Drug Design and Medicinal Chemistry Lab, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.
Department of Pharmacology, College of Pharmacy, Jazan University, PO Box 114, Gizan, Saudi Arabia.
Bioorg Chem. 2019 Jun;87:667-678. doi: 10.1016/j.bioorg.2019.03.071. Epub 2019 Mar 29.
Meagre and suboptimal therapeutic response along with the side effect profile associated with the existing anticancer therapy have necessitated the development of new therapeutic modalities to curb this disease. Bearing in mind the current scenario, a series of 1,2,3-triazole linked 3-(1,3-diphenyl-1H-pyrazol-4-yl)acrylates was synthesized following a multi-step reaction scheme. Initial screening for anticancer potential was done by in vitro sulforhodamine B assay against four human cancer cell lines- MCF-7 (breast), A549 (Lung) and HCT-116 and HT-29 (Colon). On evaluation, several compounds showed promising growth inhibition against all the cell lines, particularly compounds 6e, 6f and 6n. Among them, compound 6f displayed IC values of 1.962, 3.597, 1.764 and 4.496 µM against A549, HCT-116, MCF-7 and HT-29 cell lines respectively. Furthermore, the apoptosis inducing potential of the compounds was determined by Hoechst staining and DNA fragmentation assay. Colony formation inhibition assay was also carried out to determine the long term cytotoxic potential of the molecules. Moreover, compounds 6e, 6f and 6n were also evaluated for anti-inflammatory activity by protein albumin denaturation assay and red blood cell membrane stabilizing assay.
由于现有的抗癌疗法疗效不佳且存在副作用,因此需要开发新的治疗方法来抑制这种疾病。考虑到当前的情况,我们按照多步反应方案合成了一系列连接 1,2,3-三唑的 3-(1,3-二苯基-1H-吡唑-4-基)丙烯酰胺。通过体外磺酰罗丹明 B 测定法对四种人癌细胞系-MCF-7(乳腺)、A549(肺)和 HCT-116 和 HT-29(结肠)进行了初步的抗癌潜力筛选。评估结果表明,几种化合物对所有细胞系均显示出有希望的生长抑制作用,特别是化合物 6e、6f 和 6n。其中,化合物 6f 对 A549、HCT-116、MCF-7 和 HT-29 细胞系的 IC 值分别为 1.962、3.597、1.764 和 4.496µM。此外,通过 Hoechst 染色和 DNA 片段化测定法确定了化合物的诱导凋亡潜力。还进行了集落形成抑制测定法以确定分子的长期细胞毒性潜力。此外,还通过蛋白白蛋白变性测定法和红细胞膜稳定测定法评估了化合物 6e、6f 和 6n 的抗炎活性。