LBF16306HO01: Difference between revisions
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|Common Name=&&8R-hydroxy-4Z,6E,10Z-hexadecatrienoic acid&& | |Common Name=&&8R-hydroxy-4Z,6E,10Z-hexadecatrienoic acid&& | ||
|UV Spectra=<FONT FACE="Symbol">l</FONT>max: 234nm <FONT FACE="Symbol">e</FONT>: 23,000 | |UV Spectra=<FONT FACE="Symbol">l</FONT>max: 234nm <FONT FACE="Symbol">e</FONT>: 23,000 | ||
|Source= | |||
|Chemical Synthesis= | |||
|Metabolism=Metabolism of 12(R)-HETE in corneal tissue produces predominantly the compound resulting from the loss of four carbon atoms through <FONT FACE="Symbol">b</FONT>-oxidation from C-1 [[Reference:Nishimura_M:Schwartzman_ML:Falck_JR:Lumin_S:Zirrolli_JA:Murphy_RC:,Arch. Biochem. Biophys.,1991,290,326|{{RelationTable/GetFirstAuthor|Reference:Nishimura_M:Schwartzman_ML:Falck_JR:Lumin_S:Zirrolli_JA:Murphy_RC:,Arch. Biochem. Biophys.,1991,290,326}}]];>. This metabolite is 8(R)-hydroxy hexadecatrienoic acid (8(R)-HHxTrE) or 2,3,4,5-tetranor 12(R)-HETE. | |||
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{{Lipid/Footer}} | {{Lipid/Footer}} |
Revision as of 07:00, 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 | |
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LipidBank | DFA8137 |
LipidMaps | LMFA01050143 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF16306HO01 |
8R-hydroxy-4Z,6E,10Z-hexadecatrienoic acid | |
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Structural Information | |
8R-hydroxy-4Z,6E,10Z-hexadecatrienoic acid | |
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Formula | C16H26O3 |
Exact Mass | 266.18819469799996 |
Average Mass | 266.37584 |
SMILES | CCCCCC=CCC(O)C=CC=CCCC(O)=O |
Physicochemical Information | |
Metabolism of 12(R)-HETE in corneal tissue produces predominantly the compound resulting from the loss of four carbon atoms through b-oxidation from C-1 Nishimura_M et al.;>. This metabolite is 8(R)-hydroxy hexadecatrienoic acid (8(R)-HHxTrE) or 2,3,4,5-tetranor 12(R)-HETE. | |
Spectral Information | |
Mass Spectra | |
UV Spectra | lmax: 234nm e: 23,000 |
IR Spectra | |
NMR Spectra | |
Other Spectra | |
Chromatograms |
[hide]Reported Metabolites, References | ||||||||||
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