The steric effect of the leaving group in the α-chymotrypsin-catalyzed hydrolysis of acetyl-l-phenylalanine p-alkoxycarbonyl anilides
- 1 September 1980
- journal article
- research article
- Published by Elsevier in Bioorganic Chemistry
- Vol. 9 (3) , 318-324
- https://doi.org/10.1016/0045-2068(80)90042-5
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Catalysis and leaving group binding in anilide hydrolysis by chymotrypsinBiochimica et Biophysica Acta (BBA) - Enzymology, 1978
- Detection of a tetrahedral intermediate in the trypsin-catalysed hydrolysis of specific ring-activated anilidesBiochimica et Biophysica Acta (BBA) - Enzymology, 1978
- Stereoelectronic Control in Hydrolytic ReactionsHETEROCYCLES, 1977
- Enthalpy-entropy compensation. 2. Separation of the chemical from the statistical effectThe Journal of Physical Chemistry, 1976
- Enthalpy-entropy compensation. 1. Some fundamental statistical problems associated with the analysis of van't Hoff and Arrhenius dataThe Journal of Physical Chemistry, 1976
- Structure‐Activity Relationship in the Urokinase Hydrolysis of α‐N‐Acetyl‐l‐lysine AnilidesEuropean Journal of Biochemistry, 1975
- Leaving group specificity in the chymotrypsin-catalyzed hydrolysis of peptides. Stereochemical interpretationBiochemistry, 1973
- Chymotrypsinogen family of proteins. XVI. Enthalpy-entropy compensation phenomenon of .alpha.-chymotrypsin and the temperature of minimum sensitivityThe Journal of Physical Chemistry, 1971
- Chymotrypsin catalysis. Evidence for a new intermediateJournal of the American Chemical Society, 1969
- The Relative Rates of Alcoholysis of Certain Aralkyl p-NitrobenzoatesJournal of the American Chemical Society, 1939