LBF20306HX04: Difference between revisions
m (LBF20406HX02 moved to LBF20306HX04) |
m (LBF20406HX02 moved to LBF20306HX04) |
||
Line 14: | Line 14: | ||
|NMR Spectra=ACETATE METHYL ESTER ; <SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(C<SUB><FONT SIZE=-1>6</FONT></SUB>D<SUB><FONT SIZE=-1>6</FONT></SUB>) : <FONT FACE="Symbol">d</FONT> 5.67(dd, J=9.2, 6.4Hz, 1H, 10-CH), 5.52, 5.46, 5.42, 5.35, 5.32, 3.36(s, 3H, OCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 2.95(m, 2H, 7-CH), 2.92(m, 1H, 11-CH), 2.86(ddd, J=7.4, 7.4, 2.1Hz, 1H, 12-CH), 2.30(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.18(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.12(t, J=7.4Hz, 2H, 2-CH), 1.98(dt, J=7.4, 7.4Hz, 2H, 4-CH), 1.92(dt, J=8.8, 8.8Hz, 2H, 16-CH), 1.65(s, 3H, COCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 1.60(tt, J=7.4, 7.4Hz, 2H, 3-CH), 1.25(m, 6H), 0.88(t, J=7.0Hz, 3H, 20-CH). [[Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126|{{RelationTable/GetFirstAuthor|Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126}}]] <SUP><FONT SIZE=-1>1</FONT></SUP><SUP><FONT SIZE=-1>3</FONT></SUP>NMR(C<SUB><FONT SIZE=-1>6</FONT></SUB>D<SUB><FONT SIZE=-1>6</FONT></SUB>) : 134.22, 133.35, 130.17, 127.74, 124.31, 123.37, 70.86, 58.30, 55.71, 50.94, 33.30, 31.71, 29.66, 29.52, 27.59, 26.73, 25.00, 22.88, 20.53, 14.23 [[Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126|{{RelationTable/GetFirstAuthor|Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126}}]] | |NMR Spectra=ACETATE METHYL ESTER ; <SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(C<SUB><FONT SIZE=-1>6</FONT></SUB>D<SUB><FONT SIZE=-1>6</FONT></SUB>) : <FONT FACE="Symbol">d</FONT> 5.67(dd, J=9.2, 6.4Hz, 1H, 10-CH), 5.52, 5.46, 5.42, 5.35, 5.32, 3.36(s, 3H, OCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 2.95(m, 2H, 7-CH), 2.92(m, 1H, 11-CH), 2.86(ddd, J=7.4, 7.4, 2.1Hz, 1H, 12-CH), 2.30(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.18(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.12(t, J=7.4Hz, 2H, 2-CH), 1.98(dt, J=7.4, 7.4Hz, 2H, 4-CH), 1.92(dt, J=8.8, 8.8Hz, 2H, 16-CH), 1.65(s, 3H, COCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 1.60(tt, J=7.4, 7.4Hz, 2H, 3-CH), 1.25(m, 6H), 0.88(t, J=7.0Hz, 3H, 20-CH). [[Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126|{{RelationTable/GetFirstAuthor|Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126}}]] <SUP><FONT SIZE=-1>1</FONT></SUP><SUP><FONT SIZE=-1>3</FONT></SUP>NMR(C<SUB><FONT SIZE=-1>6</FONT></SUB>D<SUB><FONT SIZE=-1>6</FONT></SUB>) : 134.22, 133.35, 130.17, 127.74, 124.31, 123.37, 70.86, 58.30, 55.71, 50.94, 33.30, 31.71, 29.66, 29.52, 27.59, 26.73, 25.00, 22.88, 20.53, 14.23 [[Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126|{{RelationTable/GetFirstAuthor|Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126}}]] | ||
|Source=Hepoxilin B3 together with hepoxilin A3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]];>. | |Source=Hepoxilin B3 together with hepoxilin A3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]];>. | ||
|Chemical Synthesis= {{Image200| | |Chemical Synthesis= {{Image200|LBF20306HX04FT0001.gif}} | ||
|Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]];>. | |Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]];>. | ||
}} | }} | ||
{{Lipid/Footer}} | {{Lipid/Footer}} |
Revision as of 10:00, 25 November 2009
LipidBank Top (トップ) |
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) |
How to edit (ページの書き方) |
IDs and Links | |
---|---|
LipidBank | XPR5101 |
LipidMaps | LMFA03090003 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20306HX04 |
HEPOXILIN B3 | |
---|---|
Structural Information | |
10-Hydroxy-11 (R) ,12 (S) -epoxyeicosa-5,8,14 (Z,Z,Z) -trienoic acid | |
| |
Formula | C20H32O4 |
Exact Mass | 336.23005951199997 |
Average Mass | 336.46567999999996 |
SMILES | C(CC=CC[C@@H]([C@@H](C(O)C=CCC=CCCCC(O)=O)1)O1)CCC |
Physicochemical Information | |
DIETHYL ETHER Pace-Asciak_CR et al. | |
Hepoxilin B3 together with hepoxilin A3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin Pace-Asciak_CR ;>. | |
The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production Pace-Asciak_CR et al.;>. | |
Spectral Information | |
Mass Spectra | METHYL ESTER TMS ETHER ; m/e 311, 282, 269(base peak) Moghaddam_MF et al. |
UV Spectra | |
IR Spectra | ACETATE METHYL ESTER ; n(CHLOROFORM) 2956, 1743, 1550, 1372, 1234, 1033, 999cm-1 Moghaddam_MF et al. |
NMR Spectra | ACETATE METHYL ESTER ; 1H-NMR(C6D6) : d 5.67(dd, J=9.2, 6.4Hz, 1H, 10-CH), 5.52, 5.46, 5.42, 5.35, 5.32, 3.36(s, 3H, OCH3), 2.95(m, 2H, 7-CH), 2.92(m, 1H, 11-CH), 2.86(ddd, J=7.4, 7.4, 2.1Hz, 1H, 12-CH), 2.30(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.18(ddd, J=14.8, 7.4, 7.4Hz, 1H, 13-CH), 2.12(t, J=7.4Hz, 2H, 2-CH), 1.98(dt, J=7.4, 7.4Hz, 2H, 4-CH), 1.92(dt, J=8.8, 8.8Hz, 2H, 16-CH), 1.65(s, 3H, COCH3), 1.60(tt, J=7.4, 7.4Hz, 2H, 3-CH), 1.25(m, 6H), 0.88(t, J=7.0Hz, 3H, 20-CH). Moghaddam_MF et al. 13NMR(C6D6) : 134.22, 133.35, 130.17, 127.74, 124.31, 123.37, 70.86, 58.30, 55.71, 50.94, 33.30, 31.71, 29.66, 29.52, 27.59, 26.73, 25.00, 22.88, 20.53, 14.23 Moghaddam_MF et al. |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | ||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|