Nasab Rezvan Rezaee, Hassanzadeh Farshid, Khodarahmi Ghadam Ali, Rostami Mahboubeh, Mirzaei Mahmoud, Jahanian-Najafabadi Ali, Mansourian Mahboubeh
Department of Medicinal Chemistry and Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Department of Pharmaceutical Biotechnology and Isfahan Pharmaceutical Sciences Research center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Res Pharm Sci. 2017 Oct;12(5):425-433. doi: 10.4103/1735-5362.213988.
A series of novel 4-anilinoquinazoline derivatives were designed and synthesized from benzoic acid through ring closure, chlorination or nucleophilic substitution. The structures of compounds were characterized by IR, H-NMR and mass spectroscopy. All synthesized derivatives were screened for their antimicrobial activities against Gram-positive (, , ) and Gram-negative (, , ) bacteria and also for antifungal activities against using the conventional micro dilution method. Most of the compounds have shown good antibacterial activities, especially compound having highest activities against at 32 μg/mL concentration while the tested compounds did not exhibited remarkable antifungal activities. The potential DNA gyrase inhibitory activity of these compounds was investigated using molecular docking simulation method. All compounds showed good results especially compound which showed the lowest ΔG results (-8.16 Kcal/mol).
通过环化、氯化或亲核取代反应,从苯甲酸出发设计并合成了一系列新型4-苯胺基喹唑啉衍生物。通过红外光谱(IR)、氢核磁共振谱(H-NMR)和质谱对化合物结构进行了表征。采用传统的微量稀释法,对所有合成衍生物针对革兰氏阳性菌( 、 、 )和革兰氏阴性菌( 、 、 )的抗菌活性以及针对 的抗真菌活性进行了筛选。大多数化合物表现出良好的抗菌活性,尤其是化合物 在32 μg/mL浓度下对 具有最高活性,而测试的化合物未表现出显著的抗真菌活性。利用分子对接模拟方法研究了这些化合物潜在的DNA促旋酶抑制活性。所有化合物均显示出良好结果,尤其是化合物 显示出最低的ΔG结果(-8.16千卡/摩尔)。