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Synthesis In Vitro Antimicrobial and Cytotoxic Activities of Some New Pyrazolo15-apyrimidine Derivatives

机译:某些新型吡唑并15-a嘧啶衍生物的合成体外抗菌作用和细胞毒活性

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摘要

A new series of pyrazole >4–>7 and pyrazolo[1,5-a]pyrimidine >8–>13 were synthesized by using a simple, efficient procedure, and screened for their in-vitro antimicrobial and antitumor activities. Symmetrical and asymmetrical 3,6-diarylazo-2,5,7-triaminopyrazolo[1,5-a]pyrimidine were synthesized by the conventional method and also subjected to microwave irradiation and under ultrasound conditions. The biological results revealed that most of the tested compounds proved to be active as antibacterial and antifungal agents. The antitumor activity of the synthesized compounds was evaluated against human cancer cell lines, MCF-7, HCT-116, and HepG-2, as compared with Doxorubicin as a control.
机译:一系列新的吡唑> 4 – > 7 和吡唑并[1,5-a]嘧啶> 8 – > 13 通过简单,有效的方法合成,并对其体外抗菌和抗肿瘤活性进行了筛选。通过常规方法合成对称和不对称的3,6-二芳基偶氮-2,5,7-三氨基吡唑并[1,5-a]嘧啶,并在微波条件下和超声条件下进行合成。生物学结果表明,大多数被测化合物均具有抗菌和抗真菌活性。与作为对照的阿霉素相比,评估了合成化合物对人癌细胞系MCF-7,HCT-116和HepG-2的抗肿瘤活性。

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