QSAR Analysis of the Subtilisin Hydrolysis of X-Phenyl Hippurates
Author:
Publisher
Wiley
Subject
Pharmacology
Reference20 articles.
1. The use of crystallography, graphics, and quantitative structure-activity relationships in the analysis of the papain hydrolysis of X-phenyl hippurates
2. A Comparison by QSAR, Crystallography, and Computer Graphics of the Inhibition of Various Dihydrofolate Reductases by 5-(X-Benzyl)-2,4-diamino-pyrimidines
3. Crystallography, quantitative structure-activity relationships, (QSAR) and molecular graphics in a comparative analysis of the inhibition of dihydrofolate reductase from chicken liver and Lactobacillus casei by 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(substituted-phenyl)-s-triazines
4. Papain hydrolysis of X-phenyl-N-methanesulfonyl glycinates: A quantitative structure-activity relationship and molecular graphics analysis
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2. Azapeptides as Inhibitors and Active Site Titrants for Cysteine Proteinases;Journal of Medicinal Chemistry;1998-03-20
3. Comparative QSAR: Toward a Deeper Understanding of Chemicobiological Interactions;Chemical Reviews;1996-01-01
4. Descriptors and Techniques for Quantitative Structure –Biodegradability Studies;SAR and QSAR in Environmental Research;1996-01
5. QSAR analysis of the subtilisin hydrolysis of X-phenyl hippurates. II. A study of subtilisin BPN′;Chemico-Biological Interactions;1988
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