On the Active Site of α-Chymotrypsin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference27 articles.
1. Action of α-Chymotrypsin on the Diethyl Esters of Fumaric, Maleic, and Acetylenedicarboxylic Acids1
2. Association of Substrates with α-Chymotrypsin, Diethyl α-Acetoxysuccinate, and Diethyl Malate1
3. The Mode of Action of the Crystalline Pancreatic Proteolytic Enzymes.
4. AN INTERPRETATION OF THE KINETIC BEHAVIOR OF MODEL SUBSTRATES OF -CHYMOTRYPSIN
5. THE ACTIVE SITE IN -CHYMOTRYPSIN: METHYL 3,4-DIHYDROISOCOUMARIN-3-CARBOXYLATE I
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2. NH2 As a Directing Group: From the Cyclopalladation of Amino Esters to the Preparation of Benzolactams by Palladium(II)-Catalyzed Carbonylation of N-Unprotected Arylethylamines;Organometallics;2013-01-10
3. Isoquinoline Carboxylic Acids and Their Hydrogenated Derivatives;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
4. Probing the Active Sites of Enzymes with Conformationally Restricted Substrate Analogs;Progress in Physical Organic Chemistry;2007-04-04
5. Preferred hydrolysis of methyl d-pyroglutamates (5-carbomethoxy-2-pyrrolidones) by α-chymotrypsin;Bioorganic Chemistry;1977-09
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