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Eicosanoids chiral

Brash, A.R. and Hawkins, D.J. 1990. High-performance liquid chromatography for chiral analysis of eicosanoids. Methods Enzymol. 187 187-195. [Pg.417]

Chiral chromatography is widely used for the resolution of chiral isomers of eicosanoids and enantiomeric isomers of di- and monoacylglycerols. The technique and its applications were extensively reviewed by Prof. Ian Blair in relation to the targeted analysis of these lipid classes and individual species employing LC-MS [87-89]. [Pg.72]

Lee, S.H. and Blair, lA. (2009) Targeted chiral Upidomics analysis of bioactive eicosanoid lipids in cellular systems. BMB Rep. 42, 401 10. [Pg.85]

At the beginning of this chapter, we have noted that the stereochemical composition of an eicosanoid may be indicative of the enzymatic system through which the compound is produced. Therefore, positive conclusions as to the enzymatic origin of a given eicosanoid can be best drawn when the product s stereochemistry is precisely defined. This task can be accomplished now with relative ease by HPLC on chiral-phase columns. This method and other methods used in the chiral analysis of arachidonate metabolites have been reviewed. ... [Pg.84]

See other pages where Eicosanoids chiral is mentioned: [Pg.152]    [Pg.536]    [Pg.541]    [Pg.541]    [Pg.647]    [Pg.665]    [Pg.669]    [Pg.11]    [Pg.187]    [Pg.108]    [Pg.332]    [Pg.1119]    [Pg.1119]    [Pg.141]   
See also in sourсe #XX -- [ Pg.72 ]



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Eicosanoids

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