LBF20406OX02

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Fatty acid (脂肪酸)

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Upper classes: LB LBF

IDs and Links
LipidBank	DFA8157
LipidMaps	LMFA03060019
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406OX02

12-Oxo- (5Z,8Z,10E,14Z) -eicosatetraenoic acid
Structural Information
Systematic Name	12-Oxo- (cis-5,cis-8,trans-10,cis-14) -eicosatetraenoic acid
Common Name	12-Oxo- (5Z,8Z,10E,14Z) -eicosatetraenoic acid
Symbol	12-OxoETE/12-KETE
Formula	C20H30O3
Exact Mass	318.21949482599996
Average Mass	318.4504
SMILES	C(CC=CCC(C=CC=CCC=CCCCC(O)=O)=O)CCC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	12-OxoETE is synthesized by human platelets and Aplaysia nervous tissue after incubation with arachidonic acid Falgueyret_JP et al. Fruteau_de_Laclos_B et al.. Microsomal fractions of various tissues will reduce 12-oxoETE to 12(S)-HETE or a mixture of 12(S)- and 12(R)-HETE Falgueyret_JP et al. Falgueyret_JP et al..
Chemical Synthesis
Metabolism
Biological Activity	12-OxoETE induces a rapid, dose related increase of cytoplasmic free calcium via a leukotriene B4 receptor or a common activation sequence Naccache_PH et al..
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra	λ max: 280nm ε : 30,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406OX02 See above. Falgueyret_JP et al. 1990 n.a. LBF20406OX02 See above. Falgueyret_JP et al. 1988 n.a. LBF20406OX02 See above. Fruteau_de_Laclos_B et al. 1987 n.a. LBF20406OX02 See above. Naccache_PH et al. 1991