML. An artificial acyl-enzyme and an artificial enzyme Journal of Inclusion Phenomena. 2: 433-444. DOI: 10.1007/978-94-009-5376-5_48 |
0.388 |
|
| 1984 |
Mallick IM, D'Souza VT, Yamaguchi M, Lee J, Chalabi P, Gadwood RC, Bender ML. An organic chemical model of the acyl-α-chymotrypsin intermediate Journal of the American Chemical Society. 106: 7252-7254. DOI: 10.1002/Chin.198511334 |
0.303 |
|
| 1983 |
Amshey JW, Bender ML. Fluorine magnetic resonance studies of fluorine-substituted benzoyl chymotrypsins. Archives of Biochemistry and Biophysics. 224: 378-81. PMID 6870262 DOI: 10.1016/0003-9861(83)90223-0 |
0.301 |
|
| 1982 |
Wu HL, Kundrot C, Bender ML. The denaturation of trypsin. Biochemical and Biophysical Research Communications. 107: 742-5. PMID 7126237 DOI: 10.1016/0006-291X(82)91553-4 |
0.333 |
|
| 1981 |
Wu HL, Lace DA, Bender ML. Elimination of cannibalistic denaturation by enzyme immobilization or inhibition. Proceedings of the National Academy of Sciences of the United States of America. 78: 4118-9. PMID 16593052 DOI: 10.1073/Pnas.78.7.4118 |
0.396 |
|
| 1981 |
Wu HL, Wastell A, Bender ML. Ageing of alpha-chymotrypsin: Cannibalistic and hydroxide ion reactions. Proceedings of the National Academy of Sciences of the United States of America. 78: 4116-7. PMID 16593051 DOI: 10.1073/Pnas.78.7.4116 |
0.415 |
|
| 1980 |
Komiyama M, Bender ML. The Cyclodextrin-accelerated Cleavage of ThiocarboxylicS-Esters Bulletin of the Chemical Society of Japan. 53: 1073-1076. DOI: 10.1246/Bcsj.53.1073 |
0.313 |
|
| 1980 |
Philipp M, Tsai I, Bender M. Corrections - Comparison of the Kinetic Specificity of Subtilisin and Thiolsubtilisin toward η-Alkyl p-Nitrophenyl Esters Biochemistry. 19: 4385-4385. DOI: 10.1021/Bi00559A600 |
0.311 |
|
| 1980 |
Komiyama M, Bender ML. Proton inventory study of the general base-catalyzed hydrolyses of trifluoroacetanilides by imidazole Bioorganic Chemistry. 9: 288-292. DOI: 10.1016/0045-2068(80)90037-1 |
0.345 |
|
| 1979 |
Tsai IH, Bender ML. Conformation of the active site of thiolsubtilisin: reaction with specific chloromethyl ketones and arylacryloylimidazoles. Biochemistry. 18: 3764-8. PMID 476086 DOI: 10.1021/Bi00584A019 |
0.351 |
|
| 1979 |
Komiyama M, Bender ML. Do cleavages of amides by serine proteases occur through a stepwise pathway involving tetrahedral intermediates? Proceedings of the National Academy of Sciences of the United States of America. 76: 557-60. PMID 284381 DOI: 10.1073/Pnas.76.2.557 |
0.385 |
|
| 1979 |
Philipp M, Tsai IH, Bender ML. Comparison of the kinetic specificity of subtilisin and thiolsubtilisin toward n-alkyl p-nitrophenyl esters. Biochemistry. 18: 3769-73. PMID 38838 DOI: 10.1021/Bi00584A020 |
0.407 |
|
| 1979 |
Grooms TA, Bender ML. Modification, purification, and characterization of an enzyme with altered specificity Journal of Molecular Catalysis. 6: 359-366. DOI: 10.1016/0304-5102(79)85011-7 |
0.364 |
|
| 1979 |
Komiyama M, Bender ML. Nucleophilic acceleration of the cleavage of β-cyclodextrin trans-cinnamate by amines Bioorganic Chemistry. 8: 249-254. DOI: 10.1016/0045-2068(79)90010-5 |
0.393 |
|
| 1978 |
Nayak PL, Bender ML. Organophosphorus compounds as active site-directed inhibitors of elastase. Biochemical and Biophysical Research Communications. 83: 1178-82. PMID 568468 DOI: 10.1016/0006-291X(78)91519-X |
0.307 |
|
| 1978 |
Komiyama M, Bender ML. Thermodynamic studies of the cyclodextrin-accelerated cleavage of phenyl esters Journal of the American Chemical Society. 100: 4576-4579. DOI: 10.1021/Ja00482A042 |
0.323 |
|
| 1978 |
Komiyama M, Bender ML. Hydrolysis of p-nitrotrifluoroacetanilide catalyzed by water and imidazole Bioorganic Chemistry. 7: 133-139. DOI: 10.1016/0045-2068(78)90044-5 |
0.337 |
|
| 1977 |
Bender ML, Cottingham AB, Sun LK, Tanizawa K. Kinetic studies of immobilized alpha-chymotrypsin in apolar solvents. Advances in Experimental Medicine and Biology. 86: 405-13. PMID 21537 DOI: 10.1007/978-1-4684-3282-4_25 |
0.389 |
|
| 1977 |
