LBF20407LX01

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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	DFA8153
LipidMaps	LMFA03040001
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20407LX01

lipoxin A4
Structural Information
Systematic Name	5S,6R,15S-trihydroxy-7E,9E,11Z,13E-eicosatetraenoic acid
Common Name	lipoxin A4 5S,6R,15S-trihydroxy-7E,9E,11Z,13E-eicosatetraenoic acid
Symbol	LXA4
Formula	C20H32O5
Exact Mass	352.224974134
Average Mass	352.46508
SMILES	C(CCC(C=CC=CC=CC=CC(O)C(O)CCCC(O)=O)O)CC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	LXA4 is formed in vitro by a number of mechanisms from arachidonic acid, 15-HpETE, and leukotriene A4 (LTA4 ) Edenius_C et al. Serhan_CN et al..
Chemical Synthesis
Metabolism
Biological Activity	LXA is equipotent to LTB in inducing superoxide generation in human neutrophils (0.1mM) Serhan_CN et al.. LXA4 is associated with several other biological functions including leukocyte activation, chemotaxis promotion, natural killer cell inhibition, and monocyte migration and adhesion Serhan_CN et al. Ramstedt_U et al. Maddox_JF et al..
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra	lmax: 302nm e: 50,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies ID Compound Name Reference Comment n.a. LBF20407LX01 See above. Adams_J et al. 1985 n.a. LBF20407LX01 See above. Brady_HR et al. 1996 n.a. LBF20407LX01 See above. Edenius_C et al. 1991 n.a. LBF20407LX01 See above. Fiore_S et al. 1994 n.a. LBF20407LX01 See above. Maddox_JF et al. 1996 n.a. LBF20407LX01 See above. Ramstedt_U et al. 1987 n.a. LBF20407LX01 See above. Serhan_CN 1994 n.a. LBF20407LX01 See above. Serhan_CN et al. 1984 n.a. LBF20407LX01 See above. Serhan_CN et al. 1984 n.a. LBF20407LX01 See above. Serhan_CN et al. 1986