Synthesis and Characterization of Novel N-Benzylbenzimidazole Linked Pyrimidine Derivatives as Anticancer Agents

被引:11
作者
Padhy, Gopal Krishna [1 ,2 ]
Panda, Jagadeesh [3 ]
Behera, Ajaya Kumar [1 ]
机构
[1] Sambalpur Univ, Sch Chem, Organ Synth Lab, Burla 768019, Odisha, India
[2] Maharajahs Coll Pharm, Dept Pharmaceut Chem, Vizianagaram, Andhra Pradesh, India
[3] Raghu Coll Pharm, Dept Pharmaceut Chem, Visakhapatnam, Andhra Pradesh, India
关键词
Chalcone; Benzimidazole; Pyrimidine; Anticancer activity; SRB assay; DISCOVERY; KINASE; BENZIMIDAZOLES; INHIBITORS; GROWTH; DESIGN; POTENT;
D O I
10.5530/ijper.53.2s.57
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Background: Emergence of resistance to accessible anticancer drugs became a threat to human lives in the recent time. To address this issue, discovery of novel anticancer agents becomes very essential. Benzimidazoles and pyrimidines have been reported to possess potent anticancer activity. Materials and Methods: A hybrid approach has been used, in which core structure of potentially active N-benzyl benzimidazole and pyrimidine derivatives are brought together in to a single molecule. The desired compounds were prepared by the condensation of N-benzyl benzimidazole chalcones with guanidine hydrochloride. The synthesized compounds were characterized using spectral studies (IR, H-1, C-13-NMR techniques and mass spectrometry). All the compounds were screened for their anticancer activity against human breast cancer cell line MDA-MB-231. Results: The spectral data's are in well agreement with the synthesized compounds 5a-e. Compounds 5b (GI(50) = 39.6 mu M) and 5a (GI(5)(0) = 84.0 mu M) exhibited significant anticancer activity. Conclusion: Owing to the anticancer activity, compound 5b can be used as lead structure in the development of yet more potent anticancer agents.
引用
收藏
页码:S129 / S134
页数:6
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