Design, synthesis, and cytotoxic evaluation of quinazoline derivatives bearing triazole-acetamides. Issue 2 (February 2023)

• Record Type: Journal Article
• Authors: Pedrood, Keyvan; Taayoshi, Fahimeh; Moazzam, Ali; Iraji, Aida; Yavari, Ali; Ansari, Samira; Sajjadi-Jazi, Sayed Mahmoud; Mohajeri-Tehrani, Mohammad Reza; Garmsiri, Nadia; Haghpanah, Vahid; Soleymanibadi, Meysam; Larijani, Bagher; Hamedifar, Haleh; Adibpour, Neda; Mahdavi, Mohammad
• Is Part Of: Heliyon. Volume 9:Issue 2(2023)
• Publication Date: 2023-02
• Subjects: Anticancer activity -- Click chemistry -- Docking -- Quinazoline; Research -- Periodicals; Medical sciences -- Periodicals; Natural history -- Periodicals; Social sciences -- Periodicals; Earth sciences -- Periodicals; Physical sciences -- Periodicals; 507.2
• DOI: 10.1016/j.heliyon.2023.e13528
• Languages: English
• ISSNs: 2405-8440

Abstract

Abstract: A novel series of quinazoline-based agents bearing triazole-acetamides 8a-l were designed and synthesized. All the obtained compounds were tested for in vitro cytotoxic activities against three human cancer cell lines named HCT-116, MCF-7, and HepG2, as well as a normal cell line WRL-68 after 48 and 72 h. The results implied that quinazoline-oxymethyltriazole compounds exhibited moderate to good anticancer potential. The most potent derivative against HCT-116 was 8a (X = 4-OCH3 and R = H) with IC50 values of 10.72 and 5.33 μM after 48 and 72 h compared with doxorubicin with IC50 values of 1.66 and 1.21 μM, respectively. The same trend was seen in the HepG2 cancerous cell line in which 8a recorded the best results with IC50 values of 17.48 and 7.94 after 48 and 72 h, respectively. The cytotoxic analysis against MCF-7 showed that 8f with IC50 = 21.29 μM (48 h) exhibited the best activity, while compounds 8k (IC50 = 11.32 μM) and 8a (IC50 = 12.96 μM), known as the most effective cytotoxic agents after 72 h. Doxorubicin as positive control exhibited IC50 values of 1.15 and 0.82 μM after 48 and 72 h, respectively. Noteworthy, all derivatives showed limited toxicity against the normal cell line. Moreover, docking studies were also presented to understand the interactions between these novel derivatives and possible targets.