Separation of polar, steric and specific effects in the α-chymotrypsin-catalyzed hydrolysis of acyl-substituted p-nitrophenyl esters
- 23 October 1970
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 41 (2) , 464-470
- https://doi.org/10.1016/0006-291x(70)90528-0
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Deacylation rates of several trifluoromethyl-substituted acylchymotrypsinsBiochemistry, 1969
- Steric effects in the acylation of α-chymotrypsinBiochemistry, 1969
- Steric Effects in the Deacylation of Acyl-Chymotrypsins*Biochemistry, 1967
- The Determination of the Concentration of Hydrolytic Enzyme Solutions: α-Chymotrypsin, Trypsin, Papain, Elastase, Subtilisin, and Acetylcholinesterase1Journal of the American Chemical Society, 1966
- An Electrophilic Mechanism in the Chymotrypsin-Catalyzed Hydrolysis of Anilide Substrates1Journal of the American Chemical Society, 1965
- The Effect of Substituents on the Deacylation of Benzoyl-ChymotrypsinsBiochemistry, 1962
- The Effect of Structure on the Rates of Some α-Chymotrypsin-catalyzed ReactionsJournal of the American Chemical Society, 1962
- A Method of Synthesis of Long Peptide Chains Using a Synthesis of Oxytocin as an ExampleJournal of the American Chemical Society, 1959
- ACYLATION OF THE ENZYMATIC SITE OF δ-CHYMOTRYPSIN BY ESTERS, ACID ANHYDRIDES, AND ACID CHLORIDESPublished by Elsevier ,1957
- The molecular weight of a-chymotrypsinogenBiochimica et Biophysica Acta, 1957