Komiyama M, Bender ML, Utaka M, Takeda A. Model for "charge-relay": acceleration by carboxylate anion in intramolecular general base-catalyzed ester hydrolysis by the imidazolyl group. Proceedings of the National Academy of Sciences of the United States of America. 74: 2634-8. PMID 19738 DOI: 10.1073/Pnas.74.7.2634 |
0.339 |
|
| 1977 |
Hirohara H, Philipp M, Bender ML. Binding rates, O--S substitution effects, and the pH dependence of chymotrypsin reactions. Biochemistry. 16: 1573-80. PMID 15586 DOI: 10.1021/Bi00627A007 |
0.326 |
|
| 1977 |
Komiyama M, Roesel TR, Bender ML. Intramolecular general base-catalyzed ester hydrolyses by the imidazolyl group. Proceedings of the National Academy of Sciences of the United States of America. 74: 23-5. PMID 13364 DOI: 10.1073/Pnas.74.1.23 |
0.327 |
|
| 1977 |
Komiyama M, Bender ML. Cyclodextrin-catalyzed hydrolyses of acetanilides Journal of the American Chemical Society. 99: 8021-8024. DOI: 10.1021/Ja00466A040 |
0.414 |
|
| 1977 |
Komiyama M, Breaux EJ, Bender ML. The use of cycloamylose to probe the "charge-relay" system Bioorganic Chemistry. 6: 127-136. DOI: 10.1016/0045-2068(77)90015-3 |
0.309 |
|
| 1977 |
Komiyama M, Bender ML. General base-catalyzed ester hydrolysis as a model of the "charge-relay" system Bioorganic Chemistry. 6: 13-20. DOI: 10.1016/0045-2068(77)90003-7 |
0.331 |
|
| 1976 |
Komiyama M, Bender ML. Amine-catalyzed hydrolyses of cyclodextrin cinnamates. Proceedings of the National Academy of Sciences of the United States of America. 73: 2969-72. PMID 16592347 DOI: 10.1073/Pnas.73.9.2969 |
0.385 |
|
| 1976 |
Breaux EJ, Bender ML. Direct spectrophotometric observation of an acyl-enzyme intermediate in elastase catalysis. Biochemical and Biophysical Research Communications. 70: 235-40. PMID 1275939 DOI: 10.1016/0006-291X(76)91133-5 |
0.431 |
|
| 1976 |
Kurono Y, Stamoudis V, Bender ML. The deacylation of acyl-cycloamyloses. The catalytic effects of benzimidazole derivatives on the rate Bioorganic Chemistry. 5: 393-402. DOI: 10.1016/0045-2068(76)90024-9 |
0.404 |
|
| 1975 |
Iwakura Y, Uno K, Toda F, Onozuka S, Hattori K, Bender ML. Letter: The stereochemically correct catalytic site on cyclodextrin resulting in a better enzyme model. Journal of the American Chemical Society. 97: 4432-4. PMID 1141607 DOI: 10.1021/Ja00848A068 |
0.345 |
|
| 1975 |
Means GE, Bender ML. Acetylation of human serum albumin by p-nitrophenyl acetate. Biochemistry. 14: 4989-94. PMID 241394 DOI: 10.1021/Bi00693A031 |
0.327 |
|
| 1975 |
Breaux EJ, Bender ML. The binding of specific and non-specific aldehyde substrate analogs to alpha-chymotrypsin. Febs Letters. 56: 81-4. PMID 239865 DOI: 10.1016/0014-5793(75)80116-5 |
0.305 |
|
| 1975 |
Amshey JW, Jindal SP, Bender ML. The deacylation of substituted benzol-alpha-chymotrypsins. Archives of Biochemistry and Biophysics. 169: 1-6. PMID 239634 DOI: 10.1016/0003-9861(75)90310-0 |
0.433 |
|
| 1975 |
Gruhn WB, Bender ML. Catalysis of ester hydrolysis by N-(2-dimethylaminoethyl)acetohydroxamic acid (I) Bioorganic Chemistry. 4: 219-236. DOI: 10.1016/0045-2068(75)90033-4 |
0.367 |
|
| 1975 |
Griffiths DW, Bender ML. Enhanced rates of acyl transfer to a neighboring hydroxyl group Bioorganic Chemistry. 4: 84-92. DOI: 10.1016/0045-2068(75)90028-0 |
0.353 |
|
| 1974 |
Philipp M, Bender ML. Subtilisin-catalyzed hydrolysis of peptide methyl esters. Febs Letters. 42: 282-4. PMID 4854515 DOI: 10.1016/0014-5793(74)80746-5 |
0.318 |
|
| 1974 |
Hiroara H, Bender ML, Stark RS. Acylation of alpha-chymotrypsin by oxygen and sulfur esters of specific substrates: kinetic evidence for a tetrahedral intermediate. Proceedings of the National Academy of Sciences of the United States of America. 71: 1643-7. PMID 4525454 DOI: 10.1073/Pnas.71.5.1643 |
0.356 |
|
| 1974 |
Gruhn WB, Bender ML. Enzyme models. The attachment of N-methylhydroxamic acid to cyclohexaamylose. Its reactivity and specificity with phenyl esters Bioorganic Chemistry. 3: 324-342. DOI: 10.1016/0045-2068(74)90022-4 |
0.368 |
|
| 1973 |
Philipp M, Pollack RM, Bender ML. Influence of Leaving-Group Electronic Effect on alpha-Chymotrypsin: Catalytic Constants of Specific Substrates. Proceedings of the National Academy of Sciences of the United States of America. 70: 517-20. PMID 16592059 DOI: 10.1073/Pnas.70.2.517 |
