2,4-Diphenyl-1,2-dihydroquinazoline Derivatives: Synthesis, Anticancer Activity and Docking Studies

被引:4
|
作者
Gudimella, Krishna Kanthi [1 ,2 ]
Bonige, Kishore Babu [1 ]
Gundla, Rambabu [2 ]
Katari, Naresh Kumar [2 ]
Yamajala, Bhaskar [2 ]
Battula, Venkateswara Rao [1 ]
机构
[1] Andhra Univ, Coll Engn, Dept Engn Chem, Visakhapatnam 530003, Andhra Pradesh, India
[2] GITAM Deemed Be Univ, Sch Sci, Dept Chem, Hyderabad 502329, India
来源
CHEMISTRYSELECT | 2019年 / 4卷 / 43期
关键词
Anticancer activity; Catalyst free; Dihydroquinazoline; Docking studies; ONE-POT SYNTHESIS; EFFICIENT SYNTHESIS; QUINAZOLINE; INHIBITORS; DESIGN; DISCOVERY; LIGAND;
D O I
10.1002/slct.201902609
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A straightforward, rapid and efficient one-pot method was developed for the synthesis of 2,4 -diphenyl-1,2 dihydroquinazoline and their analogues. The reactions were performed with different type of benzylamine and 2-bromo benzophenone using ammonium acetate and characterized by H-1 NMR, C-13 NMR and Mass spectroscopic techniques. All the compounds were tested for MDA-MB-231, A549 and DU-145 type of human cancer cell lines. Among the synthesized compounds, 4 j (4-phenyl-2-(3,4,5-trimethoxyphenyl)-1,2-dihydroquinazoline) and 4 e (2-(3,4-dichlorophenyl)-4-phenyl-1,2-dihydroquinazoline) molecules were found to possess good anticancer activity. The binding nature of these molecules was explored through docking studies.
引用
收藏
页码:12528 / 12533
页数:6
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