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	<title>Translations:7-Dehydrocholesterol/1/ja - Revision history</title>
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	<updated>2026-05-12T13:46:18Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>Fire: Created page with &quot;{{chembox | Verifiedfields = changed | verifiedrevid = 477226494 | ImageFile = 7-Dehydrocholesterol.svg | ImageSize = 220 | ImageFile1 = 7-Dehydrocholesterol molecule ball.png | ImageSize1 = 250 | ImageAlt1 = 7-デヒドロコレステロールのボール＆スティックモデル | IUPACName = Cholesta-5,7-dien-3β-ol | SystematicName = (1&#039;&#039;R&#039;&#039;,3a&#039;&#039;R&#039;&#039;,7&#039;&#039;S&#039;&#039;,9a&#039;&#039;R&#039;&#039;,9b&#039;&#039;S&#039;&#039;,11a&#039;&#039;R&#039;&#039;)-9a,11a-Dimethyl-1-[(2&#039;&#039;R&#039;&#039;)-6-methylheptan-2-yl]-2,3,3a,6,7,8,9,9a,9b,10,11,11a-dode...&quot;</title>
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		<updated>2024-04-11T10:08:42Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;{{chembox | Verifiedfields = changed | verifiedrevid = 477226494 | ImageFile = 7-Dehydrocholesterol.svg | ImageSize = 220 | ImageFile1 = 7-Dehydrocholesterol molecule ball.png | ImageSize1 = 250 | ImageAlt1 = 7-デヒドロコレステロールのボール＆スティックモデル | IUPACName = Cholesta-5,7-dien-3β-ol | SystematicName = (1&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,3a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,7&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,9a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,9b&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,11a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-9a,11a-Dimethyl-1-[(2&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-6-methylheptan-2-yl]-2,3,3a,6,7,8,9,9a,9b,10,11,11a-dode...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{chembox&lt;br /&gt;
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| ImageFile1 = 7-Dehydrocholesterol molecule ball.png&lt;br /&gt;
| ImageSize1 = 250&lt;br /&gt;
| ImageAlt1 = 7-デヒドロコレステロールのボール＆スティックモデル&lt;br /&gt;
| IUPACName = Cholesta-5,7-dien-3β-ol&lt;br /&gt;
| SystematicName = (1&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,3a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,7&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,9a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,9b&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,11a&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-9a,11a-Dimethyl-1-[(2&amp;#039;&amp;#039;R&amp;#039;&amp;#039;)-6-methylheptan-2-yl]-2,3,3a,6,7,8,9,9a,9b,10,11,11a-dodecahydro-1&amp;#039;&amp;#039;H&amp;#039;&amp;#039;-cyclopenta[&amp;#039;&amp;#039;a&amp;#039;&amp;#039;]phenanthren-7-ol&lt;br /&gt;
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}&lt;br /&gt;
| ChemSpiderID = 388534&lt;br /&gt;
| InChI = 1/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3/t19-,21+,23-,24+,25+,26+,27-/m1/s1&lt;br /&gt;
| InChIKey = UCTLRSWJYQTBFZ-DDPQNLDTBZ&lt;br /&gt;
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}&lt;br /&gt;
| StdInChI = 1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3/t19-,21+,23-,24+,25+,26+,27-/m1/s1-dehydrocholesterol &lt;br /&gt;
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}&lt;br /&gt;
| StdInChIKey = UCTLRSWJYQTBFZ-DDPQNLDTSA-N&lt;br /&gt;
| CASNo_Ref = {{cascite|correct|CAS}}&lt;br /&gt;
| CASNo = 434-16-2&lt;br /&gt;
| PubChem = 172&lt;br /&gt;
| UNII_Ref = {{fdacite|correct|FDA}}&lt;br /&gt;
| UNII = BK1IU07GKF&lt;br /&gt;
| ChEBI_Ref = {{ebicite|correct|EBI}}&lt;br /&gt;
| ChEBI = 17759&lt;br /&gt;
| SMILES = O[C@@H]4C/C3=C/C=C1\[C@H](CC[C@]2([C@H]1CC[C@@H]2[C@H](C)CCCC(C)C)C)[C@@]3(C)CC4&lt;br /&gt;
| MeSHName = 7-dehydrocholesterol&lt;br /&gt;
  }}&lt;br /&gt;
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[[Image:Skinlayers.png|thumb|250px|right|皮膚の表皮層]] &lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;7-デヒドロコレステロール&amp;#039;&amp;#039;&amp;#039;（&amp;#039;&amp;#039;&amp;#039;7-DHC&amp;#039;&amp;#039;&amp;#039;）は[[zoosterol/ja|動物ステロール]]の一種で、[[blood plasma/ja|血清]]では[[cholesterol/ja|コレステロール]]前駆体として機能し、[[skin/ja|皮膚]]では[[photochemically/ja|光化学的]]に[[Cholecalciferol/ja||ビタミンD&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;]]に変換されるため、[[provitamin/ja|プロビタミン]]-D&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;として機能する。ヒトの皮膚にこの化合物が存在することで、ヒトはビタミンD&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;（[[cholecalciferol/ja|コレカルシフェロール]]）を製造することができる。 [[ultraviolet/ja|紫外線]]を浴びると、ビタミンDは生成される。太陽光に含まれる[[UV-B]]を浴びると、7-DHCは中間[[異性体]]として[[Previtamin D3/ja|プレビタミンD&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;]]を経由してビタミンD&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;に変換される。また、いくつかの哺乳類の[[milk/ja|乳]]にも含まれている。羊毛を持つ哺乳類が自然に分泌する[[lanolin/ja|ラノリン]]という蝋状の物質には7-DHCが含まれており、日光によってビタミンDに変換され、毛づくろいの際に栄養素として摂取される。昆虫では、7-デヒドロコレステロールは成虫になるために必要なホルモン[[ecdysone/ja|エクダイソン]]の前駆体である。ノーベル賞受賞の有機化学者[[:en:Adolf Windaus|アドルフ・ウィンダウス]]によって発見された。&lt;/div&gt;</summary>
		<author><name>Fire</name></author>
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