Author/Authors :
D.L. Gernert، نويسنده , , D.A. Neel، نويسنده , , M.F. Boehm، نويسنده , , M.D. Leibowitz، نويسنده , , D.A. Mais، نويسنده , , P.Y. Michellys، نويسنده , , D. Rungta، نويسنده , , A. Reifel-Miller، نويسنده , , T.A. Grese، نويسنده ,
Abstract :
Benzofused heterocyclic analogs of the RXR selective modulator 1 (LG101506) were synthesized, and tested for their ability to bind RXRα and activate RXR homo and heterodimers. Potency and efficacy were observed to be dependent upon the choice of heterocycle as well as the sidechain employed.
Keywords :
RXR , Heterocycles , Trienoic acid.* Corresponding authors. Tel.: +1-317-433-0430 , fax: +1-317-276-24-41 , e-mail addresses: dgernert@lilly.com , neelda@lilly.com
