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state-of-the-art in their field of investigation and provide their views and perspectives for future research Chapters are extensively;
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This book provides basic and applied knowledge about monoamine oxidase inhibitors (MAOIs), their classification, and clinical application;
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then given, in turn, of the main non-depot antipsychotic drugs, antipsychotic depot injections, antimanic drugs, tricyclic and related;
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determination and even interactive presentation on the web. Methods driving the latest automated structure determination pipelines are explained, as;
Vergelijkbare producten zoals Advancing Methods for Biomolecular Crystallography
determination and even interactive presentation on the web. Methods driving the latest automated structure determination pipelines are explained, as;
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Family of Oxidases, Vanillyl alcohol oxidase, Choline oxidases, Aryl alcohol oxidase, D- and L-amino acid oxidases, Sugar oxidases, Phenolic;
Vergelijkbare producten zoals Flavin-Dependent Enzymes: Mechanisms, Structures and Applications
monooxygenases, monoamine oxidases and other amine oxidases, aldehyde oxidase and xanthine dehydrogenase, peroxidases, and dehydrogenases-reductases;
Vergelijkbare producten zoals The Biochemistry of Drug Metabolism: Volume 1: Principles, Redox Reactions, Hydrolyses
amine oxidases also focuses attention on their catalytic mechanism, as these enzymes have been studied in greater depth.As the presentation;
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and oxygenases. Multi-copper oxidases are an important class of oxidases reducing dioxygen in a four-electron reduction to water with;
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drawbacks of the benzodiazepines, namely their potential for tolerance and dependency, there has been a renewed interest in alternative anxiolytics;
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Focusing on the development of enzyme inhibitors as therapeutic drugs, Enzymes and Their Inhibitors: Drug Development provides a concise;
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new information on proteases, oxidases, polyphenol oxidases, lipoxygenases and the enzymology of biotechnology.;
Vergelijkbare producten zoals Principles of Enzymology for the Food Sciences
Focusing on the development of enzyme inhibitors as therapeutic drugs, Enzymes and Their Inhibitors: Drug Development provides a concise;
Vergelijkbare producten zoals Enzymes and Their Inhibitors: Drug Development
encountered and their control methods, environmental factors affecting inhibition, material selection strategies, and economic aspects of corrosion;
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(PDE) inhibitors, this book focuses on new and emerging PDE targets and their inhibitors. Drug development options for all major human PDE;
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neurological and neuropsychiatric diseases, the levels of trace amines are unusually high with an imbalance in their functions. Furthermore, the;
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inhibitors and their clinical applications, as well as future prospects for their use. Up-to-date summary of biochemistry and pharmacology;
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> Provides a structural correlation of third and fourth generation EGFR inhibitors, reviewing both their design strategies and typical;
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Viral Proteases and Their Inhibitors provides a thorough examination of viral proteases from their molecular components, to therapeutic;
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of these enzymes and their misregulation has been shown to be involved in the onset and progression of many diseases including cancer and;
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of these enzymes and their misregulation has been shown to be involved in the onset and progression of many diseases including cancer and;
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century has seen the emergence of targeted therapy, resulting from the identification of molecular pathways in cells and their alterations;
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side effects. Beginning with a discussion of the huge potential of a -glucosidase inhibitor leads and adaptations, and highlighting their;
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protease inhibitors five have been marketed during 1995-1999. They are saquinavir, ritonavir, indinavir, nelfinavir and ampre- navir. Their;
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development in a number of ways, including suppression of oxygen radicals, oncogenes, and metastases. Epidemiologic evidence supports their prevention;
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The first thorough review of cyclooxygenase inhibitors, including their toxicity mechanisms and toxicopathological risks Cyclooxygenases;
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classification of HDAC inhibitors based on their structural attributes, and addresses HDAC-induced cytotoxicity.. Lastly, it discusses and;
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