Al-Sanea, Mohammad M. Elkamhawy, Ahmed Zakaria, Ahmed Park, Byung Sun Kwon, Youngjoo Lee, So Ha Lee, Sang Woo Kim, In Tae 2024-01-20T08:02:44Z 2024-01-20T08:02:44Z 2021-09-05 2015-01 1420-3049 https://pubs.kist.re.kr/handle/201004/125935 A series of phenylbipyridinylpyrazoles was synthesized through the reaction of 2-(4-(2-chloropyridin-4-yl)-3-(3-methoxy-5-methylphenyl)-1H-pyrazol-1-yl) acetonitrile (4) with different 6-substituted pyridine-3-ylboronic acids. The final compounds 5a-j were screened at 10 mu M against over 60 tumor cell lines at the U.S. National Cancer Institute (NCI). In light of the NCI results, compounds 5c and 5h showed a broad spectrum of activity against NCI cell lines with mean growth of 53% and 58%, respectively. Compound 5e behaved differently as it showed high degree of selectivity and potency by inhibiting 96% of growth of leukemia SR cell line at 10 mu M. Standard COMPARE analyses were performed at the GI(50) level and the results exhibit high correlation in the form of pairwise correlation coefficient (PCC) of more than 0.6 between three of the current compounds and three standard known anticancer agents. Compound 5e demonstrated high correlation levels with merbarone (NSC S336628) with a PCC value of 0.631. Compound 5h showed a considerably high PCC value of 0.626 with dichloroallyl lawsone, while compound 5i, showed PCC values of 0.601 and 0.604 with both dichloroallyl lawsone and N,N-dibenzyldaunomycin (NSC S268242), respectively. These three standard agents have anticancer activity via two major mechanism of actions, inhibition of topoisomerase II and inhibition of biosynthesis of pyrimidine nucleotides, therefore, compounds 5a-j are promising therapeutic agents for targeting different human malignancies. Prediction of drug-likeness and toxicity of these newly synthesized derivatives were also considered. English MDPI TOPOISOMERASE-II-ALPHA DNA-TOPOISOMERASES INHIBITORS COMPARE DESIGN Synthesis and in Vitro Screening of Phenylbipyridinylpyrazole Derivatives as Potential Antiproliferative Agents Article 10.3390/molecules20011031 1 MOLECULES, v.20, no.1, pp.1031 - 1045 MOLECULES 20 1 1031 1045 scie scopus 000348319000061 2-s2.0-84921519604 Biochemistry & Molecular Biology Chemistry, Multidisciplinary Biochemistry & Molecular Biology Chemistry Article TOPOISOMERASE-II-ALPHA DNA-TOPOISOMERASES INHIBITORS COMPARE DESIGN cancer cell lines phenylbipyridinylpyrazole antiproliferative agents COMPARE analysis