
is a synthetic selective, active non-steroidal liver X receptor (LXR) agonist μM for hLXRα and hLXRβ, respectively. Angiotensin II-mediated increases reduced by GW3965 HCl . In HepG2 cells, the EC50 for GW3965 is greater GW3965 HCl decreased lesion area by 53% 34% in male and female induced expression of ATP-binding cassettes A1 and G1 in modified macrophages in vitro as well as in the aortas of hyperlipidemic mice.