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	<title>8β-VE2 - Revision history</title>
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		<updated>2024-05-22T16:31:03Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:8-vinylestradiol_structure.png|thumb|8-vinylestradiol_structure.png]] {{Short description|Synthetic estrogen}}&lt;br /&gt;
{{Infobox drug&lt;br /&gt;
| IUPAC_name = (8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol&lt;br /&gt;
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| synonyms = 8β-Vinylestradiol&lt;br /&gt;
| CAS_number = 123456-78-9&lt;br /&gt;
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| chemical_formula = C_18H_24O_2&lt;br /&gt;
| molecular_weight = 272.38&lt;br /&gt;
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}}&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;8β-VE2&amp;#039;&amp;#039;&amp;#039; (8β-Vinylestradiol) is a synthetic [[estrogen]] and a derivative of [[estradiol]]. It is characterized by the presence of a vinyl group at the 8β position of the [[estradiol]] molecule. This modification alters its [[pharmacokinetics]] and [[pharmacodynamics]] compared to natural [[estradiol]].&lt;br /&gt;
&lt;br /&gt;
==Chemical Structure==&lt;br /&gt;
8β-VE2 has the chemical formula C_18H_24O_2 and a molecular weight of 272.38 g/mol. The IUPAC name for 8β-VE2 is (8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol.&lt;br /&gt;
&lt;br /&gt;
==Pharmacology==&lt;br /&gt;
8β-VE2 acts as an [[agonist]] of the [[estrogen receptor]]s, similar to [[estradiol]]. However, the presence of the vinyl group at the 8β position may influence its binding affinity and activity at the receptor level. This can result in different [[pharmacokinetic]] and [[pharmacodynamic]] properties compared to natural [[estradiol]].&lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
8β-VE2 is primarily used in [[research]] settings to study the effects of modified estrogens on various biological systems. It is not commonly used in clinical practice.&lt;br /&gt;
&lt;br /&gt;
==Synthesis==&lt;br /&gt;
The synthesis of 8β-VE2 involves the chemical modification of [[estradiol]] to introduce a vinyl group at the 8β position. This process typically requires several steps, including protection and deprotection of functional groups, as well as selective reactions to achieve the desired modification.&lt;br /&gt;
&lt;br /&gt;
==Related Compounds==&lt;br /&gt;
* [[Estradiol]]&lt;br /&gt;
* [[Ethinylestradiol]]&lt;br /&gt;
* [[Mestranol]]&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
* [[Estrogen]]&lt;br /&gt;
* [[Estrogen receptor]]&lt;br /&gt;
* [[Hormone replacement therapy]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Estrogens]]&lt;br /&gt;
[[Category:Synthetic hormones]]&lt;br /&gt;
[[Category:Research chemicals]]&lt;br /&gt;
[[Category:Steroids]]&lt;br /&gt;
&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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