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	<title>Translations:Medication/73/en - Revision history</title>
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	<updated>2026-04-19T05:56:58Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2023-01-22T00:47:52Z</updated>

		<summary type="html">&lt;p&gt;Importing a new version from external source&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Modern drug discovery involves the identification of screening hits, [[medicinal chemistry|medicinal chemistry]] and optimization of those hits to increase the [[Affinity (pharmacology)#Protein-ligand binding|affinity]], [[binding selectivity|selectivity]] (to reduce the potential of side effects), efficacy/[[potency (pharmacology)|potency]], [[Metabolism|metabolic]] stability (to increase the [[Biological half-life|half-life]]), and oral [[bioavailability|bioavailability]]. Once a compound that fulfills all of these requirements has been identified, it will begin the process of [[drug development|drug development]] prior to [[clinical trial|clinical trial]]s. One or more of these steps may, but not necessarily, involve [[computer-aided drug design|computer-aided drug design]].&lt;/div&gt;</summary>
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