Farag, Ahmed Karam Hassan, Ahmed H. E. Chung, Kyung-Sook Lee, Jeong-Hun Gil, Hyo-Sun Lee, Kyung-Tae Roh, Eun Joo 2024-01-19T16:31:50Z 2024-01-19T16:31:50Z 2022-01-25 2020-10 0045-2068 https://pubs.kist.re.kr/handle/201004/118022 A series of diarylurea derivatives comprising 2,4-diarylpyrimidines were synthesized based on a combination of postulated molecular hybridization design and failed-ligands repurposing approaches, which enabled the discovery of novel potential antiproliferative agents. Towards credible biological evaluation, an in vitro anticancer activity assay was conducted employing a library of 60 cancer cell lines constituting nine panels representing blood, lung, colon, CNS, skin, ovary, renal, prostate, and breast cancers. The results revealed high effectiveness and broad-spectrum anticancer activity of compounds 4m and 4g. Five-dose assay of compounds 4m and 4g proved their high potency that surpassed that of four standard kinase inhibitors FDA-approved anticancer drugs against many cancer cells. Towards the identification of their molecular target, screening of kinase inhibitory profile employing a panel of 51 kinases involved in cancer revealed inhibition of several kinases from the platelet-derived growth factor/vascular endothelial growth factor receptor (PVR) kinase family, which might mediate, at least in part, the antiproliferative activity. Molecular docking of 4g into the crystal structure of the Feline McDonough Sarcoma (FMS) kinase predicted that it binds to a pocket formed by the juxtamembrane domain, the catalytic loop, and the aE helix, thus stabilizing the inhibited conformation of the kinase. Flow cytometric study of the cytotoxic effects of compound 4g in A549 cells showed it induces dose- and timedependent apoptotic events leading to cell death. Collectively, this work presents compound 4g as a potential broad-spectrum anticancer agent against multiple cancer types. English ACADEMIC PRESS INC ELSEVIER SCIENCE Diarylurea derivatives comprising 2,4-diarylpyrimidines: Discovery of novel potential anticancer agents via combined failed-ligands repurposing and molecular hybridization approaches Article 10.1016/j.bioorg.2020.104121 1 BIOORGANIC CHEMISTRY, v.103 BIOORGANIC CHEMISTRY 103 N scie scopus 000575792000005 2-s2.0-85088996917 Biochemistry & Molecular Biology Chemistry, Organic Biochemistry & Molecular Biology Chemistry Article TUMOR HETEROGENEITY DUAL INHIBITORS ANALOGS DESIGN CANCER HYBRIDS ASSAY CYTOTOXICITY RESISTANCE MUTATIONS DOCKING Diarylurea derivatives 2,4-Diarylpyrimidnes Repurposing Molecular hybridization Anticancer