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	<title>Translations:Discovery and development of angiotensin receptor blockers/36/en - Revision history</title>
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	<updated>2026-11-10T06:19:51Z</updated>
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		<id>https://wiki.tiffa.net/w/index.php?title=Translations:Discovery_and_development_of_angiotensin_receptor_blockers/36/en&amp;diff=131493&amp;oldid=prev</id>
		<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;===Pharmacophore and structure-activity relationship===&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Pharmacophore&amp;#039;&amp;#039;&amp;#039;&amp;lt;br /&amp;gt;&lt;br /&gt;
There are three functional groups that are the most important parts for the [[bioactivity]] of ARBs, see figure 1 for details.&amp;lt;br /&amp;gt;&lt;br /&gt;
The first one is the imidazole ring that binds to amino acids in helix 7 ([[Asparagine|Asn]]&amp;lt;sup&amp;gt;295&amp;lt;/sup&amp;gt;). The second group is the biphenyl-methyl group that binds to amino acids in both helices 6 and 7 ([[Phenylalanine|Phe]]&amp;lt;sup&amp;gt;301&amp;lt;/sup&amp;gt;, [[Phenylalanine|Phe]]&amp;lt;sup&amp;gt;300&amp;lt;/sup&amp;gt;, [[Tryptophan|Trp]]&amp;lt;sup&amp;gt;253&amp;lt;/sup&amp;gt; and [[Histidine|His]]&amp;lt;sup&amp;gt;256&amp;lt;/sup&amp;gt;). The third one is the [[tetrazole]] group that interacts with amino acids in helices 4 and 5 ([[Arginine|Arg]]&amp;lt;sup&amp;gt;167&amp;lt;/sup&amp;gt; and [[Lysine|Lys]]&amp;lt;sup&amp;gt;199&amp;lt;/sup&amp;gt;). &amp;lt;br /&amp;gt;&lt;br /&gt;
The tetrazole group has been successfully replaced by a carboxylic acid group as is the case with telmisartan.&lt;/div&gt;</summary>
		<author><name>FuzzyBot</name></author>
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