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	<title>Translations:Discovery and development of angiotensin receptor blockers/23/en - Revision history</title>
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	<updated>2026-11-10T06:19:52Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wiki.tiffa.net/w/index.php?title=Translations:Discovery_and_development_of_angiotensin_receptor_blockers/23/en&amp;diff=131480&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;Using [[nuclear magnetic resonance]] studies on the spatial structure of Ang II, scientists at DuPont discovered that the Takeda structures had to be enlarged at a particular position to resemble more closely the much larger peptide Ang II.&lt;br /&gt;
Computer modeling was used to compare S-8308 and S-8307 with Ang II and it was seen that Ang II contains two [[acidic]] residues near the NH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; terminus. These groups were not mimicked by the Takeda leads and therefore it was hypothesized that acidic [[functional groups]] would have to be added to the compounds.&amp;lt;br /&amp;gt;&lt;br /&gt;
The 4-carboxy-derivative EXP-6155 had a binding activity which was ten-fold greater than that of S-8308 which further strengthened this [[hypothesis]].&lt;/div&gt;</summary>
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