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	<title>Doc:9,11,13-Octadecatrienoic acid - Revision history</title>
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	<updated>2026-04-29T14:49:54Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21229&amp;oldid=prev</id>
		<title>Editor at 08:52, 29 September 2010</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21229&amp;oldid=prev"/>
		<updated>2010-09-29T08:52:28Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
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				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 17:52, 29 September 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l4&quot;&gt;Line 4:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 4:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;３つある二重結合の構造異性体は８種類考えられるが、４種が天然に見つかっている。&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;３つある二重結合の構造異性体は８種類考えられるが、４種が天然に見つかっている。&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;;&amp;amp;alpha;-eleostearic acid (cis, trans, trans) m.p. 48 °C&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;;&amp;amp;alpha;-eleostearic acid (cis, trans, trans) &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[LBF18305SC02]] &lt;/ins&gt;m.p. 48 °C&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;The most common acid of this group. Principal acid of tung oil or China Wood oil, and the seed oil of [http://metabolomics.jp/wiki/Species:Momordica &amp;#039;&amp;#039;Momordica charantia&amp;#039;&amp;#039;] and [http://metabolomics.jp/wiki/Species:Centranthus &amp;#039;&amp;#039;Centranthus macrosiphon&amp;#039;&amp;#039;]. It is easily converted to &amp;amp;beta;-eleostearic acid by light, heat, sulfur, acid, or iodine.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;The most common acid of this group. Principal acid of tung oil or China Wood oil, and the seed oil of [http://metabolomics.jp/wiki/Species:Momordica &amp;#039;&amp;#039;Momordica charantia&amp;#039;&amp;#039;] and [http://metabolomics.jp/wiki/Species:Centranthus &amp;#039;&amp;#039;Centranthus macrosiphon&amp;#039;&amp;#039;]. It is easily converted to &amp;amp;beta;-eleostearic acid by light, heat, sulfur, acid, or iodine.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l12&quot;&gt;Line 12:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 12:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; Punicic acid (cis, trans, cis) m.p. 41 °C&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; Punicic acid (cis, trans, cis) &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[LBF18305SC01]]  &lt;/ins&gt;m.p. 41 °C&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Principal acid of [http://metabolomics.jp/wiki/Species:Punica pomegranate] seed oil. Yellow. It is easily coverted to &amp;amp;beta;-eleostearic acid by the same catalysts. Its alternative name is Trichosanic acid, a major component of [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] seed oil. It shows platelet aggregation &amp;lt;ref&amp;gt;Takenaga M, Hirai A, Terano T, Tamura Y, Kitagawa H, Yoshida S (1988) &amp;quot;In vitro effect of trichosanic acid, a major component of Trichosanthes japonica on platelet aggregation and arachidonic acid metabolism in human platelets&amp;quot; &amp;#039;&amp;#039;Prostaglandins Leukot Essent Fatty Acids&amp;#039;&amp;#039; 31(2):65-72&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Principal acid of [http://metabolomics.jp/wiki/Species:Punica pomegranate] seed oil. Yellow. It is easily coverted to &amp;amp;beta;-eleostearic acid by the same catalysts. Its alternative name is Trichosanic acid, a major component of [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] seed oil. It shows platelet aggregation &amp;lt;ref&amp;gt;Takenaga M, Hirai A, Terano T, Tamura Y, Kitagawa H, Yoshida S (1988) &amp;quot;In vitro effect of trichosanic acid, a major component of Trichosanthes japonica on platelet aggregation and arachidonic acid metabolism in human platelets&amp;quot; &amp;#039;&amp;#039;Prostaglandins Leukot Essent Fatty Acids&amp;#039;&amp;#039; 31(2):65-72&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l24&quot;&gt;Line 24:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 24:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; &amp;amp;beta;-eleostearic acid (trans, trans, trans) m.p. 72 °C&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; &amp;amp;beta;-eleostearic acid (trans, trans, trans) &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[LBF18305SC03]] &lt;/ins&gt;m.p. 72 °C&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{Twocolumn|&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Transformed form of &amp;amp;alpha;-eleostearic acid or punicic acid.&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Transformed form of &amp;amp;alpha;-eleostearic acid or punicic acid.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;

