LBF20207PG02: Difference between revisions

No edit summary
No edit summary
 
(12 intermediate revisions by the same user not shown)
Line 1: Line 1:
{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
{{Hierarchy|{{PAGENAME}}}}
{{Lipid/Header}}


{{Metabolite
{{Metabolite
|LipidBank=XPR1100
|LipidBank=XPR1100
|LipidMaps=LMFA03010131
|LipidMaps=LMFA03010131
|SysName=7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-1-cyclopenten-1-yl ] heptanoic acid / (E,S) -15-Hydroxy-9-oxo-8 (12) ,13-prostadienoic acid
|SysName=7- [2- (3S -Hydroxy-trans-1-octenyl) -5-oxo-3-cyclopenten-1 -yl] heptanoic acid
|Common Name=&&PROSTAGLANDIN B_1&&7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-1-cyclopenten-1-yl ] heptanoic acid&&(E,S) -15-Hydroxy-9-oxo-8 (12) ,13-prostadienoic acid&&
|Common Name=&&Prostaglandin B_1&&(E,S) -15-Hydroxy-9-oxo-8 (12) ,13-prostadienoic acid&&7- [ 2- (3S -Hydroxy-1(E)-octenyl) -5-oxo-3-cyclopenten-1 -yl ] heptanoic acid&&
|Melting Point=70-71°C [[Reference:Ramwell_PW:Shaw_JE:Clarke_GB:Grostic_MF:Kaiser_DG:Pike_JE:,Progr. Chem. Fats Other Lipids,1971,9,231|{{RelationTable/GetFirstAuthor|Reference:Ramwell_PW:Shaw_JE:Clarke_GB:Grostic_MF:Kaiser_DG:Pike_JE:,Progr. Chem. Fats Other Lipids,1971,9,231}}]]
|Melting Point=70-71°C [[Reference:Ramwell_PW:Shaw_JE:Clarke_GB:Grostic_MF:Kaiser_DG:Pike_JE:,Progr. Chem. Fats Other Lipids,1971,9,231|{{RelationTable/GetFirstAuthor|Reference:Ramwell_PW:Shaw_JE:Clarke_GB:Grostic_MF:Kaiser_DG:Pike_JE:,Progr. Chem. Fats Other Lipids,1971,9,231}}]]
|Mass Spectra=METHYL ESTER ; m/e 350(M<SUP><FONT SIZE=-1>+</FONT></SUP>), 332, 319, 301, 251, 219 [[Reference:Struijk_MCB:Beerthuis_RK:Pabon_HJJ:Van_Dorp_DA:,Recueil Travaux Quimiq Pays Bas,1966,85,1233|{{RelationTable/GetFirstAuthor|Reference:Struijk_MCB:Beerthuis_RK:Pabon_HJJ:Van_Dorp_DA:,Recueil Travaux Quimiq Pays Bas,1966,85,1233}}]]
|Mass Spectra=METHYL ESTER ; m/e 350(M^+ ), 332, 319, 301, 251, 219 [[Reference:Struijk_MCB:Beerthuis_RK:Pabon_HJJ:Van_Dorp_DA:,Recueil Travaux Quimiq Pays Bas,1966,85,1233|{{RelationTable/GetFirstAuthor|Reference:Struijk_MCB:Beerthuis_RK:Pabon_HJJ:Van_Dorp_DA:,Recueil Travaux Quimiq Pays Bas,1966,85,1233}}]]
|UV Spectra=<FONT FACE="Symbol">l</FONT> <SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> = 278nm(<FONT FACE="Symbol">e</FONT> 28,650) [[Reference:Jones_RL:,J. Lipid Res.,1972,13,511|{{RelationTable/GetFirstAuthor|Reference:Jones_RL:,J. Lipid Res.,1972,13,511}}]]
|UV Spectra= lambda  _{max} = 278nm( epsilon  28,650) [[Reference:Jones_RL:,J. Lipid Res.,1972,13,511|{{RelationTable/GetFirstAuthor|Reference:Jones_RL:,J. Lipid Res.,1972,13,511}}]]
|IR Spectra=5.91, 6.10, 6.27, 10.3<FONT FACE="Symbol">m</FONT>m [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|IR Spectra=5.91, 6.10, 6.27, 10.3 mu m [[Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Samuelsson_B:,J. Biol. Chem.,1966,241,257}}]]
|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR :<FONT FACE="Symbol">d</FONT> 6.87(d, J=16Hz, 1H, 13-CH), 6.25(d,d, J=16.6Hz, 1H, 14-CH), 4.38(1H, 15-CH) [[Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839|{{RelationTable/GetFirstAuthor|Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839}}]]
|NMR Spectra=^1 H-NMR : delta  6.87(d, J=16Hz, 1H, 13-CH), 6.25(d,d, J=16.6Hz, 1H, 14-CH), 4.38(1H, 15-CH) [[Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839|{{RelationTable/GetFirstAuthor|Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839}}]]
|Source=Prostaglandin B1 is found in human seminal plasma [[Reference:Bergstrom_S:,Science,1967,157,382|{{RelationTable/GetFirstAuthor|Reference:Bergstrom_S:,Science,1967,157,382}}]].
|Chemical Synthesis=[[Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839|{{RelationTable/GetFirstAuthor|Reference:Collins_P:Jung_CJ:Pappo_R:,Isr. J. Chem.,1968,6,839}}]] {{Image200|LBF20207PG02FT0001.gif}}
|Metabolism=
|Symbol=PGB1
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 08:27, 21 October 2010

