LBF20406LT05: Difference between revisions

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|LipidMaps=LMFA03020012
|LipidMaps=LMFA03020012
|SysName=N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6-cis,8-trans,10-trans,14-cis) -icosatetraenamide
|SysName=N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6-cis,8-trans,10-trans,14-cis) -icosatetraenamide
|Common Name=&&Leukotriene B4 Ethanolamide&&N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&
|Common Name=&&Leukotriene B_4 ethanolamide&&N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&
|Source=
|Source=
|Chemical Synthesis=
|Chemical Synthesis=

Revision as of 00:39, 2 June 2010

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Upper classes: LB LBF



Leukotriene B4ethanolamide
LBF20406LT05.png
Structural Information
N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6-cis,8-trans,10-trans,14-cis) -icosatetraenamide
  • Leukotriene B4ethanolamide
  • N- (2-Hydroxyethyl) - (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide
Formula C22H37NO4
Exact Mass 379.27225867699997
Average Mass 379.53352
SMILES C(=CC[C@@H](O)C=CC=CC=C[C@H](CCCC(=O)NCCO)O)CCCCC
Physicochemical Information
LTB4-EA is reported as a potent antagonist about 3 fold higher affinity for the human LTB4 receptor that LTB4. And LTB4-EA antagonizes the LTB4-induced contractions of guinea pig lung parenchyma with 10 nM as an EC50.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406LT05 See above. McHugh_D et al. 2003