0.377 |
|
| 1973 |
Bender ML, Phillip M. Subtilisin catalysis of nonspecific anilide hydrolyses. Journal of the American Chemical Society. 95: 1665-6. PMID 4689327 DOI: 10.1021/Ja00786A054 |
0.386 |
|
| 1973 |
Griffiths DW, Bender ML. Cycloamyloses as Catalysts Advances in Catalysis. 23: 209-261. DOI: 10.1016/S0360-0564(08)60302-8 |
0.334 |
|
| 1972 |
Wedler FC, Bender ML. Evidence for the His-57 sidechain acting as a general base in the "ageing" and reactivation reactions of carbonate-inhibited -chymotrypsin. Biochemical and Biophysical Research Communications. 47: 820-3. PMID 5026298 DOI: 10.1016/0006-291X(72)90566-9 |
0.668 |
|
| 1972 |
Bender ML, Wedler FC. Phosphate and carbonate ester "aging" reactions with -chymotrypsin. Kinetics and mechanism. Journal of the American Chemical Society. 94: 2101-9. PMID 5016032 |
0.614 |
|
| 1972 |
Straub TS, Bender ML. Cycloamyloses as enzyme models. Decarboxylation of benzoylacetic acids Journal of the American Chemical Society. 94: 8881-8888. DOI: 10.1021/Ja00780A039 |
0.36 |
|
| 1972 |
Straub TS, Bender ML. Cycloamyloses as enzyme models. Decarboxylation of phenylcyanoacetate anions Journal of the American Chemical Society. 94: 8875-8881. DOI: 10.1021/Ja00780A038 |
0.36 |
|
| 1972 |
Brass HJ, Bender ML. Reactions of general bases and nucleophiles with bis(p-nitrophenyl) methylphosphonate Journal of the American Chemical Society. 94: 7421-7428. DOI: 10.1021/Ja00776A026 |
0.322 |
|
| 1972 |
Hershfield R, Bender ML. Nucleophilic and metal ion acceleration of ester hydrolysis in a hydrophobic complex. Reactive enzyme model system Journal of the American Chemical Society. 94: 1376-1377. DOI: 10.1021/Ja00759A067 |
0.327 |
|
| 1972 |
BENDER ML, WEDLER FC. ChemInform Abstract: PHOSPHAT- UND CARBONATESTER-′ALTERUNGSRK.′ MIT ALPHA-CHYMOTRYPSIN, KINETIK UND MECHANISMUS Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/chin.197224472 |
0.582 |
|
| 1971 |
Valenzuela P, Bender ML. Conformation of delta-chymotrypsin during catalysis. Chemical reactivity of the isoleucine 16 amino group in the acyl-enzyme intermediate. Biochimica Et Biophysica Acta. 235: 411-3. PMID 5317643 DOI: 10.1016/0005-2744(71)90222-1 |
0.398 |
|
| 1971 |
Valenzuela P, Bender ML. Kinetic properties of succinylated and ethylenediamine-amidated -chymotrypsins. Biochimica Et Biophysica Acta. 250: 538-48. PMID 5132914 DOI: 10.1016/0005-2744(71)90254-3 |
0.431 |
|
| 1971 |
Philipp M, Bender ML. Inhibition of serine proteases by arylboronic acids. Proceedings of the National Academy of Sciences of the United States of America. 68: 478-80. PMID 4993411 DOI: 10.1073/Pnas.68.2.478 |
0.312 |
|
| 1971 |
Hurst GH, Bender ML. Mechanisms of monofunctional and bifunctional catalysis of an ester hydrolysis. The kinetics of methyl 2,6-dicarboxybenzoate hydrolysis Journal of the American Chemical Society. 93: 704-711. DOI: 10.1021/Ja00732A025 |
0.362 |
|
| 1971 |
Congdon WI, Bender ML. The β-cyclodextrin-accelerated hydrolysis of Aryl sulfates: A model for enzymic catalysis through binding Bioorganic Chemistry. 1: 424-431. DOI: 10.1016/0045-2068(71)90044-7 |
0.371 |
|
| 1970 |
Nakagawa Y, Bender ML. Methylation of histidine-57 in alpha-chymotrypsin by methyl p-nitrobenzenesulfonate. A new approach to enzyme modification. Biochemistry. 9: 259-67. PMID 5460940 DOI: 10.1021/Bi00804A011 |
0.323 |
|
| 1970 |
Wedler FC, Killian FL, Bender ML. Reaction of acetyl-alpha-chymotrypsin and other esters with an ionizable nucleophile, monoisonitrosoacetone. Proceedings of the National Academy of Sciences of the United States of America. 65: 1120-6. PMID 5266907 |
0.657 |
|
| 1970 |
Philipp M, Polgar L, Bender ML. [12] Thiolsubtilisin (an articial enzyme) Methods in Enzymology. 19: 215-221. DOI: 10.1016/0076-6879(70)19015-X |
0.355 |
|
| 1969 |
Marshall TH, Whitaker JR, Bender ML. Porcine elastase. II. Properties of the tyrosinate-splitting enzymes and the specificity of elastase. Biochemistry. 8: 4671-7. PMID 5391861 DOI: 10.1021/Bi00840A002 |
0.316 |
|
| 1969 |
