| Literature DB >> 15911262 |
Sheo B Singh1, John G Ondeyka, Weiguo Liu, Steve Chen, Tom S Chen, Xiaohua Li, Aileen Bouffard, James Dropinski, A Brian Jones, Sherrie McCormick, Nancy Hayes, Jianhua Wang, Neelam Sharma, Karen Macnaul, Melba Hernandez, Yu-Sheng Chao, Joanne Baffic, My-Hanh Lam, Charlotte Burton, Carl P Sparrow, John G Menke.
Abstract
Liver X receptors are nuclear receptors that regulate metabolism of cholesterol. They are activated by oxysterols resulting in increased transcription of the ABCA1 gene, promoting cholesterol efflux and HDL formation. We have identified podocarpic acid anhydride as a 1nM agonist of LXRalpha and beta receptors. Functionally this agonist was over 8-10-fold better activator of LXR receptors compared to one of the natural ligands, 22-(R)-hydroxy cholesterol, in HEK-293 cells. An imide analog increased the level of HDL by 26%, decreased LDL by 10.6%, and increased triglyceride by 51% in hamsters. Discovery, synthesis, SAR and details of the activities of dimers have been described.Entities:
Mesh:
Substances:
Year: 2005 PMID: 15911262 DOI: 10.1016/j.bmcl.2005.03.100
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823