Steric Enhancement of Imidazole Basicity incis-Urocanic Acid Derivatives: Models for the Action of Chymotrypsin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
Reference18 articles.
1. A New Concept for the Mechanism of Action of Chymotrypsin: The Role of the Low-Barrier Hydrogen Bond
2. A Low-Barrier Hydrogen Bond in the Catalytic Triad of Serine Proteases
3. The role of short hydrogen bonds in mechanisms of enzymatic action
4. Efficient Synthesis ofN-Triphenylmethyl α-Amino Acids
5. A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization
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2. Glycosylated Liposomes with Proton Sponge Capacity: Novel Hepatocyte- Specific Gene Carriers;Current Drug Delivery;2013-11
3. On the Role of Short and Strong Hydrogen Bonds on the Mechanism of Action of a Model Chymotrypsine Active Site;The Journal of Physical Chemistry A;2009-04-22
4. Determination of the Dissociation Constants of Urocanic Acid Isomers in Aqueous Solutions;Monatshefte für Chemie - Chemical Monthly;2007-08-13
5. Steric and aromatic impact on intramolecular hydrogen bonds ino-hydroxyaryl ketones and ketimines;Journal of Physical Organic Chemistry;2005-10
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