Marshall TH, Whitaker JR, Bender ML. Porcine elastase. I. The presence of tyrosinate-splitting enzymes as impurities in elastase preparations. Biochemistry. 8: 4665-71. PMID 5391860 DOI: 10.1021/Bi00840A001 |
0.367 |
|
| 1969 |
Polgár L, Bender ML. The nature of general base-general acid catalysis in serine proteases. Proceedings of the National Academy of Sciences of the United States of America. 64: 1335-42. PMID 5271756 DOI: 10.1073/Pnas.64.4.1335 |
0.333 |
|
| 1969 |
Geneste P, Bender ML. Esterolytic activity of elastase. Proceedings of the National Academy of Sciences of the United States of America. 64: 683-5. PMID 5261042 DOI: 10.1073/Pnas.64.2.683 |
0.35 |
|
| 1969 |
Valenzuela P, Bender ML. Alkaline pH dependence of delta-chymotrypsin-catalyzed hydrolysis of specific substrates. Proceedings of the National Academy of Sciences of the United States of America. 63: 1214-21. PMID 5260922 DOI: 10.1073/Pnas.63.4.1214 |
0.37 |
|
| 1969 |
Gruhn WB, Bender ML. N-methylacetohydroxamic acid catalyzed ester hydrolysis Journal of the American Chemical Society. 91: 5883-5885. DOI: 10.1021/Ja01049A038 |
0.316 |
|
| 1969 |
Wedler FC, Bender ML. pH-dependent proton absorption in chymotrypsin. Small molecule interactions Journal of the American Chemical Society. 91: 3894-3899. DOI: 10.1021/Ja01042A036 |
0.583 |
|
| 1968 |
Miller CG, Bender ML. The direct observation of an acyl-enzyme intermediate in the alpha-chymotrypsin-catalyzed hydrolysis of a specific substrate at neutral pH. Journal of the American Chemical Society. 90: 6850-2. PMID 5687712 DOI: 10.1021/Ja01026A055 |
0.42 |
|
| 1968 |
Bender ML, Marshall TH. The elastase-catalyzed hydrolysis of p-nitrophenyl trimethylacetate. Journal of the American Chemical Society. 90: 201-7. PMID 5634599 DOI: 10.1021/Ja01003A035 |
0.307 |
|
| 1967 |
Polgar L, Bender ML. The reactivity of thiol-subtilisin, an enzyme containing a synthetic functional group. Biochemistry. 6: 610-20. PMID 6047645 DOI: 10.1021/Bi00854A032 |
0.341 |
|
| 1967 |
Bender ML, Wedler FC. Ph-dependent proton absorption in chymotrypsin binding. Evidence for a ph-dependent conformation change of the enzyme. Journal of the American Chemical Society. 89: 3052-4. PMID 6043818 DOI: 10.1021/Ja00988A047 |
0.625 |
|
| 1967 |
Bender ML, Kézdy FJ, Wedler FC. Alpha-chymotrypsin: enzyme concentration and kinetics. Journal of Chemical Education. 44: 84-8. PMID 6040828 DOI: 10.1021/Ed044P84 |
0.649 |
|
| 1967 |
Brubacher LJ, Bender ML. The reaction of trans-cinnamoyl-papain with a series of polyglycinamides of varying chain length. Biochemical and Biophysical Research Communications. 27: 176-82. PMID 6035485 DOI: 10.1016/S0006-291X(67)80058-5 |
0.742 |
|
| 1967 |
Bender ML. ESTER HYDROLYSIS CATALYZED BY α -CHYMOTRYPSIN, TRYPSIN AND CYCLODEXTRINS* Transactions of the New York Academy of Sciences. 29: 301-309. DOI: 10.1111/J.2164-0947.1967.Tb02418.X |
0.346 |
|
| 1967 |
VanEtten RL, Clowes GA, Sebastian JF, Bender ML. The mechanism of the cycloamylose-accelerated cleavage of phenyl esters Journal of the American Chemical Society. 89: 3253-3262. DOI: 10.1021/Ja00989A028 |
0.316 |
|
| 1967 |
VanEtten RL, Sebastian JF, Clowes GA, Bender ML. Acceleration of phenyl ester cleavage by cycloamyloses. A model for enzymic specificity Journal of the American Chemical Society. 89: 3242-3253. DOI: 10.1021/Ja00989A027 |
0.378 |
|
| 1967 |
Bender ML, Heck Hd. Carbonyl Oxygen Exchange in General Base Catalyzed Ester Hydrolysis Journal of the American Chemical Society. 89: 1211-1220. DOI: 10.1021/Ja00981A030 |
0.315 |
|
| 1966 |
Bender ML, Begué-Cantón ML, Blakeley RL, Brubacher LJ, Feder J, Gunter CR, Kézdy FJ, Killheffer JV, Marshall TH, Miller CG, Roeske RW, Stoops JK. The determination of the concentration of hydrolytic enzyme solutions: alpha-chymotrypsin, trypsin, papain, elastase, subtilisin, and acetylcholinesterase. Journal of the American Chemical Society. 88: 5890-913. PMID 5980876 |
0.742 |
|
| 1966 |
Brubacher LJ, Bender ML. The preparation and properties of trans-cinnamoyl-papain. Journal of the American Chemical Society. 88: 5871-80. PMID 5980875 DOI: 10.1021/Ja00976A032 |
0.725 |
|
| 1966 |