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		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21228&amp;oldid=prev</id>
		<title>Editor at 08:51, 29 September 2010</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21228&amp;oldid=prev"/>
		<updated>2010-09-29T08:51:12Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 17:51, 29 September 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l25&quot;&gt;Line 25:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 25:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; &amp;amp;beta;-eleostearic acid (trans, trans, trans) m.p. 72 °C&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; &amp;amp;beta;-eleostearic acid (trans, trans, trans) m.p. 72 °C&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;{{Twocolumn|&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Transformed form of &amp;amp;alpha;-eleostearic acid or punicic acid.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;|&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;amp;alpha;-eleostearic acid や punicic acid が変化したもの。&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;}}&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; Catalpic acid (trans, trans, cis) m.p. 32 °C&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;; Catalpic acid (trans, trans, cis) m.p. 32 °C&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;

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&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21227&amp;oldid=prev</id>
		<title>Editor at 08:48, 29 September 2010</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21227&amp;oldid=prev"/>
		<updated>2010-09-29T08:48:36Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 17:48, 29 September 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l21&quot;&gt;Line 21:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 21:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[http://metabolomics.jp/wiki/Species:Punica ザクロ] の種から取れる黄色い油の主成分。ザクロの属名 Punica より名がついている。 &amp;amp;alpha;-eleostearic acidと同様に、同じ触媒によって簡単に &amp;amp;beta;-eleostearic acid に変化する。別名は  Trichosanic acid で、日本のでヘビウリと呼ばれる [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] 種子の主成分。血小板の凝固作用がある。&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[http://metabolomics.jp/wiki/Species:Punica ザクロ] の種から取れる黄色い油の主成分。ザクロの属名 Punica より名がついている。 &amp;amp;alpha;-eleostearic acidと同様に、同じ触媒によって簡単に &amp;amp;beta;-eleostearic acid に変化する。別名は  Trichosanic acid で、日本のでヘビウリと呼ばれる [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] 種子の主成分。血小板の凝固作用がある。&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;:最近の文献では (trans, cis, trans)-型がザクロ[http://metabolomics.jp/wiki/Species:Punica &#039;&#039;Punica granatum&#039;&#039;])種子油の主成分で88%を占めると報告されている。この結果はこれまでの研究(Punicic acid が主成分と異なるため、間違いではないかと思われる。 {{WrittenBy|&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Masanori Arita&lt;/del&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;:最近の文献では (trans, cis, trans)-型がザクロ[http://metabolomics.jp/wiki/Species:Punica &#039;&#039;Punica granatum&#039;&#039;])種子油の主成分で88%を占めると報告されている。この結果はこれまでの研究(Punicic acid が主成分と異なるため、間違いではないかと思われる。 {{WrittenBy|&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;有田正規&lt;/ins&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;

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&lt;/table&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21226&amp;oldid=prev</id>
		<title>Editor: New page: {{Twocolumn| There are 8 possible isomers, and 4 are naturally identified. | ３つある二重結合の構造異性体は８種類考えられるが、４種が天然に見つかってい...</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=Doc:9,11,13-Octadecatrienoic_acid&amp;diff=21226&amp;oldid=prev"/>
		<updated>2010-09-29T08:47:13Z</updated>

