LBF20406LT13

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

Journals (雑誌一覧)

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Upper classes: LB LBF

IDs and Links
LipidBank	XPR3301
LipidMaps	LMFA03020006
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406LT13

LEUKOTRIENE D4
Structural Information
Systematic Name	5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
Common Name	LEUKOTRIENE D4 5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
Symbol
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
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility	METHANOL Morris_HR et al.
Source	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 .
Chemical Synthesis	Cohen_N et al.
Metabolism	g-Glutamyl transpeptidase hydrolyzes the glutathione moiety of leukotriene C4 and produces leukotriene D4 liberating glutamic acid Hammarstrom_S ,
Biological Activity
Genetic Information
Note
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	l MeOHmax = 270(e 32,000), 280(e 40,000), 290(e 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