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)


Upper classes: LB LBF



IDs and Links
LipidBank XPR1100
LipidMaps LMFA03010131
CAS
KEGG {{{KEGG}}}
KNApSAcK {{{KNApSAcK}}}
mol LBF20207PG02
Prostaglandin B1
LBF20207PG02.png
Structural Information
7- [2- (3S -Hydroxy-trans-1-octenyl) -5-oxo-3-cyclopenten-1 -yl] heptanoic acid
  • Prostaglandin B1
  • (E,S) -15-Hydroxy-9-oxo-8 (12) ,13-prostadienoic acid
  • 7- [ 2- (3S -Hydroxy-1(E)-octenyl) -5-oxo-3-cyclopenten-1 -yl ] heptanoic acid
 PGB1
Formula C20H32O4
Exact Mass 336.23005951199997
Average Mass 336.46567999999996
SMILES C(CC[C@@H](O)C=CC(=C1CCCCCCC(O)=O)CCC(=O)1)CC
Physicochemical Information
70-71°C Ramwell_PW et al.
Prostaglandin B1 is found in human seminal plasma Bergstrom_S .
Collins_P et al.
LBF20207PG02FT0001.gif
Spectral Information
Mass Spectra METHYL ESTER ; m/e 350(M+), 332, 319, 301, 251, 219 Struijk_MCB et al.
UV Spectra λ max = 278nm( ε 28,650) Jones_RL
IR Spectra 5.91, 6.10, 6.27, 10.3 μ m HambergMet al.
NMR Spectra 1H-NMR : δ 6.87(d, J=16Hz, 1H, 13-CH), 6.25(d,d, J=16.6Hz, 1H, 14-CH), 4.38(1H, 15-CH) CollinsPet al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20207PG02 See above. Bergstrom_S 1967
n.a. LBF20207PG02 See above. Collins_P et al. 1968
n.a. LBF20207PG02 See above. Hamberg_M et al. 1966
n.a. LBF20207PG02 See above. Jones_RL 1972
n.a. LBF20207PG02 See above. Ramwell_PW et al. 1971
n.a. LBF20207PG02 See above. Struijk_MCB et al. 1966


Retrieved from "http://lipidbank.jp/mediawiki/index.php?title=LBF20207PG02&oldid=52388"