Whitaker JR, Menger F, Bender ML. The kinetics of some carboxypeptidase A and acetylcarboxypeptidase A catalyzed hydrolyses. Biochemistry. 5: 386-92. PMID 5938953 DOI: 10.1021/Bi00865A048 |
0.59 |
|
| 1966 |
Bender ML, Brubacher LJ. The Kinetics and Mechanism of Papain-Catalyzed Hydrolyses1 Journal of the American Chemical Society. 88: 5880-5889. DOI: 10.1021/Ja00976A033 |
0.765 |
|
| 1966 |
Polgar L, Bender ML. A New Enzyme Containing a Synthetically Formed Active Site. Thiol-Subtilisin1 Journal of the American Chemical Society. 88: 3153-3154. DOI: 10.1021/Ja00965A060 |
0.339 |
|
| 1966 |
Williams A, Bender ML. Studies on the Mechanism of Oxime and Ketimine Formation1 Journal of the American Chemical Society. 88: 2508-2513. DOI: 10.1021/Ja00963A027 |
0.425 |
|
| 1966 |
Bender ML, Williams A. Ketimine Intermediates in Amine-Catalyzed Enolization of Acetone1a Journal of the American Chemical Society. 88: 2502-2508. DOI: 10.1021/Ja00963A026 |
0.524 |
|
| 1966 |
Bender ML, Van Etten R, Clowes GA. The Mechanism of the Cycloamylose-Catalyzed Reactions of Phenyl Esters. A Model for Journal of the American Chemical Society. 88: 2319-2320. DOI: 10.1021/Ja00962A044 |
0.382 |
|
| 1965 |
BENDER ML, WHITAKER JR, MENGER F. THE EFFECT OF ENZYME ACETYLATION ON THE KINETICS OF THE CARBOXYPERTIDASE-A-CATALYZED HYDROLYSIS OF HIPPURL-L-BETA-PHENYLLACTIC ACID. Proceedings of the National Academy of Sciences of the United States of America. 53: 711-6. PMID 14324526 DOI: 10.1073/Pnas.53.4.711 |
0.569 |
|
| 1965 |
KEZDY FJ, BENDER ML. THE ACYL-ENZYME DIMER OF CHYMOTRYPISM. Biochemistry. 4: 104-13. PMID 14285226 DOI: 10.1021/Bi00877A018 |
0.37 |
|
| 1965 |
Bender ML, Kézdy FJ, Feder J. Transient formation of an inactive intermediate in the reaction with alpha-N-benzoyl-L-arginine ethyl ester and alpha-N-benzoyl-L-arginine. Journal of the American Chemical Society. 87: 4955-7. PMID 5844469 DOI: 10.1021/Ja00949A050 |
0.303 |
|
| 1965 |
Bender ML, Kézdy FJ. The trypsin-catalyzed hydrolysis of the p-nitrophenyl, methyl, and benzyl esters of alpha-N-benzyloxycarbonyl-L-lysine. Journal of the American Chemical Society. 87: 4954-5. PMID 5844468 DOI: 10.1021/Ja00949A049 |
0.32 |
|
| 1965 |
Bender ML, Kézdy FJ, Feder J. The kinetics of the trypsin-catalyzed hydrolysis of p-nitrophenyl alpha-N-benzyloxycarbonyl-L-lysinate hydrochloride. Journal of the American Chemical Society. 87: 4953-4. PMID 5844467 DOI: 10.1021/Ja00949A048 |
0.329 |
|
| 1965 |
Bender ML, Reinstein JA, Silver MS, Mikulak R. Kinetics and Mechanism of the Hydroxide Ion and Morpholine-Catalyzed Hydrolysis of Methyl o-Formylbenzoate. Participation by the Neighboring Aldehyde Group1 Journal of the American Chemical Society. 87: 4545-4553. DOI: 10.1021/Ja00948A026 |
0.313 |
|
| 1964 |
Bender ML, Brubacher LJ. The Acyl-enzyme Intermediate,trans-Cinnamoylpapain Journal of the American Chemical Society. 86: 5333-5334. DOI: 10.1021/Ja01077A058 |
0.771 |
|
| 1964 |
Bender ML, Killheffer JV, Kezdy FJ. An Identity of the Rates of Deacylation of Nonionic Acyl-α-chymotrypsins and Acyl-trypsins Journal of the American Chemical Society. 86: 5330-5331. DOI: 10.1021/Ja01077A056 |
0.301 |
|
| 1964 |
Bender ML, Clement GE, Gunter CR, Kezdy FJ. The Kinetics of α-Chymotrypsin Reactions in the Presence of Added Nucleophiles Journal of the American Chemical Society. 86: 3697-3703. DOI: 10.1021/Ja01072A019 |
0.338 |
|
| 1964 |
Kezdy FJ, Clement GE, Bender ML. The Observation of Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Reactions of N-Acetyl-L-tryptophan Derivatives at Low pH Journal of the American Chemical Society. 86: 3690-3696. DOI: 10.1021/Ja01072A018 |
0.422 |
|
| 1964 |
Bender ML, Clement GE, Kezdy FJ, Heck HD. The Correlation of the pH (pD) Dependence and the Stepwise Mechanism of α-Chymotrypsin-Catalyzed Reactions Journal of the American Chemical Society. 86: 3680-3690. DOI: 10.1021/Ja01072A017 |
0.331 |
|
| 1964 |
Zerner B, Bond RPM, Bender ML. Kinetic Evidence for the Formation of Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Hydrolyses of Specific Substrates Journal of the American Chemical Society. 86: 3674-3679. DOI: 10.1021/Ja01072A016 |
0.425 |
|
| 1964 |