		<summary type="html">&lt;p&gt;New page: {{Twocolumn| There are 8 possible isomers, and 4 are naturally identified. | ３つある二重結合の構造異性体は８種類考えられるが、４種が天然に見つかってい...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Twocolumn|&lt;br /&gt;
There are 8 possible isomers, and 4 are naturally identified.&lt;br /&gt;
|&lt;br /&gt;
３つある二重結合の構造異性体は８種類考えられるが、４種が天然に見つかっている。&lt;br /&gt;
}}&lt;br /&gt;
;&amp;amp;alpha;-eleostearic acid (cis, trans, trans) m.p. 48 °C&lt;br /&gt;
{{Twocolumn|&lt;br /&gt;
The most common acid of this group. Principal acid of tung oil or China Wood oil, and the seed oil of [http://metabolomics.jp/wiki/Species:Momordica &amp;#039;&amp;#039;Momordica charantia&amp;#039;&amp;#039;] and [http://metabolomics.jp/wiki/Species:Centranthus &amp;#039;&amp;#039;Centranthus macrosiphon&amp;#039;&amp;#039;]. It is easily converted to &amp;amp;beta;-eleostearic acid by light, heat, sulfur, acid, or iodine.&lt;br /&gt;
|&lt;br /&gt;
もっとも一般的で、ツング（中国では四川省に生える油桐）油、&lt;br /&gt;
[http://metabolomics.jp/wiki/Species:Momordica &amp;#039;&amp;#039;Momordica charantia&amp;#039;&amp;#039;] や [http://metabolomics.jp/wiki/Species:Centranthus &amp;#039;&amp;#039;Centranthus macrosiphon&amp;#039;&amp;#039;] の種から取れる油の主成分。光や熱、硫黄、酸、ヨウ素などによって容易に &amp;amp;beta;-eleostearic acid に変化する。 &lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
; Punicic acid (cis, trans, cis) m.p. 41 °C&lt;br /&gt;
{{Twocolumn|&lt;br /&gt;
Principal acid of [http://metabolomics.jp/wiki/Species:Punica pomegranate] seed oil. Yellow. It is easily coverted to &amp;amp;beta;-eleostearic acid by the same catalysts. Its alternative name is Trichosanic acid, a major component of [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] seed oil. It shows platelet aggregation &amp;lt;ref&amp;gt;Takenaga M, Hirai A, Terano T, Tamura Y, Kitagawa H, Yoshida S (1988) &amp;quot;In vitro effect of trichosanic acid, a major component of Trichosanthes japonica on platelet aggregation and arachidonic acid metabolism in human platelets&amp;quot; &amp;#039;&amp;#039;Prostaglandins Leukot Essent Fatty Acids&amp;#039;&amp;#039; 31(2):65-72&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
:In a recent article&amp;lt;ref&amp;gt;Fatope MO, Al Burtomani SK, Takeda Y (2002) &amp;quot;Monoacylglycerol from Punica granatum Seed Oil&amp;quot; &amp;#039;&amp;#039;J Agric Food Chem&amp;#039;&amp;#039; 50:357-360&amp;lt;/ref&amp;gt;, (trans, cis, trans)-form was isolated from pomegranate ([http://metabolomics.jp/wiki/Species:Punica &amp;#039;&amp;#039;Punica granatum&amp;#039;&amp;#039;] seed and it constituted about 88% of the seed oil.&lt;br /&gt;
The result contradicts other results (Punicic acid is major, e.g. &amp;lt;ref&amp;gt;Kyralan M, Golukcu M, Tokgoz H (2009) &amp;quot;Oil and Conjugated Linolenic Acid Contents of Seeds from Important Pomegranate Cultivars (Punica granatum L.) Grown in Turkey&amp;quot; &amp;#039;&amp;#039;J Am Oil Chem Soc&amp;#039;&amp;#039; 86:985–990&amp;lt;/ref&amp;gt;), and is considered an error. {{WrittenBy|Masanori Arita}}&lt;br /&gt;
|&lt;br /&gt;
[http://metabolomics.jp/wiki/Species:Punica ザクロ] の種から取れる黄色い油の主成分。ザクロの属名 Punica より名がついている。 &amp;amp;alpha;-eleostearic acidと同様に、同じ触媒によって簡単に &amp;amp;beta;-eleostearic acid に変化する。別名は  Trichosanic acid で、日本のでヘビウリと呼ばれる [http://metabolomics.jp/wiki/Species:Trichosanthes &amp;#039;&amp;#039;Trichosanthes kirilowii japonica&amp;#039;&amp;#039;] 種子の主成分。血小板の凝固作用がある。&lt;br /&gt;
&lt;br /&gt;
:最近の文献では (trans, cis, trans)-型がザクロ[http://metabolomics.jp/wiki/Species:Punica &amp;#039;&amp;#039;Punica granatum&amp;#039;&amp;#039;])種子油の主成分で88%を占めると報告されている。この結果はこれまでの研究(Punicic acid が主成分と異なるため、間違いではないかと思われる。 {{WrittenBy|Masanori Arita}}&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
; &amp;amp;beta;-eleostearic acid (trans, trans, trans) m.p. 72 °C&lt;br /&gt;
&lt;br /&gt;
; Catalpic acid (trans, trans, cis) m.p. 32 °C&lt;br /&gt;
{{Twocolumn|&lt;br /&gt;
Principal acid of [http://metabolomics.jp/wiki/Species:Catalpa &amp;#039;&amp;#039;Catalpa ovata, Catalpa speciosa&amp;#039;&amp;#039; and &amp;#039;&amp;#039;Catalpa bignonioides&amp;#039;&amp;#039;] seed oil.&lt;br /&gt;
|&lt;br /&gt;
[http://metabolomics.jp/wiki/Species:Catalpa &amp;#039;&amp;#039;Catalpa ovata, Catalpa speciosa&amp;#039;&amp;#039; や &amp;#039;&amp;#039;Catalpa bignonioides&amp;#039;&amp;#039;] 種子油の主成分。&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
;References&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
</feed>