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	<title>LBF20406HP08 - Revision history</title>
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	<updated>2026-05-30T17:44:05Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBF20406HP08&amp;diff=55645&amp;oldid=prev</id>
		<title>Editor: New page: {{Lipid/Header}}  {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |LipidBank=DFA8087 |LipidMaps=LMFA03060046 |SysName=5,12-Dihydroperoxy-6,8,10,14-eicosatetraenoic acid |Common Name=&amp;&amp;5,12-Dihydr...</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBF20406HP08&amp;diff=55645&amp;oldid=prev"/>
		<updated>2010-10-27T06:45:56Z</updated>

		<summary type="html">&lt;p&gt;New page: {{Lipid/Header}}  {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |LipidBank=DFA8087 |LipidMaps=LMFA03060046 |SysName=5,12-Dihydroperoxy-6,8,10,14-eicosatetraenoic acid |Common Name=&amp;amp;&amp;amp;5,12-Dihydr...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Lipid/Header}}&lt;br /&gt;
&lt;br /&gt;
{{Hierarchy|{{PAGENAME}}}}&lt;br /&gt;
&lt;br /&gt;
{{Metabolite&lt;br /&gt;
|LipidBank=DFA8087&lt;br /&gt;
|LipidMaps=LMFA03060046&lt;br /&gt;
|SysName=5,12-Dihydroperoxy-6,8,10,14-eicosatetraenoic acid&lt;br /&gt;
|Common Name=&amp;amp;&amp;amp;5,12-Dihydroperoxy-6,8,10,14-eicosatetraenoic acid&amp;amp;&amp;amp;&lt;br /&gt;
|Mass Spectra=GC-EI-MS(Me-ester;after reduction, hydrogenation and TMS-derivatization)[[Reference:Yamagata_S:Murakami_H:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1983,47,2791|{{RelationTable/GetFirstAuthor|Reference:Yamagata_S:Murakami_H:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1983,47,2791}}]][[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587}}]]: m/e=487[M-CH3]; 401[M-(CH2)3COOCH3]; 389[M-(CH2)7CH3]; 311[401- HOTMS]; 299[389-HOTMS]; 215[SMTO=CH(CH2)7CH3]; 203[SMTO=CH(CH2)3COOCH3]&lt;br /&gt;
|UV Spectra=UV(Me-ester)[[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587}}]] conjugated triene: 270nm and 281nm&lt;br /&gt;
|IR Spectra=IR(Me-ester)[[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587}}]] OOH group: 3400cm^{-1}&lt;br /&gt;
|NMR Spectra=^1 H-NMR(Me-ester)[[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587}}]]OOH: 8.3ppm&lt;br /&gt;
|Source=Autooxidation of arachidonic acid[[Reference:Yamagata_S:Murakami_H:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1983,47,2791|{{RelationTable/GetFirstAuthor|Reference:Yamagata_S:Murakami_H:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1983,47,2791}}]]. In degradation products of 12-hydroperoxides of arachidonic acid in the presence of Fe(III)-ascorbic acid. Oxidation of arachidonic acid by singlet-oxygen[[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1981,45,587}}]]. It is produced enzymatically from 5- or 12-HPETE in vivo(5,12-DHPETE)&amp;lt;!--8103--&amp;gt;&amp;lt;!--8104--&amp;gt;.&lt;br /&gt;
|Chemical Synthesis=&lt;br /&gt;
|Metabolism=&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
{{Lipid/Footer}}&lt;/div&gt;</summary>
		<author><name>Editor</name></author>
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