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	<title>Translations:Discovery and development of angiotensin receptor blockers/25/en - Revision history</title>
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	<updated>2026-07-13T11:38:12Z</updated>
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		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2024-03-28T01:25:31Z</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;Replacing the 2-carboxy-benzamido-group with a 2-carboxy-[[phenyl]]-group created the [[lipophilic]] [[biphenyl]]-containing EXP-7711, which exhibited good oral activity but slightly less affinity for the AT&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; receptor. &amp;lt;br /&amp;gt;&lt;br /&gt;
 &lt;br /&gt;
Then the [[chemical polarity|polar]] carboxyl group was replaced with a more lipophilic [[tetrazole]] group in order to increase oral bioavailability and duration of action further and the compound thus formed was named [[losartan]]. This development took place in 1986 and losartan became the first successful [[angiotensin II receptor antagonist|Ang II antagonist]] drug, approved as such in the United States in 1995 and was marketed by [[Merck &amp;amp; Co.|Merck]].&lt;/div&gt;</summary>
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