Bisbenzoxazole derivatives had anti-proliferative effect on Human Cancer Cells

Furkan Ayaz, Qadar Ahmed Isse, Rusmeenee Kheeree, R. Ersan, Oztekin Algul
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引用次数: 4

Abstract

A series of symmetric bis-benzoxazole derivatives were synthesized using one-pot cyclisation reaction between 4-fluoro substituted 2-aminophenol and suitable carboxylic acids. Synthesized compounds’ anticancer activities were tested by using MTT assay on human prostate (DU145) and breast (MCF7) cancer cells. Screening results revealed that all compounds possessed a high level anti-cancer potential by significantly decreasing the cell proliferation in prostate and breast cancer cell lines. Our compounds exerted their anti-proliferative effects in a dose and time dependent manner. Our results suggest that they can be highly potent since they were biologically active even at low concentration ranges. Our study presents a series of new bis-benzoxazole based compounds with potential therapeutic effects against tumor cells. Therefore, characterization of new generation bis-benzoxazole derivatives will have a significant contribution on the development of new era anti-cancer drug candidates.
双苯并恶唑衍生物对人癌细胞具有抗增殖作用
以4-氟取代的2-氨基苯酚和合适的羧酸为原料,采用一锅环化反应合成了一系列对称的双苯并恶唑衍生物。用MTT法检测合成的化合物对人前列腺(DU145)和乳腺癌(MCF7)癌细胞的抗癌活性。筛选结果显示,所有化合物均具有高水平的抗癌潜力,可显著降低前列腺癌和乳腺癌细胞系的细胞增殖。化合物的抗增殖作用呈剂量和时间依赖性。我们的研究结果表明,即使在低浓度范围内,它们也具有很强的生物活性。我们的研究提出了一系列新的基于双苯并恶唑的化合物,对肿瘤细胞具有潜在的治疗作用。因此,新一代双苯并恶唑衍生物的表征将对新时代抗癌候选药物的开发有重大贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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