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Titlebook: Enzyme Kinetics in Drug Metabolism; Fundamentals and App Swati Nagar,Upendra A. Argikar,Donald Tweedie Book 2021Latest edition Springer Sci

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發(fā)表于 2025-3-21 19:23:12 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Enzyme Kinetics in Drug Metabolism
副標(biāo)題Fundamentals and App
編輯Swati Nagar,Upendra A. Argikar,Donald Tweedie
視頻videohttp://file.papertrans.cn/314/313090/313090.mp4
概述Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Enzyme Kinetics in Drug Metabolism; Fundamentals and App Swati Nagar,Upendra A. Argikar,Donald Tweedie Book 2021Latest edition Springer Sci
描述.This second edition further develops the principles of applying kinetic principles to drug metabolizing enzymes and transporters. Chapters are divided into six sections detailing fundamental principles of enzyme kinetics, enzyme and transporter structures, highlighting specific oxidative and conjugative drug metabolizing enzymes and drug transporters, modeling approaches for drug metabolizing enzymes and transporters, understanding of variability both experimental and interindividual (pharmacogenomic), and expanded case studies that provide real life examples of applying these principles.?Written in the highly successful?.Methods in Molecular Biology?.series format, chapters include introductions to their respective topics, in some cases step-by-step instructions with readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls with extensive cross referencing to assist in learning.? ..?..Authoritativeand fully updated,?.Enzyme Kinetics in Drug Metabolism: Fundamentals and Applications, Second Edition.?serves as a practical teaching tool for novice and advanced scientists interested in the fundamental concepts..
出版日期Book 2021Latest edition
關(guān)鍵詞Kinetic models; Drug-drug interactions; Drug metabolizing enzymes; Regulatory guidelines; Drug transport
版次2
doihttps://doi.org/10.1007/978-1-0716-1554-6
isbn_softcover978-1-0716-1556-0
isbn_ebook978-1-0716-1554-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2021
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:19:48 | 只看該作者
Methods in Molecular Biologyhttp://image.papertrans.cn/e/image/313090.jpg
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發(fā)表于 2025-3-22 02:44:20 | 只看該作者
https://doi.org/10.1007/978-1-0716-1554-6Kinetic models; Drug-drug interactions; Drug metabolizing enzymes; Regulatory guidelines; Drug transport
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Africa-EU Partnership on Energy major cause of clinically significant drug–drug interactions. This chapter defines the four reversible mechanisms of inhibition exhibited by drugs: competitive, noncompetitive, uncompetitive, and mixed competitive/noncompetitive. An in vitro procedure to determine the potential of a drug to be a re
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發(fā)表于 2025-3-22 16:36:35 | 只看該作者
A. M. Vasiliev,D. A. Degterev,T. M. Shawt a million compared to the rate of the same reaction in the absence of the enzyme. In contrast to traditional catalytic enzymes, the family of cytochrome P450 (CYPs) enzymes are catalytically promiscuous and thus they possess remarkable versatility in substrates. The great diversity of reactions ca
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發(fā)表于 2025-3-22 19:58:06 | 只看該作者
Célestine L. D. Mangue,Jean Gonondoe. In all but the very simplest in vitro system, these drug concentrations can be influenced by a variety of nonspecific binding reservoirs that can reduce the available concentration to the enzyme system(s) under investigation. As a consequence, the apparent kinetic parameters, such as . or ., that
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Imperialism and U.S.-Africa Relationsf their crystallographic protein structures. Fortunately, despite low sequence similarity between different families of drug-metabolizing CYPs, there exists a high degree of structural homology within the superfamily. This similarity in the protein fold allows for a direct comparison of the structur
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發(fā)表于 2025-3-23 08:32:34 | 只看該作者
https://doi.org/10.1007/978-1-349-06218-8hey translocate drugs, as well as endogenous molecules and toxins, across membranes using ATP hydrolysis, or ion/concentration gradients. In general, drug transporters are expressed ubiquitously, but they function in drug disposition by being concentrated in tissues such as the intestine, the kidney
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