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Titlebook: Discovery DMPK Quick Guide; Guide to Data Interp S. Cyrus Khojasteh,Harvey Wong,Cornelis E.C.A. Hop Book 2022 Springer Nature Switzerland A

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21#
發(fā)表于 2025-3-25 04:15:00 | 只看該作者
22#
發(fā)表于 2025-3-25 08:46:17 | 只看該作者
l for day-to-day interpretation of ADME studies.Multi discip.This book is intended for a broad readership,?in particular,?those working or interested in drug discovery coming from various disciplines such as medicinal chemistry, pharmacology, drug metabolism and pharmacokinetics, bioanalysis, clinic
23#
發(fā)表于 2025-3-25 13:48:36 | 只看該作者
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發(fā)表于 2025-3-25 18:57:05 | 只看該作者
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發(fā)表于 2025-3-25 23:19:12 | 只看該作者
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發(fā)表于 2025-3-26 01:47:04 | 只看該作者
27#
發(fā)表于 2025-3-26 05:36:03 | 只看該作者
28#
發(fā)表于 2025-3-26 11:43:00 | 只看該作者
Goals for DMPK During Drug Optimizations,f a molecule’s interaction/modulation of a therapeutic target. What allows conversion of a potent chemical starting point to a final drug/drug candidate during the optimization process is the incorporation of appropriate ADME properties that balance efficacy and toxicity. Here we capture the high-le
29#
發(fā)表于 2025-3-26 14:29:56 | 只看該作者
Drug Properties, (1) an inability to demonstrate that the target can modulate the disease in a preclinical model, (2) the lack of a therapeutic index to modulate the target safely or (3) the inability to find molecules with the right balance of properties such as potency, selectivity, ADME properties, safety endpoi
30#
發(fā)表于 2025-3-26 17:42:35 | 只看該作者
DMPK Lead Optimization, optimization of molecules based on key ADME attributes. This has had a huge impact on the molecular design cycles: design, synthesis, assessment and re-design..In this chapter, we discuss the strategies for optimization of small molecules during drug discovery and address various ADME liabilities t
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