Design, synthesis and biological evaluation of novel molecules as potent PARP-1 inhibitors.

ID: ALA4819147

Journal: Bioorg Med Chem Lett

Title: Design, synthesis and biological evaluation of novel molecules as potent PARP-1 inhibitors.

Authors: Shen H, Ge Y, Wang J, Li H, Xu Y, Zhu Q.

Abstract: Two series of novel compounds with inhibition activity against PARP-1 were designed and synthesized. All target compounds were evaluated for their PARP-1 inhibition activity, and compounds with high PARP-1 inhibition activity were selected to assess for cellular assays in vitro. Among them, compound II-4 displayed impressive results in both PARP-1 enzyme inhibition with IC₅₀ value of 0.51 nM and anti-proliferation activity against HCT116 and HCC1937 cell lines with IC₅₀ values of 6.62 nM and 12.65 nM, respectively. Also, II-4 exhibited good metabolic stability in vitro with t_1/2 of 173.25 min and CL_int of 0.04 mL/min/mg. Prediction of molecular properties and protein docking were applied to structure design. Our study provides potential lead compounds and design directions for the development of PARP-1 inhibitors.

CiteXplore: 34091044

DOI: 10.1016/j.bmcl.2021.128169

Patent ID: ┄