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Titlebook: Drug Discovery and Development; Michael Williams,Jeffrey B. Malick Book 1987 The Humana Press Inc. 1987 autoimmune disease.cannabinoid.dev

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發(fā)表于 2025-3-21 16:21:58 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Drug Discovery and Development
編輯Michael Williams,Jeffrey B. Malick
視頻videohttp://file.papertrans.cn/284/283067/283067.mp4
圖書封面Titlebook: Drug Discovery and Development;  Michael Williams,Jeffrey B. Malick Book 1987 The Humana Press Inc. 1987 autoimmune disease.cannabinoid.dev
出版日期Book 1987
關(guān)鍵詞autoimmune disease; cannabinoid; development; drug; drug discovery; drugs; dynamics; ethanol; methodology; ne
版次1
doihttps://doi.org/10.1007/978-1-4612-4828-6
isbn_softcover978-1-4612-9180-0
isbn_ebook978-1-4612-4828-6
copyrightThe Humana Press Inc. 1987
The information of publication is updating

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發(fā)表于 2025-3-21 22:00:42 | 只看該作者
Aufgaben und Werkzeuge der Verdauungwide use and acceptance. The science surrounding these dosage forms has progressed significantly in terms of the knowledge required to make better tablets, to understand the role of disintegrants, and to optimize inert ingredient ratios through sophisticated formulation design (Lachman et al., 1976; Lieberman and Lachman, 1980).
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發(fā)表于 2025-3-22 01:32:26 | 只看該作者
Biochemical Approaches for Evaluating Drug—Receptor Interactionsn be used for analyzing dozens of compounds in a matter of hours. By providing the pharmacologist and chemist with information about potency, efficacy, and structure-activity characteristics, this methodology enables them to select a few lead agents that can then be subjected to more detailed examination in secondary and tertiary screens.
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Drug Discovery at the Enzyme Levelir efficacy. We will consider how enzyme activity is assayed, how inhibitors are found (or made) and characterized, how enzyme inhibition is demonstrated in vivo, and some specific examples of enzyme inhibitors that are used as drugs.
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發(fā)表于 2025-3-22 23:17:01 | 只看該作者
Immunopharmacological Approaches to Drug Developmente biological and biochemical effects of synthetic and natural products on immune responsiveness, elucidate the mechanism(s) through which such effects are mediated, and evaluate the clinical potential of such agents.
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Drug Designhis strategy and dictate the type of approach; that is, either a rational or an empirical one. Depending on this selection, the synthetic targets then will either be derived from drug design concepts for the former or developed around systematic variation of a lead compound for the latter.
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