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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >SYNTHESIS, CHARACTERIZATION AND EVALUATION OF ANTICANCER ACTIVITY OF SOME NEW SCHIFF BASES OF 1, 3, 4-THIADIAZOLE DERIVATIVES
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SYNTHESIS, CHARACTERIZATION AND EVALUATION OF ANTICANCER ACTIVITY OF SOME NEW SCHIFF BASES OF 1, 3, 4-THIADIAZOLE DERIVATIVES

机译:1,3,4-噻唑类衍生物的一些新希夫夫碱的合成,表征和抗癌活性评估

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摘要

Objective: N-benzylidene-5-phenyl-1, 3, 4-thiadiazol-2-amine derivatives: Synthesis and anticancer activity. Methods: In the present study five new derivatives of N-benzylidene-5-phenyl-1, 3, 4-thiadiazol-2-amine (Schiff bases containing 1, 3, 4-thiadiazole) were synthesized according to the literature methods and were characterized by FT-IR, 1 H NMR spectroscopy and C, H, N analysis. Anticancer activity was evaluated in Male Swiss albino mice using Ehrlich’s Ascites carcinoma cells. Compounds were administered at a dose of 25 mg/kg, body weight intraperitoneally. Results: The compounds were found to reduce tumor volume, viable cell count and increase the tumor weight (%) inhibition, ascites cells (%) inhibition, non-viable cell count and increase in life span (%ILS). All the compounds exhibited significant (P< 0.01) anticancer activity compared to control and the compound 2d & 4d was found to be most potent. Conclusion: It is concluded that synthesized Schiff bases of 2-amino-5-aryl-1, 3, 4-thiadiazoles derivatives are biologically active and developed into useful anticancer agents. Keywords: 1, 3, 4-Thiadiazole, Anticancer activity, Tumor cell count, Tumor weight inhibition.
机译:目的:N-亚苄基-5-苯基-1,3,4-噻二唑-2-胺衍生物:合成及抗癌活性。方法:在本研究中,根据文献方法合成了5种新的N-亚苄基-5-苯基-1,3,4-噻二唑-2-胺衍生物(席夫碱中含有1,3,4-噻二唑),并分别通过FT-IR,1 H NMR光谱和C,H,N分析进行表征。使用Ehrlich的腹水癌细胞对雄性瑞士白化病小鼠进行了抗癌活性评估。腹膜内以体重25mg / kg的剂量给予化合物。结果:发现这些化合物可减少肿瘤体积,活细胞计数并增加肿瘤重量(%)抑制,腹水细胞(%)抑制,非活细胞计数和寿命(%ILS)增加。与对照相比,所有化合物均显示出显着的(P <0.01)抗癌活性,并且发现化合物2d和4d最有效。结论:结论是合成的2-氨基-5-芳基-1、3、4-噻二唑衍生物的席夫碱具有生物活性,并已发展成为有用的抗癌剂。关键词:1、3、4-噻二唑,抗癌活性,肿瘤细胞计数,肿瘤重量抑制。

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