Quantitative Structure Activity Relationship (71 results)

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Taschenbuch. Condition: Neu. QSAR Modeling on Some Anti-Diabetic Analogs | Quantitative Structure Activity Relationship (QSAR) Studies of Some Antidiabetic Analogs | Vaijinath A. Verma | Taschenbuch | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9786200505040 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

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Condition: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | Diabetes mellitus is a disease in which the body is unable to produce or unable to properly use and store glucose (a form of sugar). Glucose backs up in the bloodstream causing ones blood glucose or "sugar" to raise too high. The diabetes Mellitus having their own historical aspect in 1552 B.C. earliest known of diabetes mentioned on 3rd dynasty Egyptian papyrus by physician mention polyuria (frequent Urination) as a symptom. It has some important landmarks as 1869, German medical student Pual Langerhance discovered that pancreas contains two distinct groups of cells-Acinar cells and islets (cells that are clustered in islands). Quantitative Structure Activity Relationship (QSAR) studies represent the non-experimental part of drug design, including investigation of both structure-activity and structure-property relationship. This is an intellectual exercise comprising assembling, manipulating and inspecting information got from physical, chemical and biological experiments and correlating these to biological activity.…

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Gebundene Ausgabe. Condition: Neu. The book, which is related to QSAR in sciences, is divided into five main chapters. The first chapter is the Introductory chapter. The second chapter aims to provide an update of the recent advances in the field of rational design of PDE inhibitors. The third chapter includes designing a series of peptidic inhibitors that possessed a substrate transition-state analog and evaluating the structure-activity relationship of the designed inhibitors, based on docking and scoring, using the docking simulation software Molecular Operating Environment. The aim of the forth chapter is to develop structure-property relationships for the qualitative and quantitative prediction of the reverse-phase liquid chromatographic retention times of chlorogenic acids. The final chapter aims to determine the model of interactions between the natural compounds with anti-inflammatory molecular target by molecular docking analysis. Sprache: Englisch Gewicht in Gramm: 347.…

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