LBF20503HO08: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
{{Hierarchy|{{PAGENAME}}}}


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|LipidBank=DFA8126
|LipidBank=DFA8126
|LipidMaps=LMFA03070009
|LipidMaps=LMFA03070009
|SysName=15S-hydroxy-5Z,8Z,11Z,13E,17Z-eicosapentaenoic acid
|SysName=15S-Hydroxy- (cis-5,cis-8,cis-11,trans-13,cis-17) -eicosapentaenoic acid
|Common Name=&&15S-hydroxy-5Z,8Z,11Z,13E,17Z-eicosapentaenoic acid&&
|Common Name=&&15S-Hydroxy- (5Z,8Z,11Z,13E,17Z) -eicosapentaenoic acid&&15-HEPE&&
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 236nm <FONT FACE="Symbol">e</FONT>: 23,000
|UV Spectra= lambda max: 236nm  epsilon : 23,000
|Source=The biosynthesis of 15-HEPE from EPA in guinea pig epidermal enzyme preparations has been documented [[Reference:Miller_C:Yamaguchi_RY:Ziboh_VA:,Lipids,1989,24,998|{{RelationTable/GetFirstAuthor|Reference:Miller_C:Yamaguchi_RY:Ziboh_VA:,Lipids,1989,24,998}}]].
|Chemical Synthesis=
|Metabolism=
|Symbol=15(S)-HEPE
|Biological Activity=15(S)-HEPE generated by soybean lipoxygenation of EPA inhibits RBL-1 cell 5-lipoxygenase with an IC_{50} of 28 mM[[Reference:Miller_C:Yamaguchi_RY:Ziboh_VA:,Lipids,1989,24,998|{{RelationTable/GetFirstAuthor|Reference:Miller_C:Yamaguchi_RY:Ziboh_VA:,Lipids,1989,24,998}}]].
}}
 
{{MassbankSpectra|
UT000100
UT000101
UT000102
UT000103
UT000104
UT000105
UT000106
UT000107
UT000108
}}
}}
{{Lipid/Footer}}

Latest revision as of 00:00, 17 January 2014

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Upper classes: LB LBF



15S-Hydroxy- (5Z,8Z,11Z,13E,17Z) -eicosapentaenoic acid
LBF20503HO08.png
Structural Information
15S-Hydroxy- (cis-5,cis-8,cis-11,trans-13,cis-17) -eicosapentaenoic acid
  • 15S-Hydroxy- (5Z,8Z,11Z,13E,17Z) -eicosapentaenoic acid
  • 15-HEPE
15(S)-HEPE
Formula C20H30O3
Exact Mass 318.21949482599996
Average Mass 318.4504
SMILES C(=CCC(C=CC=CCC=CCC=CCCCC(O)=O)O)CC
Physicochemical Information
The biosynthesis of 15-HEPE from EPA in guinea pig epidermal enzyme preparations has been documented Miller_C et al..
15(S)-HEPE generated by soybean lipoxygenation of EPA inhibits RBL-1 cell 5-lipoxygenase with an IC_{50} of 28 mM Miller_C et al..
Spectral Information
Mass Spectra
UV Spectra λ max: 236nm ε : 23,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20503HO08 See above. Miller_C et al. 1989