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	<title>Translations:Discovery and development of angiotensin receptor blockers/43/en - Revision history</title>
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	<updated>2026-08-15T02:54:43Z</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;==ARBs under development==&lt;br /&gt;
[[File:Pratosartan.svg|right|thumb|[[Pratosartan]] structure.]]&lt;br /&gt;
Several new nonpeptide ARBs are undergoing [[clinical trials]] or are at pre-clinical stages of development. Among these are [[embusartan]] (BAY 10-6734 or BAY 10-6734), KRH-594, [[fonsartan]] (HR 720) and [[pratosartan]] (KT3-671). Pratosartan, for example, has a novel structure: a seven-membered ring that bears an [[Ketone|oxo]] moiety (C=O) fused to the imidazole ring (figure 4), and its affinity for the AT&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; receptor is about 7 times higher than  losartan&amp;#039;s. The purpose of the [[Ketone|oxo]] group is similar to that of the carboxylic acid groups on other ARBs.&amp;lt;br /&amp;gt;&lt;br /&gt;
Other attributes of ARBs are also under investigation, such as the positive effects of telmisartan on [[lipid metabolism|lipid]] and [[glucose metabolism]] and losartan&amp;#039;s effects of lowering [[uric acid]] levels. Such effects might lead to new indications for these drugs but further research is needed.&lt;/div&gt;</summary>
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