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Campesterol formation

Microwave-assisted catalytic hydrogenation of steroid compounds, e. g. cholesterol, campesterol, sitosterol, etc., in the presence of Pd/C catalyst and ammonium formate in glycol solvent was fast and afforded the corresponding products in high yield (80-95%) and purity [42]. [Pg.353]

Unsaturated sterols such as cholesterol, campesterol, sitosterol and bile alcohols with unsaturated side chains can be transfer hydrogenated efficiently and with high yields under microwave irradiation, using ammonium formate and a Pd/C catalyst in methylene chloride/propylene glycol solvents (Scheme 4.3)17. [Pg.77]

The enzyme studied by Garcia and Mudd (1978d) did not distinguish between [ C]cholesterol and [ C]sitosterol in the formation of SE. Competition studies on sterols for [ C]cholesterol further indicated no specificity in the use of campesterol. The Km for cholesterol and sitosterol was estimated to be 57 pM. [Pg.524]

In D. tertiolecta, we were able to idenhfy the majority of enzymes responsible for the biosynthesis of stigmasterol and p-sitosterol. We have also identified the enzymes synthesizing episterol, a precursor of campesterol, which is an important phytosterol known to have potential antiosteoarthritic properties (Gabay et al., 2010). Episterol is also a precursor for ergosterol however, the biosynthetic pathway branches after (S)-squalene-2,3-epoxide formation and follows a different route. Due to the fact that we did not identify most of the... [Pg.344]


See other pages where Campesterol formation is mentioned: [Pg.247]    [Pg.417]    [Pg.417]    [Pg.181]    [Pg.529]    [Pg.57]    [Pg.347]   
See also in sourсe #XX -- [ Pg.419 ]




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