LBF20503HO09: Difference between revisions

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{{Metabolite
{{Metabolite
|LipidBank=DFA8118
|LipidBank=DFA8118
|LipidMaps=LMFA03070001
|LipidMaps=-
|SysName=5S-Hydroxy- (6-trans,8-cis,11-cis,14-cis,17-cis) -icosapentaenoic acid
|SysName=5S-Hydroxy- (trans-6,cis-8,cis-11,cis-14,cis-17) -eicosapentaenoic acid
|Common Name=&&5S-Hydroxy- (6E,8Z,11Z,14Z,17Z) -eicosapentaenoic acid&&
|Common Name=&&5S-Hydroxy- (6E,8Z,11Z,14Z,17Z) -eicosapentaenoic acid&&5-HEPE&&
|UV Spectra= lambda max: 236nm  epsilon : 23,000
|UV Spectra= lambda max: 236nm  epsilon : 23,000
|Source=The synthesis of 5(S)-HEPE from EPA by tissue homogenates has been demonstrated [[Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349}}]][[Reference:Kulkarni_PS:Srinivasan_BD:,Prostaglandins,1986,31,1159|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Srinivasan_BD:,Prostaglandins,1986,31,1159}}]].
|Source=The synthesis of 5(S)-HEPE from EPA by tissue homogenates has been demonstrated [[Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Kaufman_PL:Srinivasan_BD:,J. Ocul. Pharmacol.,1987,3,349}}]][[Reference:Kulkarni_PS:Srinivasan_BD:,Prostaglandins,1986,31,1159|{{RelationTable/GetFirstAuthor|Reference:Kulkarni_PS:Srinivasan_BD:,Prostaglandins,1986,31,1159}}]].
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|Metabolism=
|Metabolism=
|Symbol=5(S)-HEPE
|Symbol=5(S)-HEPE
}}
{{MassbankSpectra|
UT000163
UT000164
UT000165
UT000166
UT000167
UT000168
UT000169
UT000170
UT000171
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 00:00, 17 January 2014

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Upper classes: LB LBF



5S-Hydroxy- (6E,8Z,11Z,14Z,17Z) -eicosapentaenoic acid
LBF20503HO09.png
Structural Information
5S-Hydroxy- (trans-6,cis-8,cis-11,cis-14,cis-17) -eicosapentaenoic acid
  • 5S-Hydroxy- (6E,8Z,11Z,14Z,17Z) -eicosapentaenoic acid
  • 5-HEPE
5(S)-HEPE
Formula C20H30O3
Exact Mass 318.21949482599996
Average Mass 318.4504
SMILES C(CC=CCC=CCC=CC=CC(CCCC(O)=O)O)=CCC
Physicochemical Information
The synthesis of 5(S)-HEPE from EPA by tissue homogenates has been demonstrated Kulkarni_PS et al. Kulkarni_PS 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. LBF20503HO09 See above. Kulkarni_PS et al. 1987
n.a. LBF20503HO09 See above. Kulkarni_PS et al. 1986