306288-41-5Relevant academic research and scientific papers
Fluoro analogs of bioactive oxy-sterols: Synthesis of an EBI2 agonist with enhanced metabolic stability
Deng, Xiaohu,Sun, Siquan,Wu, Jiejun,Kuei, Chester,Joseph, Victory,Liu, Changlu,Mani, Neelakandha S.
supporting information, p. 4888 - 4891 (2016/10/05)
Synthesis of several 7-hydroxy oxysterols and their potential roles as signaling molecules in the innate and adaptive immune responses is discussed. Discovery of a new, fluorinated, synthetic analog of the 7α,25-dihydroxycholesterol—the endogenous ligand of GPR 183 (EBI2), a G-protein coupled receptor highly expressed upon Epstein–Barr virus infection is described. Fluoro oxysterol 12 showed good metabolic stability while maintaining excellent EBI2 agonist activity.
Synthesis of 7alpha-hydroxy derivatives of regulatory oxysterols.
Li,Spencer
, p. 529 - 535 (2007/10/03)
7alpha-Hydroxy derivatives of oxysterols are of considerable interest because of their possible involvement in regulation of cholesterol metabolism. This paper describes stereoselective syntheses and complete characterization of the 7alpha-hydroxy derivatives of four key oxysterols: 25-hydroxycholesterol, 27-hydroxycholesterol, 24(S)-hydroxycholesterol, and 24(S), 25-epoxycholesterol.
