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	<title>LBF22408AM05 - Revision history</title>
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	<updated>2026-04-30T21:48:53Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://lipidbank.jp/mediawiki/index.php?title=LBF22408AM05&amp;diff=56787&amp;oldid=prev</id>
		<title>Editor: New page: {{Lipid/Header}}  {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |LipidBank=XPR7060 |LipidMaps=LMFA08020046 |SysName=N-Propyl-16,16-dimethyl- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylamine |...</title>
		<link rel="alternate" type="text/html" href="https://lipidbank.jp/mediawiki/index.php?title=LBF22408AM05&amp;diff=56787&amp;oldid=prev"/>
		<updated>2010-10-22T07:19:44Z</updated>

		<summary type="html">&lt;p&gt;New page: {{Lipid/Header}}  {{Hierarchy|{{PAGENAME}}}}  {{Metabolite |LipidBank=XPR7060 |LipidMaps=LMFA08020046 |SysName=N-Propyl-16,16-dimethyl- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylamine |...&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=XPR7060&lt;br /&gt;
|LipidMaps=LMFA08020046&lt;br /&gt;
|SysName=N-Propyl-16,16-dimethyl- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylamine&lt;br /&gt;
|Common Name=&amp;amp;&amp;amp;N-Propyl-16,16-dimethyl- (5Z,8Z,11Z,14Z) -docosatetraenoylamine&amp;amp;&amp;amp;16,16-Dimethyldocosa- (5Z,8Z,11Z,14Z) -tetraenoylpropylamine&amp;amp;&amp;amp;&lt;br /&gt;
|NMR Spectra=^1 H NMR (CDCl3)  delta 5.36 (overlap m, 7H, NH, 5,6,8,9,11,12-vinyl-H), 5.21 (m, 2H, 14,15-vinyl-H), 3.21 (q, 2H, J=6.7Hz, N-CH2), 2.92 (t, 2H, J=5.9Hz, 13-CH2), 2.80 (m, 4H, 7,10-CH2), 2.16,2.12 (t, m, 4H, J=7.6Hz, 2&amp;amp;4-CH2), 1.71 (p, 2H, J=7.4Hz, 3-CH2), 1.52 (hx, 2H, J=7.3Hz, 2&amp;#039;-CH2), 1.25 (m, 10H, 17-21-CH2), 1.08 (s, 6H, gem-Me2), 0.91,0.87 (t,m, 6H, 3&amp;#039;-CH3, 22-CH3) [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]&lt;br /&gt;
|Source=&lt;br /&gt;
|Chemical Synthesis=Heating a methanolic solution of the corresponding ester, NaCN and n-propylamine for 2days in a hot block at 50°C.Yield 44%. [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]&lt;br /&gt;
|Metabolism=&lt;br /&gt;
|Biological Activity={{Image200|LBF20408AM05FT7060.gif}} [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
{{Lipid/Footer}}&lt;/div&gt;</summary>
		<author><name>Editor</name></author>
	</entry>
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