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	<title>Translations:Vitamin D5/1/en - Revision history</title>
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	<updated>2026-05-12T10:09:21Z</updated>
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		<id>https://wiki.tiffa.net/w/index.php?title=Translations:Vitamin_D5/1/en&amp;diff=136987&amp;oldid=prev</id>
		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2024-04-10T12:36:42Z</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;{{short description|Fat soluble vitamin}}{{DISPLAYTITLE:Vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;}}&lt;br /&gt;
{{chembox&lt;br /&gt;
| Verifiedfields = changed&lt;br /&gt;
| verifiedrevid = 470631138&lt;br /&gt;
| Name=Vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;&lt;br /&gt;
| ImageFile=Vitamin D5 structure.svg&lt;br /&gt;
| ImageSize=&lt;br /&gt;
| IUPACName=(1&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,3&amp;#039;&amp;#039;Z&amp;#039;&amp;#039;)-3-[(2&amp;#039;&amp;#039;E&amp;#039;&amp;#039;)-2-[(1&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,3a&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,7a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-1-[(1&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,4&amp;#039;&amp;#039;S&amp;#039;&amp;#039;)-4-ethyl-1,5-dimethylhexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1&amp;#039;&amp;#039;H&amp;#039;&amp;#039;-inden-4-ylidene]ethylidene]-4-methylene-1-cyclohexanol&lt;br /&gt;
| OtherNames= Sitocalciferol &amp;lt;br&amp;gt; (5&amp;#039;&amp;#039;Z&amp;#039;&amp;#039;,7&amp;#039;&amp;#039;E&amp;#039;&amp;#039;)-(3&amp;#039;&amp;#039;S&amp;#039;&amp;#039;)-9,10-secoporiferasta-5,7,10(19)-trien-3-ol&lt;br /&gt;
|Section1={{Chembox Identifiers&lt;br /&gt;
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}&lt;br /&gt;
| ChemSpiderID = 7826639&lt;br /&gt;
| ChEBI = 33279&lt;br /&gt;
| InChI = 1/C29H48O/c1-7-23(20(2)3)12-10-22(5)27-16-17-28-24(9-8-18-29(27,28)6)13-14-25-19-26(30)15-11-21(25)4/h13-14,20,22-23,26-28,30H,4,7-12,15-19H2,1-3,5-6H3/b24-13+,25-14-/t22-,23+,26+,27-,28+,29-/m1/s1&lt;br /&gt;
| InChIKey = RMDJVOZETBHEAR-GHTRHTQZBN&lt;br /&gt;
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}&lt;br /&gt;
| StdInChI = 1S/C29H48O/c1-7-23(20(2)3)12-10-22(5)27-16-17-28-24(9-8-18-29(27,28)6)13-14-25-19-26(30)15-11-21(25)4/h13-14,20,22-23,26-28,30H,4,7-12,15-19H2,1-3,5-6H3/b24-13+,25-14-/t22-,23+,26+,27-,28+,29-/m1/s1&lt;br /&gt;
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}&lt;br /&gt;
| StdInChIKey = RMDJVOZETBHEAR-GHTRHTQZSA-N&lt;br /&gt;
| CASNo_Ref = {{cascite|correct|CAS}}&lt;br /&gt;
| CASNo=71761-06-3&lt;br /&gt;
| UNII_Ref = {{fdacite|correct|FDA}}&lt;br /&gt;
| UNII = 0W2I161LCL&lt;br /&gt;
| PubChem=9547700&lt;br /&gt;
| SMILES = O[C@@H]1CC(\C(=C)CC1)=C\C=C2/CCC[C@]3([C@H]2CC[C@@H]3[C@H](C)CC[C@H](CC)C(C)C)C&lt;br /&gt;
}}&lt;br /&gt;
|Section2={{Chembox Properties&lt;br /&gt;
| C=29 | H=48 | O=1&lt;br /&gt;
| Appearance=&lt;br /&gt;
| Density=&lt;br /&gt;
| MeltingPt=&lt;br /&gt;
| BoilingPt=&lt;br /&gt;
| Solubility=&lt;br /&gt;
  }}&lt;br /&gt;
|Section3={{Chembox Hazards&lt;br /&gt;
| MainHazards=&lt;br /&gt;
| FlashPt=&lt;br /&gt;
| AutoignitionPt =&lt;br /&gt;
  }}&lt;br /&gt;
}}&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;sitocalciferol&amp;#039;&amp;#039;&amp;#039;) is a form of [[vitamin D]].&lt;br /&gt;
== Research ==&lt;br /&gt;
[[structural analog|Analogs]] of [[calcitriol]], a form of vitamin D&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, have been proposed for use as antitumor agents. Studies on vitamin D&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; have shown inhibition of cell proliferation in [[prostate cancer]], but high doses of vitamin D&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt; result in [[Hypercalcaemia|hypercalcemia]]. The effects of vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt; on prostate cancer have also been studied, and unlike vitamin D&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;, vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt; does not cause [[Hypercalcaemia|hypercalcemia]] while inhibiting tumor cell proliferation. The most researched analogue of vitamin D&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt; as an antitumor agent is 1α-hydroxyvitamin D&amp;lt;sub&amp;gt;5.&amp;lt;/sub&amp;gt;&lt;/div&gt;</summary>
		<author><name>FuzzyBot</name></author>
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