LBF20306HO07: Difference between revisions

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Revision as of 06:00, 7 January 2010

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(脂肪酸)

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Upper classes: LB LBF

(R) , (Z,Z,Z) -12-Hydroxy-5,8,14-eicosatetraenoic acid

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



	METHYL ESTER ; [a]X_D²³=-3.0°(C=0.8, ACETONE) Shin_DS et al.

	ETHYL ACETATE Murphy_RC et al.
	The compound is produced from arachidonic acid which is incubated with bovine corneal microsomes in the presenc of NADPH Murphy_RC et al..
	Shin_DS et al.

	The compound has vasodilatory activity, and may be involved in the wound-healing of corneal injury 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

@@ Line 8: / Line 8: @@
 |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&&
-|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}}]]
+|Optical=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}}]]
 |Mass Spectra=METHYL ESTER TMS ETHER ; m/e 393, 319, 297 [[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}}]]
@@ Line 15: / Line 15: @@
 |Chemical Synthesis=[[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}}]] {{Image200|LBF20306HO07FT0001.gif}}
 |Metabolism=
+|Biological Activity=The compound has vasodilatory activity, and may be involved in the wound-healing of corneal injury [[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}}]].
 }}
 {{Lipid/Footer}}

IDs and Links
LipidBank	XPR6122
LipidMaps	-
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}

mol	LBF20306HO07

LBF20306HO07: Difference between revisions

Revision as of 06:00, 7 January 2010

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