LBF20306EO03

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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	DFA8112
LipidMaps	LMFA03080004
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20306EO03

(+-) -11 (12) -Epoxy- (5Z,8Z,14Z) -eicosatrienoic acid
Structural Information
Systematic Name	dl-11 (12) -Epoxy- (cis-5,cis-8,cis-14) -eicosatrienoic acid
Common Name	(+-) -11 (12) -Epoxy- (5Z,8Z,14Z) -eicosatrienoic acid 11,12-EET
Symbol	(+-)11(12)-EpETrE
Formula	C20H32O3
Exact Mass	320.23514489
Average Mass	320.46628
SMILES	C(CC=CCC(O1)C1CC=CCC=CCCCC(O)=O)CCC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	(±)11(12)-EpETrE is biosynthesized in rat and rabbit liver microsomes by cytochrome P450 Oliw_EH et al. Chacos_N et al..
Chemical Synthesis
Metabolism
Biological Activity	(±)11(12)-EpETrE has been shown, along with (±)8(9)-EpETrE, to play a role in the recovery of depleted Ca^{2+} pools in cultured smooth muscle cells Graber_MN et al..
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20306EO03 See above. Chacos_N et al. 1982 n.a. LBF20306EO03 See above. Falck_JR et al. 1984 n.a. LBF20306EO03 See above. Fitzpatrick_FA et al. 1988 n.a. LBF20306EO03 See above. Graber_MN et al. 1997 n.a. LBF20306EO03 See above. Mosset_P et al. 1986 n.a. LBF20306EO03 See above. Oliw_EH et al. 1982