Zerner B, Bender ML. The Kinetic Consequences of the Acyl-Enzyme Mechanism for the Reactions of Specific Substrates with Chymotrypsin Journal of the American Chemical Society. 86: 3669-3674. DOI: 10.1021/Ja01072A015 |
0.436 |
|
| 1964 |
Kezdy FJ, Bender ML. The Observation of Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Hydrolysis of Specific Ester Substrates at Low pH Journal of the American Chemical Society. 86: 937-938. DOI: 10.1021/Ja01059A048 |
0.427 |
|
| 1963 |
Bender ML, Kezdy FJ, Zerner B. Intramolecular Catalysis in the Hydrolysis ofp-Nitrophenyl Salicylates Journal of the American Chemical Society. 85: 3017-3024. DOI: 10.1021/Ja00902A032 |
0.434 |
|
| 1963 |
Bender ML, Lawlor JM. Isotopic and Kinetic Studies of the Mechanism of Hydrolysis of Salicyl Phosphate. Intramolecular General Acid Catalysis Journal of the American Chemical Society. 85: 3010-3017. DOI: 10.1021/Ja00902A031 |
0.38 |
|
| 1963 |
Bender ML, Silver MS. The Hydrolysis of Substituted 2-Phenyl-1,3-dioxanes Journal of the American Chemical Society. 85: 3006-3010. DOI: 10.1021/Ja00902A030 |
0.347 |
|
| 1963 |
Bender ML, Clement GE, Kezdy FJ, Zerner B. Sigmoid and Bell-Shaped pH-Rate Profiles in α-Chymotrypsin-Catalyzed Hydrolyses. a Mechanistic Correlation Journal of the American Chemical Society. 85: 358-359. DOI: 10.1021/Ja00886A033 |
0.316 |
|
| 1963 |
Zerner B, Bender ML. Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Hydrolysis of “Specific” Substrates. the Relative Rates of Hydrolysis of Ethyl, Methyl andp-Nitrophenyl Esters of N-Acetyl-L-Tryptophan Journal of the American Chemical Society. 85: 356-358. DOI: 10.1021/Ja00886A031 |
0.403 |
|
| 1963 |
Bender ML, Chen MC. Acylium Ion Formation in the Reactions of Carboxylic Acid Derivatives. IV. The Acid-catalyzed Hydrolysis of Methyl 4-Substituted-2,6-dimethylbenzoates Journal of the American Chemical Society. 85: 37-40. DOI: 10.1021/Ja00884A007 |
0.357 |
|
| 1963 |
Bender ML, Chen MC. Acylium Ion Formation in the Reactions of Carboxylic Acid Derivatives. III. The Hydrolysis of 4-Substituted-2,6-dimethylbenzoyl Chlorides Journal of the American Chemical Society. 85: 30-36. DOI: 10.1021/Ja00884A006 |
0.344 |
|
| 1962 |
KEZDY FJ, BENDER ML. The kinetics of the alpha-chymotrypsin-catalyzed hydrolysis of p-nitrophenyl acetate. Biochemistry. 1: 1097-106. PMID 14032227 DOI: 10.1021/Bi00912A021 |
0.355 |
|
| 1962 |
Bender ML, Jones JM. Nucleophilic Reactions of Morpholine with the Benzoyl Halides. The Presence of an Element Effect1 The Journal of Organic Chemistry. 27: 3771-3774. DOI: 10.1021/Jo01058A006 |
0.314 |
|
| 1962 |
Westheimer FH, Bender ML. Imidazole Catalysis of the Hydrolysis of δ-Thiovalerolactone Journal of the American Chemical Society. 84: 4908-4909. DOI: 10.1021/Ja00883A055 |
0.704 |
|
| 1962 |
Bender ML, Silver MS. The Hydrolysis of Methylo-Formylbenzoate. Participation of the Neighboring Aldehyde Group in the Hydroxide Ion and Morpholine-Catalyzed Reactions Journal of the American Chemical Society. 84: 4589-4590. DOI: 10.1021/Ja00882A042 |
0.33 |
|
| 1962 |
Bender ML. The Mechanism of α-Chymotrypsin-catalyzed Hydrolyses1-3 Journal of the American Chemical Society. 84: 2582-2590. DOI: 10.1021/Ja00872A024 |
0.32 |
|
| 1962 |
Bender ML, Nakamura K. The Effect of Structure on the Rates of Some α-Chymotrypsin-catalyzed Reactions Journal of the American Chemical Society. 84: 2577-2582. DOI: 10.1021/Ja00872A023 |
0.345 |
|
| 1962 |
Bender ML, Hamilton GA. Kinetic Isotope Effects of Deuterium Oxide on Several α-Chymotrypsin-catalyzed Reactions Journal of the American Chemical Society. 84: 2570-2576. DOI: 10.1021/Ja00872A022 |
0.391 |
|
| 1962 |
Bender ML, Schonbaum GR, Zerner B. ThepH Dependence of Some α-Chymotrypsin-catalyzed Hydrolyses1-3 Journal of the American Chemical Society. 84: 2562-2570. DOI: 10.1021/Ja00872A021 |
0.303 |
|
| 1962 |
Bender ML, Kaiser ET. The Mechanism of Trypsin-catalyzed Hydrolyses. The Cinnamoyl-trypsin Intermediate1-3 Journal of the American Chemical Society. 84: 2556-2561. DOI: 10.1021/Ja00872A020 |
0.37 |
|
| 1962 |
