LBF20406LT13

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Upper classes: LB LBF



LEUKOTRIENE D4
LBF20406LT13.png
Structural Information
5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
  • LEUKOTRIENE D4
  • 5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
LTD4
Formula C25H40N2O6S
Exact Mass 496.260707712
Average Mass 496.66098
SMILES C(=CC=CC=C[C@@H](SC[C@@H](C(=O)NCC(O)=O)N)[C@H](CCCC(O)=O)O)CC=CCCCCC
Physicochemical Information
METHANOL Morris_HR et al.
Leukotriene D4 is produced by basophils, eosinophils and macrophages of various animal species upon various stimulations on the cells Samuelsson_B et al. Hammarstrom_S .
Cohen_N et al.
LBF20406LT13FT0001.gif
gamma -Glutamyl transpeptidase hydrolyzes the glutathione moiety of leukotriene C4 and produces leukotriene D4 liberating glutamic acid Hammarstrom_S ,
Leukotriene D4 stimulates airway smooth muscles and causes bronchoconstriction. Vascular permeability is enhanced. Gasstrointestinal smooth muscles are contracted Samuelsson_B et al. Hammarstrom_S . Leukotriene D4 binds to a receptor with 7 transmembrane domains coupled to Gi alpha /o protein (CysLT1) with an affinity higher by two orders of magnitude than that of leukotriene C4 Lynch_KR et al..
cDNA for CysLT1 was cloned Lynch_KR et al..
Spectral Information
Mass Spectra N-ACETYL, 5-TRIMETHYLSILYL ETHER DIMETHYL ESTER derivative ; 638(M+), 623, 607, 548, 508, 405, 404, 315, 314, 274, 273 Morris_HR et al.
UV Spectra λ MeOH
max
     = 270( ε 32,000), 280( ε 40,000), 290( ε 31,000)nm Lewis_RA et al.
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20406LT13 See above. Cohen_N et al. 1983
n.a. LBF20406LT13 See above. Hammarstrom_S 1983
n.a. LBF20406LT13 See above. Lewis_RA et al. 1980
n.a. LBF20406LT13 See above. Lynch_KR et al. 1999
n.a. LBF20406LT13 See above. Morris_HR et al. 1980
n.a. LBF20406LT13 See above. Samuelsson_B et al. 1982