LBF20306HO07: Difference between revisions

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|LipidMaps=-
|LipidMaps=-
|SysName= (R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid
|SysName= (R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid
|Common Name=&& (R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid&&
|Common Name=&&(R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid&&
|Reflactive=METHYL ESTER ; [<FONT FACE=""Symbol"">a</FONT>]X<sub>D</sub><sup>23</sup>=-3.0°(C=0.8, ACETONE) [[Reference:Shin_DS:Yadagiri_P:Falck_JR:Masferrer_JL:Schwartzman_ML:,Tetrah. Lett.,1989,30,3923|{{RelationTable/GetFirstAuthor|Reference:Shin_DS:Yadagiri_P:Falck_JR:Masferrer_JL:Schwartzman_ML:,Tetrah. Lett.,1989,30,3923}}]]
|Reflactive=METHYL ESTER ; [<FONT FACE=""Symbol"">a</FONT>]X<sub>D</sub><sup>23</sup>=-3.0°(C=0.8, ACETONE) [[Reference:Shin_DS:Yadagiri_P:Falck_JR:Masferrer_JL:Schwartzman_ML:,Tetrah. Lett.,1989,30,3923|{{RelationTable/GetFirstAuthor|Reference:Shin_DS:Yadagiri_P:Falck_JR:Masferrer_JL:Schwartzman_ML:,Tetrah. Lett.,1989,30,3923}}]]
|Solubility=ETHYL ACETATE [[Reference:Murphy_RC:Falck_JR:Lumin_S:Yadagiri_P:Zirrolli_JA:Balazy_M:Masferrer_JL:Abraham_NG:Schwartzman_ML:,J. Biol. Chem.,1988,263,17197|{{RelationTable/GetFirstAuthor|Reference:Murphy_RC:Falck_JR:Lumin_S:Yadagiri_P:Zirrolli_JA:Balazy_M:Masferrer_JL:Abraham_NG:Schwartzman_ML:,J. Biol. Chem.,1988,263,17197}}]]
|Solubility=ETHYL ACETATE [[Reference:Murphy_RC:Falck_JR:Lumin_S:Yadagiri_P:Zirrolli_JA:Balazy_M:Masferrer_JL:Abraham_NG:Schwartzman_ML:,J. Biol. Chem.,1988,263,17197|{{RelationTable/GetFirstAuthor|Reference:Murphy_RC:Falck_JR:Lumin_S:Yadagiri_P:Zirrolli_JA:Balazy_M:Masferrer_JL:Abraham_NG:Schwartzman_ML:,J. Biol. Chem.,1988,263,17197}}]]

Revision as of 00:02, 20 December 2008


Upper classes: LB LBF



(R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid
LBF20306HO07.png
Structural Information
(R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid
  • (R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid
Formula C20H34O3
Exact Mass 322.25079495399996
Average Mass 322.48216
SMILES C(CC=CC[C@H](CCC=CCC=CCCCC(O)=O)O)CCC
Physicochemical Information
ETHYL ACETATE Murphy_RC et al.
Spectral Information
Mass Spectra METHYL ESTER TMS ETHER ; m/e 393, 319, 297 Murphy_RC et al.
UV Spectra
IR Spectra
NMR Spectra METHYL ESTER ; 1H-NMR(CDCL3) : d 5.63-5.51(m, 1H), 5.47-5.28(m, 5H), 3.67(S, 3H), 3.67-3.57(m, 1H), 2.79(t, J=5.5Hz, 2H), 2.32(t, J=7.4Hz, 3H), 2.30-1.99(m, 6H), 1.76-1.39(m, 6H), 1.40-1.23(m, 6H), 0.88(t, J=6.8Hz, 3H) Shin_DS et al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20306HO07 See above. Murphy_RC et al. 1988
n.a. LBF20306HO07 See above. Shin_DS et al. 1989