Synthesis, Characterization, and Biological Evaluation of Tetrahydropyrimidines: Dual-Activity and Mechanism of Action
作者:Emilija Milović、Nenad Janković、Jelena Petronijević、Nenad Joksimović、Marijana Kosanić、Tatjana Stanojković、Ivana Matić、Nađa Grozdanić、Olivera Klisurić、Srđan Stefanović
DOI:10.3390/pharmaceutics14102254
日期:——
In this paper, the synthesis, characterization, and biological evaluation of the novel tetrahydropyrimidines—THPMs are described. THPMs are well-known for wide pharmacological activities such as antimicrobial, anticancer, antiviral, etc. This research includes obtained results of in vitro antimicrobial, anticancer, and α-glucosidase inhibitory activities of the eleven novel THPMs. An antibiotic assessment
本文介绍了新型四氢嘧啶—THPMs的合成、表征和生物学评价。THPMs 因其广泛的药理活性而闻名,如抗菌、抗癌、抗病毒等。本研究包括获得的 11 种新型 THPMs 的体外抗菌、抗癌和 α-葡萄糖苷酶抑制活性的结果。通过使用肉汤管稀释法确定最小抑制浓度 (MIC),对五种细菌(两种革兰氏阳性和三种革兰氏阴性)和五种真菌进行了抗生素评估。抗菌活性最强的化合物是4a、4b和4d,而抗菌活性最好的是4e、4f和4d 。4k。测量了4e、4f和4k对须癣毛癣菌的最低 MIC 值 (0.20 mg/mL) 。此外,检查α-葡萄糖苷酶抑制活性表明化合物4g是具有最佳活性的化合物。对肿瘤细胞系(HeLa、K562 和 MDA-MB-231)和正常细胞(MRC-5)进行细胞毒活性。化合物4b和4k对 HeLa 细胞系显示出最好的抗肿瘤活性。还研究了最活跃的化合物对细胞周期的影响和作用机制。化合物4b具有良