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PPAR cofactors

Halofenic acid is a SPPARM that functions primarily as a partial agonist characterized by the differential recruitment of PPAR cofactors, i.e. displacement of corepressors [NCoR and silencing mediator for retinoid and thyroid receptors (SMRT)] and inefficient recruitment of coactivators [cAMP response element binding protein (CREB) binding protein (CBP) and TRAP220] [73]. When dosed orally to diabetic mice and rats as the acetamidoethyl ester, halofenic acid produces insulin sensitization comparable to rosiglitazone without increases in body weight. [Pg.380]


See other pages where PPAR cofactors is mentioned: [Pg.371]    [Pg.371]    [Pg.371]    [Pg.371]    [Pg.78]    [Pg.203]    [Pg.635]    [Pg.58]    [Pg.372]    [Pg.147]    [Pg.915]    [Pg.333]    [Pg.165]    [Pg.233]    [Pg.3817]   
See also in sourсe #XX -- [ Pg.371 ]




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