LBF20406LT13: Difference between revisions

Revision as of 22:00, 26 July 2009

Upper classes: LB LBF

LEUKOTRIENE D4

Structural Information
	5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid
	LEUKOTRIENE D4 5 (S) -Hydroxy-6 (R) -S-cysteinylglycinyleicosa-7 (E) ,9 (E) ,11 (Z) ,14 (Z) -tetraenoic acid

Formula	C25H40N2O6S
Exact Mass	496.260707712
Average Mass	496.66098
SMILES	`C(=CC=CC=C[C@@H](SC[C@@H](C(=O)NCC(O)=O)N)[C@H](CCCC(O)=O)O)CC=CCCCCC`
Physicochemical Information





	METHANOL Morris_HR et al.






Spectral Information
Mass Spectra	N-ACETYL, 5-TRIMETHYLSILYL ETHER DIMETHYL ESTER derivative ; 638(M⁺), 623, 607, 548, 508, 405, 404, 315, 314, 274, 273 Morris_HR et al.
UV Spectra	l ^M^e^O^H_m_a_x = 270(e 32,000), 280(e 40,000), 290(e 31,000)nm Lewis_RA et al.
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies	ID	Compound Name	Reference
n.a.	LBF20406LT13	See above.	Cohen_N et al. 1983
n.a.	LBF20406LT13	See above.	Hammarstrom_S 1983
n.a.	LBF20406LT13	See above.	Lewis_RA et al. 1980
n.a.	LBF20406LT13	See above.	Lynch_KR et al. 1999
n.a.	LBF20406LT13	See above.	Morris_HR et al. 1980
n.a.	LBF20406LT13	See above.	Samuelsson_B et al. 1982

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 |UV Spectra=<FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>M</FONT></SUP><SUP><FONT SIZE=-1>e</FONT></SUP><SUP><FONT SIZE=-1>O</FONT></SUP><SUP><FONT SIZE=-1>H</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> = 270(<FONT FACE="Symbol">e</FONT> 32,000), 280(<FONT FACE="Symbol">e</FONT> 40,000), 290(<FONT FACE="Symbol">e</FONT> 31,000)nm [[Reference:Lewis_RA:Austen_KF:Drazen_JM:Clark_DA:Marfat_A:Corey_EJ:,Proc. Natl. Acad. Sci. U. S. A.,1980,77,3710|{{RelationTable/GetFirstAuthor|Reference:Lewis_RA:Austen_KF:Drazen_JM:Clark_DA:Marfat_A:Corey_EJ:,Proc. Natl. Acad. Sci. U. S. A.,1980,77,3710}}]]
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+{{Lipid/Footer}}