LBF20406LT12: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidBank=XPR3121
|LipidBank=XPR3121
|LipidMaps=LMFA03020019
|LipidMaps=LMFA03020019
|SysName=5S,12R-dihydroxy-20,20,20-trifluoro-6Z,8E,10E,14Z-eicosatetraenoic acid
|SysName=(5S,12R) -Dihydroxy-20,20,20-trifluoro- (cis-6,trans-8,trans-10,cis-14) -eicosatetraenoic acid
|Common Name=&&20-trifluoro Leukotriene B4&&
|Common Name=&&20-trifluoro Leukotriene B_4&&(5S,12R) -Dihydroxy-20,20,20-trifluoro- (6Z,8E,10E,14Z) -eicosatetraenoic acid&&
|Source=
|Chemical Synthesis=
|Metabolism=
|Biological Activity=20-trifluoro LTB4 has equal chemotactic activity to LTB4 with an EC50 of 3 nM [[Reference:Tsai_BS:Keith_RH:Villani-Price_D:Haack_RA:Bauer_RF:Leonard_R:Abe_Y:Nicolaou_KC:,Prostaglandins,1989,37,287|{{RelationTable/GetFirstAuthor|Reference:Tsai_BS:Keith_RH:Villani-Price_D:Haack_RA:Bauer_RF:Leonard_R:Abe_Y:Nicolaou_KC:,Prostaglandins,1989,37,287}}]][[Reference:Nilsson_E:Gyllenhammar_H:Lerner_R:Palmblad_J:Ringertz_B:,Scand. J. Immunol.,1991,33,357|{{RelationTable/GetFirstAuthor|Reference:Nilsson_E:Gyllenhammar_H:Lerner_R:Palmblad_J:Ringertz_B:,Scand. J. Immunol.,1991,33,357}}]] but not degranulation activity of neutrophils.[[Reference:Tanaka_Y:Klauck_TM:Jubiz_W:Taguchi_T:Hanzawa_Y:Igarashi_A:Inazawa_K:Kobayashi_Y:Briggs_RG:,Arch. Biochem. Biophys.,1988,263,178|{{RelationTable/GetFirstAuthor|Reference:Tanaka_Y:Klauck_TM:Jubiz_W:Taguchi_T:Hanzawa_Y:Igarashi_A:Inazawa_K:Kobayashi_Y:Briggs_RG:,Arch. Biochem. Biophys.,1988,263,178}}]][[Reference:Tsai_BS:Keith_RH:Villani-Price_D:Haack_RA:Bauer_RF:Leonard_R:Abe_Y:Nicolaou_KC:,Prostaglandins,1989,37,287|{{RelationTable/GetFirstAuthor|Reference:Tsai_BS:Keith_RH:Villani-Price_D:Haack_RA:Bauer_RF:Leonard_R:Abe_Y:Nicolaou_KC:,Prostaglandins,1989,37,287}}]][[Reference:Nilsson_E:Gyllenhammar_H:Lerner_R:Palmblad_J:Ringertz_B:,Scand. J. Immunol.,1991,33,357|{{RelationTable/GetFirstAuthor|Reference:Nilsson_E:Gyllenhammar_H:Lerner_R:Palmblad_J:Ringertz_B:,Scand. J. Immunol.,1991,33,357}}]]
}}
}}
{{Lipid/Footer}}

Latest revision as of 07:53, 21 October 2010

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Upper classes: LB LBF



20-trifluoro Leukotriene B4
LBF20406LT12.png
Structural Information
(5S,12R) -Dihydroxy-20,20,20-trifluoro- (cis-6,trans-8,trans-10,cis-14) -eicosatetraenoic acid
  • 20-trifluoro Leukotriene B4
  • (5S,12R) -Dihydroxy-20,20,20-trifluoro- (6Z,8E,10E,14Z) -eicosatetraenoic acid
Formula C20H29F3O4
Exact Mass 390.201794016
Average Mass 390.4370696
SMILES C(F)(F)(F)CCCCC=CC[C@H](C=CC=CC=C[C@H](CCCC(O)=O)O)O
Physicochemical Information
20-trifluoro LTB4 has equal chemotactic activity to LTB4 with an EC50 of 3 nM Tsai_BS et al. Nilsson_E et al. but not degranulation activity of neutrophils. Tanaka_Y et al. Tsai_BS et al. Nilsson_E 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. LBF20406LT12 See above. Nilsson_E et al. 1991
n.a. LBF20406LT12 See above. Tanaka_Y et al. 1988
n.a. LBF20406LT12 See above. Tsai_BS et al. 1989