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Synthesis and biological evaluation of novel fused triazolo[4,3-a] pyrimidinones

Chia sẻ: Lăng Thần Nam | Ngày: | Loại File: PDF | Số trang:22

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The antimicrobial activity of the products was evaluated and the results revealed that compounds 8f and 15f showed strong activity against gram-positive bacteria while compound 15d showed the highest activity against gramnegative bacteria. Moreover, compounds 15b, 8d, 8e, 8c, 8l, and 8j exhibited significant antifungal activity. In addition, the antitumoral activity of the synthesized products against different cancer cell lines was determined and the results revealed that compound 12c was the most active against MCF-7, HepG-2, HCT-116, and HeLa with IC50 values of 0.51, 0.72, 0.95, and 0.95, respectively, as compared with doxorubicin as positive control.

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Nội dung Text: Synthesis and biological evaluation of novel fused triazolo[4,3-a] pyrimidinones

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