LBF20406LT01

Upper classes: LB LBF

IDs and Links
LipidBank	XPR3001
LipidMaps	LMFA03020023
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406LT01

LEUKOTRIENE A4
Structural Information
Systematic Name	5 (S) ,6 (S) -Epoxyeicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
Common Name	LEUKOTRIENE A4 5 (S) ,6 (S) -Epoxyeicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
Symbol
Formula	C20H30O3
Exact Mass	318.21949482599996
Average Mass	318.4504
SMILES	C(CC=CCC=CC=CC=C[C@@H](O1)[C@@H]1CCCC(O)=O)CCC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility	SOL. IN CYCLOHEXANE,METHANOL Corey_EJ et al.. STABILITIES : to decompose to 5,12-DIHYDROXY-6,8,10,14-EICOSATETRAENOIC ACID and 5,6-DIHYDROXY-7,9,11,14-EICOSATETRAENOIC ACID under neutral aqueous solution at 37°C with one minite of half-life BorgeatPet al..
Source
Chemical Synthesis
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra	METHYL ESTER ; 332(M+), 316, 300, 221, 189, 181, 129, 101 Mckay_SW et al.
UV Spectra	METHYL ESTER ; l MeOHmax = 269(e 30,500), 278(e 40,000), 287(e 34,400) nm Corey_EJ et al.
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies ID Compound Name Reference Comment n.a. LBF20406LT01 See above. Borgeat_P et al. 1979 n.a. LBF20406LT01 See above. Corey_EJ et al. 1979 n.a. LBF20406LT01 See above. Corey_EJ et al. 1980 n.a. LBF20406LT01 See above. Ford-Hutchinson_AW et al. 1994 n.a. LBF20406LT01 See above. Funk_CD 1993 n.a. LBF20406LT01 See above. Hammarstrom_S 1983 n.a. LBF20406LT01 See above. Mckay_SW et al. 1981 n.a. LBF20406LT01 See above. Samuelsson_B et al. 1982