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ID: ALA1140778

Journal: Bioorg Med Chem Lett

Title: Carboxylic acid based quinolines as liver X receptor modulators that have LXRbeta receptor binding selectivity.

Authors: Hu B, Quinet E, Unwalla R, Collini M, Jetter J, Dooley R, Andraka D, Nogle L, Savio D, Halpern A, Goos-Nilsson A, Wilhelmsson A, Nambi P, Wrobel J.

Abstract: A series of potent and binding selective LXRbeta agonists was developed using the previously reported non-selective LXR ligand WAY-254011 as a structural template. With the aid of molecular modeling, it was found that 2,3-diMe-Ph, 2,5-diMe-Ph, and naphthalene substituted quinoline acetic acids (such as quinoline 33, 37, and 38) showed selectivity for LXRbeta over LXRalpha in binding assays.

CiteXplore: 18023179

DOI: 10.1016/j.bmcl.2007.11.013