LBF20406LT11: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidBank=XPR3120
|LipidBank=XPR3120
|LipidMaps=LMFA03020018
|LipidMaps=LMFA03020018
|SysName=5S,12R,20-trihydroxy-6Z,8E,10E,14Z-eicosatetraenoic acid
|SysName=(5S,12R,20) -Trihydroxy- (cis-6,trans-8,trans-10,cis-14) -eicosatetraenoic acid
|Common Name=&&20-hydroxy Leukotriene B4&&5S,12R,20-trihydroxy-6Z,8E,10E,14Z-eicosatetraenoic acid&&
|Common Name=&&20-hydroxy Leukotriene B_4&&(5S,12R,20) -Trihydroxy- (6Z,8E,10E,14Z) -eicosatetraenoic acid&&20-hydroxy LTB4&&
|Source=
|Chemical Synthesis=
|Metabolism=
|Biological Activity=20-hydroxy LTB4 is commonly accepted as a inactive metabolite of LTB4 but reported to contract parenchymal strips from guinea pig lung [[Reference:Hansson_G:Lindgren_JA:Dahlen_SE:Hedqvist_P:Samuelsson_B:,FEBS Lett.,1981,130,107|{{RelationTable/GetFirstAuthor|Reference:Hansson_G:Lindgren_JA:Dahlen_SE:Hedqvist_P:Samuelsson_B:,FEBS Lett.,1981,130,107}}]] and as a good ligand form BLT2 receptor.[[Reference:Yokomizo_T:Kato_K:Hagiya_H:Izumi_T:Shimizu_T:,J. Biol. Chem.,2001,276,12454|{{RelationTable/GetFirstAuthor|Reference:Yokomizo_T:Kato_K:Hagiya_H:Izumi_T:Shimizu_T:,J. Biol. Chem.,2001,276,12454}}]]
}}
 
{{MassbankSpectra|
UT000289
UT000290
UT000291
UT000292
UT000293
UT000294
UT000295
UT000296
UT000297
}}
}}
{{Lipid/Footer}}

Latest revision as of 08:51, 5 April 2016

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Upper classes: LB LBF



20-hydroxy Leukotriene B4
LBF20406LT11.png
Structural Information
(5S,12R,20) -Trihydroxy- (cis-6,trans-8,trans-10,cis-14) -eicosatetraenoic acid
  • 20-hydroxy Leukotriene B4
  • (5S,12R,20) -Trihydroxy- (6Z,8E,10E,14Z) -eicosatetraenoic acid
  • 20-hydroxy LTB4
Formula C20H32O5
Exact Mass 352.224974134
Average Mass 352.46508
SMILES C(CCC=CC[C@H](C=CC=CC=C[C@H](CCCC(O)=O)O)O)CCO
Physicochemical Information
20-hydroxy LTB4 is commonly accepted as a inactive metabolite of LTB4 but reported to contract parenchymal strips from guinea pig lung Hansson_G et al. and as a good ligand form BLT2 receptor. Yokomizo_T et al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406LT11 See above. Hansson_G et al. 1981
n.a. LBF20406LT11 See above. Yokomizo_T et al. 2001