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Synthesis and biological evaluation of some novel fused pyrazolopyrimidines as potential anticancer and antimicrobial agents.

机译:一些新型融合的吡唑并嘧啶类化合物作为潜在的抗癌和抗菌药物的合成和生物学评估。

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摘要

Synthesis and evaluation of anticancer and antimicrobial activity of some novel pyrazolopyrimidines and fused pyrazolopyrimidines are reported. Twelve analogs were selected to be evaluated for their in vitro anticancer potential against a panel of three human tumor cell lines: hepatocellular carcinoma HepG2, cervical carcinoma HelaS3 and colon carcinoma CaCo. The obtained data revealed that eight compounds namely; 6b, 6d, 7c, 8c, 10b, 12b, 13a and 13b were able to exhibit variable degrees of anticancer activities against the three used cell lines, of which compound 6d proved to be the most active. On the other hand, all the newly synthesized compounds were subjected to in vitro antibacterial and antifungal screening. Almost all the tested compounds were found to possess variable degrees of antimicrobial activities. Collectively, compounds 7c, 8c, 12b, 13a and 13b could be considered as possible agents with dual anticancer and antimicrobial activities.
机译:报道了一些新颖的吡唑并嘧啶和稠合的吡唑并嘧啶的合成及抗癌和抗菌活性评估。选择十二种类似物以评估其对三种人类肿瘤细胞系的体外抗癌潜力:肝细胞癌HepG2,宫颈癌HelaS3和结肠癌CaCo。得到的数据表明,有八个化合物。 6b,6d,7c,8c,10b,12b,13a和13b能够对三种使用过的细胞系表现出不同程度的抗癌活性,其中化合物6d被证明是活性最高的。另一方面,所有新合成的化合物均经过体外抗菌和抗真菌筛选。发现几乎所有测试的化合物都具有不同程度的抗菌活性。化合物7c,8c,12b,13a和13b共同被认为是具有双重抗癌和抗菌活性的可能药物。

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