http://metabolomics.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20306CV01
LBF20306CV01 - Revision history
2026-05-04T10:21:12Z
Revision history for this page on the wiki
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http://metabolomics.jp/mediawiki/index.php?title=LBF20306CV01&diff=107253&oldid=prev
Editor at 00:00, 1 October 2008
2008-10-01T00:00:00Z
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<td colspan='2' style="background-color: white; color:black;">← Older revision</td>
<td colspan='2' style="background-color: white; color:black;">Revision as of 00:00, 1 October 2008</td>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>{{Metabolite</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>{{Metabolite</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>|LipidBank=XPR8040</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>|LipidBank=XPR8040</div></td></tr>
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http://metabolomics.jp/mediawiki/index.php?title=LBF20306CV01&diff=107252&oldid=prev
Editor at 00:00, 30 September 2008
2008-09-30T00:00:00Z
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<p><b>New page</b></p><div>{{Metabolite<br />
|LipidBank=XPR8040<br />
|LipidMaps=LMFA03120021<br />
|SysName= (R) -4-{ (Z) -3- [ (1R,2S) -2- [ (Z) -2-octenyl ] -5-oxo-3-cyclopentenyl ] -1-propenyl}-4-butanolide<br />
|Common Name=&&preclavulone lactone I <<8041>>&&<br />
|Reflactive=[<FONT FACE="Symbol">a</FONT>]<SUB><FONT SIZE=-1>D</FONT></SUB> -168.0°<<8041>><br />
|Mass Spectra=HRFABMS m/z 316.2028 for C<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>0</FONT></SUB>H<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>8</FONT></SUB>O<SUB><FONT SIZE=-1>3</FONT></SUB> (M<SUP><FONT SIZE=-1>+</FONT></SUP>), calcd 316.2038.<<8041>><br />
|UV Spectra=<FONT FACE="Symbol">l</FONT><SUP><FONT SIZE=-1>C</FONT></SUP><SUP><FONT SIZE=-1>H</FONT></SUP><SUP><FONT SIZE=-1>3</FONT></SUP><SUP><FONT SIZE=-1>C</FONT></SUP><SUP><FONT SIZE=-1>N</FONT></SUP>&<SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> 215 nm(<FONT FACE="Symbol">e</FONT>5740)<<8041>><br />
|IR Spectra=<FONT FACE="Symbol">n</FONT> 1775 and 1706cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP><<8041>><br />
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(500MHz,CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<FONT FACE="Symbol">d</FONT>ppm0.89(3H,t,J=7.5Hz),1.2-1.4(6H,m),1.92(1H,dtd,8.4,9.7,12.9Hz),2.01(2H,brq,J=7.3Hz),2.11(1H,dt,J=2.3,5.9),2.27(1H,brtd,J=7.0,14.5Hz),2.32(1H,brtd,J=7.1,14.5Hz),2.41(1H,qd,J=6.6,12.9Hz),2.52(2H,m),2.57(2H,dd,J=6.6,9.7Hz),2.72(1H,qt,J=2.3,7.0Hz),5.27(1H,dt,J=6.6,8.4Hz),5.36(1H,brtd,J=7.1,10.8Hz),5.53(1H,dd,J=8.4,11.1Hz),5.54(1H,m),5.56(1H,td,J=7.2,11.1Hz),6.16(1H,dd,J=2.3,5.1Hz),7.60(1H,dd,J=2.3,5.8Hz).<<8041>> <SUP><FONT SIZE=-1>1</FONT></SUP><SUP><FONT SIZE=-1>3</FONT></SUP>C-NMR(125MHz,CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<FONT FACE="Symbol">d</FONT>ppm14.0,22.5,27.3,27.5,28.9,29.1,29.2,31.3,31.5,46.3,50.3,76.0,125.2,129.9,130.9,133.1,133.4,167.2,177.0,210.6<<8041>><br />
}}</div>
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