Bender ML, Zerner B. The Formation of an Acyl-enzyme Intermediate in the α-Chymotrypsin-catalyzed Hydrolyses of Non-labiletrans-Cinnamic Acid Esters1-3 Journal of the American Chemical Society. 84: 2550-2555. DOI: 10.1021/Ja00872A019 |
0.41 |
|
| 1962 |
Bender ML, Schonbaum GR, Zerner B. Spectrophotometric Investigations of the Mechanism of α-Chymotrypsin-catalyzed Hydrolyses. Detection of the Acyl-enzyme Intermediate1-3 Journal of the American Chemical Society. 84: 2540-2550. DOI: 10.1021/Ja00872A018 |
0.393 |
|
| 1962 |
Bender ML, Connors KA. A Non-enzymatic Olefinic Hydration under Neutral Conditions: the Kinetics and Mechanism of the Hydration of Fumaric Acid Monoanion Journal of the American Chemical Society. 84: 1980-1986. DOI: 10.1021/Ja00869A041 |
0.32 |
|
| 1962 |
Bender ML, Pollock EJ, Neveu MC. Deuterium Oxide Solvent Isotope Effects in the Nucleophilic Reactions of Phenyl Esters Journal of the American Chemical Society. 84: 595-599. DOI: 10.1021/Ja00863A019 |
0.326 |
|
| 1961 |
Bender ML, Kaiser ET, Zerner B. A COMPARISON OF THE ACYL-ENZYME INTERMEDIATES, CINNAMOYL-TRYPSIN AND CINNAMOYL-α-CHYMOTRYPSIN1 Journal of the American Chemical Society. 83: 4656-4657. DOI: 10.1021/Ja01483A036 |
0.389 |
|
| 1961 |
Bender ML, Matsui H, Thomas RJ, Tobey SW. The Concurrent Alkaline Hydrolysis and Isotopic Oxygen Exchange of Several Alkyl Benzoates and Lactones1,2 Journal of the American Chemical Society. 83: 4193-4196. DOI: 10.1021/Ja01481A023 |
0.306 |
|
| 1961 |
Bender ML, Thomas RJ. The Concurrent Alkaline Hydrolysis and Isotopic Oxygen Exchange of a Series of p-Substituted Methyl Benzoates1,2 Journal of the American Chemical Society. 83: 4189-4193. DOI: 10.1021/Ja01481A022 |
0.311 |
|
| 1961 |
Bender ML, Thomas RJ. The Concurrent Alkaline Hydrolysis and Isotopic Oxygen Exchange of a Series of p-Substituted Acetanilides1,2 Journal of the American Chemical Society. 83: 4183-4189. DOI: 10.1021/Ja01481A021 |
0.318 |
|
| 1961 |
Bender ML, Connors KA. A NON-ENZYMATIC OLEFINIC HYDRATION UNDER NEUTRAL CONDITIONS. THE KINETICS OF THE HYDRATION OF FUMARIC ACID MONOANION Journal of the American Chemical Society. 83: 4099-4100. DOI: 10.1021/Ja01480A038 |
0.302 |
|
| 1961 |
Bender ML, Zerner B. THE FORMATION OF THE ACYL-ENZYME INTERMEDIATE, TRANS-CINNAMOYL-α-CHYMOTRYPSIN, IN THE HYDROLYSES OF NON-LABILE TRANS-CINNAMIC ACID ESTERS1,2 Journal of the American Chemical Society. 83: 2391-2392. DOI: 10.1021/Ja01471A040 |
0.398 |
|
| 1961 |
Bender ML, Schonbaum GR, Hamilton GA, Zerner B. THE INFLUENCE OF pH AND DEUTERIUM OXIDE ON THE KINETICS OF α-CHYMOTRYPSIN-CATALYZED REACTIONS1,2 Journal of the American Chemical Society. 83: 1255-1256. DOI: 10.1021/Ja01466A059 |
0.326 |
|
| 1961 |
Bender ML, Ladenheim H, Chen MC. Acylium Ion Formation in the Reactions of Carboxylic Acid Derivatives. II. The Hydrolysis and Oxygen Exchange of Methyl Mesitoate in Sulfuric Acid1a Journal of the American Chemical Society. 83: 123-127. DOI: 10.1021/Ja01462A024 |
0.334 |
|
| 1960 |
Bender ML, Feng MS. Secondary Deuterium Isotope Effects in the Reactions of Carboxylic Acid Derivatives1a Journal of the American Chemical Society. 82: 6318-6321. DOI: 10.1021/Ja01509A032 |
0.303 |
|
| 1960 |
Bender ML, Glasson WA. The Kinetics of the α-Chymotrypsin-catalyzed Hydrolysis and Methanolysis of Acetyl-L-phenylalanine Methyl Ester. Evidence for the Specific Binding of Water on the Enzyme Surface1 Journal of the American Chemical Society. 82: 3336-3342. DOI: 10.1021/Ja01498A027 |
0.375 |
|
| 1960 |
Ladenheim H, Bender ML. Acylium Ion Formation in the Reactions of Carboxylic Acid Derivatives. I. Application of the HRAcidity Function to the Diazotization of Benzamide in Sulfuric Acid1 Journal of the American Chemical Society. 82: 1895-1900. DOI: 10.1021/Ja01493A016 |
0.311 |
|
| 1960 |
Bender ML. Mechanisms of Catalysis of Nucleophilic Reactions of Carboxylic Acid Derivatives. Chemical Reviews. 60: 53-113. DOI: 10.1021/Cr60203A005 |
0.379 |
|
| 1959 |
Schonbaum GR, Nakamura K, Bender ML. DIRECT SPECTROPHOTOMETRIC EVIDENCE FOR AN ACYL-ENZYME INTERMEDIATE IN THE CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF O-NITROPHENYL CINNAMATE1 Journal of the American Chemical Society. 81: 4746-4747. DOI: 10.1021/Ja01526A076 |
