LBF20406EO01: Difference between revisions

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|LipidBank=XPR6304
|LipidBank=XPR6304
|LipidMaps=-
|LipidMaps=-
|SysName=(5-cis,8-cis,11-cis,14-cis) -(17R,18S)-Epoxy-eicosatetraenoic acid
|SysName=(17R,18S) -Epoxy- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoic acid
|Common Name=&&17,18- (R,S) -Epoxy-5,8,11,14- (Z,Z,Z,Z) -eicosatetraenoic acid&&
|Common Name=&&(17R,18S) -Epoxy- (5Z,8Z,11Z,14Z) -eicosatetraenoic acid&&
|Mass Spectra=d,l-mixture, METHYL ESTER ; m/e 303, 301, 285, 275, 273, 271, 260, 257, 253, 245, 243, 231, 217, 213, 206, 199, 187, 180, 173, 159, 145, 131, 119, 117, 105, 93, 91(100%), 81, 79, 71, 67, 59, 57, 55 [[Reference:VanRollins_M:,Lipids,1990,25,481|{{RelationTable/GetFirstAuthor|Reference:VanRollins_M:,Lipids,1990,25,481}}]]
|Mass Spectra=d,l-mixture, METHYL ESTER ; m/e 303, 301, 285, 275, 273, 271, 260, 257, 253, 245, 243, 231, 217, 213, 206, 199, 187, 180, 173, 159, 145, 131, 119, 117, 105, 93, 91(100%), 81, 79, 71, 67, 59, 57, 55 [[Reference:VanRollins_M:,Lipids,1990,25,481|{{RelationTable/GetFirstAuthor|Reference:VanRollins_M:,Lipids,1990,25,481}}]]
|Source=The compound is produced when the microsomes of monkey seminal vesicle is incubated with 5,8,11,14,17-eicosapentaenoic acid [[Reference:Oliw_EH:,J. Biol. Chem.,1989,264,17845|{{RelationTable/GetFirstAuthor|Reference:Oliw_EH:,J. Biol. Chem.,1989,264,17845}}]].
|Source=The compound is produced when the microsomes of monkey seminal vesicle is incubated with 5,8,11,14,17-eicosapentaenoic acid [[Reference:Oliw_EH:,J. Biol. Chem.,1989,264,17845|{{RelationTable/GetFirstAuthor|Reference:Oliw_EH:,J. Biol. Chem.,1989,264,17845}}]].

Latest revision as of 06:18, 21 October 2010

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Upper classes: LB LBF



(17R,18S) -Epoxy- (5Z,8Z,11Z,14Z) -eicosatetraenoic acid
LBF20406EO01.png
Structural Information
(17R,18S) -Epoxy- (cis-5,cis-8,cis-11,cis-14) -eicosatetraenoic acid
  • (17R,18S) -Epoxy- (5Z,8Z,11Z,14Z) -eicosatetraenoic acid
17(18)EpETE
Formula C20H30O3
Exact Mass 318.21949482599996
Average Mass 318.4504
SMILES C(=CCC=CCCCC(O)=O)CC=CCC=CC[C@@H](O1)[C@@H]1CC
Physicochemical Information
The compound is produced when the microsomes of monkey seminal vesicle is incubated with 5,8,11,14,17-eicosapentaenoic acid Oliw_EH .
VanRollins_M
LBF20406EO01FT0001.gif
Spectral Information
Mass Spectra d,l-mixture, METHYL ESTER ; m/e 303, 301, 285, 275, 273, 271, 260, 257, 253, 245, 243, 231, 217, 213, 206, 199, 187, 180, 173, 159, 145, 131, 119, 117, 105, 93, 91(100%), 81, 79, 71, 67, 59, 57, 55 VanRollinsM
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406EO01 See above. Oliw_EH 1989
n.a. LBF20406EO01 See above. VanRollins_M 1990