Bülbül, BahadırDing, KaiZhan, Chang-GuoÇftçi, GamzeYelekci, KemalGürboğa, MerveÖzakpınar, Özlem Bingöl2023-07-262023-07-2620221381-19911573-501Xhttps://doi.org/10.1007/s11030-022-10551-0https://hdl.handle.net/20.500.12684/12449Some novel triazole-bearing ketone and oxime derivatives were synthesized from Ibuprofen. In vitro cytotoxic activities of all synthesized molecules against five cancer lines (human breast cancer MCF-7, human lung cancer A549, human prostate cancer PC-3, human cervix cancer HeLa, and human chronic myelogenous leukemia K562 cell lines) were evaluated by MTT assay. In addition, mouse embryonic fibroblast cells (NIH/3T3) were also evaluated to determine the selectivity. Compounds 18, 36, and 45 were found to be the most cytotoxic, and their IC50 values were in the range of 17.46-68.76 mu M, against the tested cancer cells. According to the results, compounds 7 and 13 demonstrated good anti-inflammatory activity against the microsomal enzyme prostaglandin E2 synthase-1 (mPGES-1) enzyme at IC50 values of 13.6 and 4.95 mu M. The low cytotoxicity and non-mutagenity of these compounds were found interesting. Also, these compounds significantly prevented tube formation in angiogenesis studies. In conclusion, the anti-inflammatory and angiogenesis inhibitory activities of these compounds without toxicity suggested that they may be promising agents in anti-inflammatory treatment and they may be supportive agents for the cancer treatment. [GRAPHICS] .en10.1007/s11030-022-10551-0info:eu-repo/semantics/closedAccess1,2,4-Triazole; Atropisomer; Diastereotope; X-Ray Diffraction; Cancer; Angiogenesis; Mpges-1; CytotoxicityProstaglandin-E Synthase-1; Antiinflammatory Activity; Hybrids Synthesis; Beta-Catenin; Tumor-Growth; Derivatives; Cox-2; Discovery; Design; AntibacterialArticle363317862-s2.0-85141412569WOS:000878961700002Q2Q2