0.373 |
|
| 1959 |
Bender ML, Chow Y. Electrostatic Catalysis. The Reactivity of an Ester and a Nucleophile of Opposite Charge1a Journal of the American Chemical Society. 81: 3929-3933. DOI: 10.1021/Ja01524A030 |
0.368 |
|
| 1958 |
Bender ML, Neveu MC. Intramolecular Catalysis of Hydrolytic Reactions. IV. A Comparison of Intramolecular and Intermolecular Catalysis1,2 Journal of the American Chemical Society. 80: 5388-5391. DOI: 10.1021/Ja01553A017 |
0.361 |
|
| 1958 |
Bender ML, Chloupek F, Neveu MC. Intramolecular Catalysis of Hydrolytic Reactions. III. Intramolecular Catalysis by Carboxylate Ion in the Hydrolysis of Methyl Hydrogen Phthalate1,2 Journal of the American Chemical Society. 80: 5384-5387. DOI: 10.1021/Ja01553A016 |
0.341 |
|
| 1958 |
Bender ML, Chow Y, Chloupek F. Intramolecular Catalysis of Hydrolytic Reactions. II. The Hydrolysis of Phthalamic Acid1,2 Journal of the American Chemical Society. 80: 5380-5384. DOI: 10.1021/Ja01553A015 |
0.355 |
|
| 1958 |
Buist GJ, Bender ML. Carbon-14 Kinetic Isotope Effects. IV. The Effect of Activation Energy on Some Carbon-14 Kinetic Isotope Effects1,2 Journal of the American Chemical Society. 80: 4308-4311. DOI: 10.1021/Ja01549A048 |
0.321 |
|
| 1958 |
Bender ML, Buist GJ. Carbon-14 Kinetic Isotope Effects. III.1,2The Hydrolysis of 2-Chloro-2-methylpropane-2-C14 Journal of the American Chemical Society. 80: 4304-4307. DOI: 10.1021/Ja01549A047 |
0.361 |
|
| 1957 |
Bender ML, Hoeg DF. Carbon-14 Kinetic Isotope Effects in Nucleophilic Substitution Reactions1 Journal of the American Chemical Society. 79: 5649-5654. DOI: 10.1021/Ja01578A017 |
0.336 |
|
| 1957 |
Bender ML, Turnquest BW. The Kinetics and Oxygen Exchange of the Cupric Ion-catalyzed Hydrolysis of α-Amino Esters1 Journal of the American Chemical Society. 79: 1889-1893. DOI: 10.1021/Ja01565A033 |
0.327 |
|
| 1957 |
Bender ML, Turnquest BW. General Basic Catalysis of Ester Hydrolysis and Its Relationship to Enzymatic Hydrolysis1 Journal of the American Chemical Society. 79: 1656-1662. DOI: 10.1021/Ja01564A035 |
0.331 |
|
| 1957 |
Bender ML, Turnquest BW. The Imidazole-catalyzed Hydrolysis of p-Nitrophenyl Acetate1 Journal of the American Chemical Society. 79: 1652-1655. DOI: 10.1021/Ja01564A034 |
0.311 |
|
| 1957 |
Bender ML, Kemp KC. The Kinetics of the α-Chymotrypsin-catalyzed Oxygen Exchange of Carboxylic Acids1 Journal of the American Chemical Society. 79: 116-120. DOI: 10.1021/Ja01558A030 |
0.328 |
|
| 1957 |
Bender ML, Kemp KC. Oxygen-18 Studies of the Mechanism of the α-Chymotrypsin-catalyzed Hydrolysis of Esters1 Journal of the American Chemical Society. 79: 111-116. DOI: 10.1021/Ja01558A029 |
0.323 |
|
| 1956 |
Bender ML, Robbins H. The Reactions of Silver Nitrate with Some Substituted Neopentyl Bromides Journal of the American Chemical Society. 78: 1699-1702. DOI: 10.1021/Ja01589A059 |
0.346 |
|
| 1955 |
Bender ML, Turnquest BW. The Acidic, Basic and α-Chymotrypsin-catalyzed Hydrolyses of Some Esters. A Kinetic Comparison1 Journal of the American Chemical Society. 77: 4271-4275. DOI: 10.1021/Ja01621A032 |
0.364 |
|
| 1955 |
Bender ML, Ginger RD. Intermediates in the Reactions of Carboxylic Acid Derivatives. IV. The Hydrolysis of Benzamide1-3 Journal of the American Chemical Society. 77: 348-351. DOI: 10.1021/Ja01607A032 |
0.374 |
|
| 1953 |
Bender ML. Intermediates in the Reactions of Carboxylic Acid Derivatives. II. Infrared Absorption Spectra as Evidence for the Formation of Addition Compounds of Carboxylic Acid Derivatives1,2 Journal of the American Chemical Society. 75: 5986-5990. DOI: 10.1021/Ja01119A063 |
0.308 |
|
| 1949 |
Hass HB, Janet Berry E, Bender ML. Carbon aralkylations of nitro paraffins Journal of the American Chemical Society. 71: 2290-2291. DOI: 10.1021/Ja01175A005 |
0.549 |
|
| 1949 |
Hass HB, Bender ML. The reaction of benzyl halides with the sodium salt of 2-nitropropane. A general synthesis of substituted benzaldehydes Journal of the American Chemical Society. 71: 1767-1769. DOI: 10.1021/Ja01173A066 |
0.625 |
|
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