化学
癌症研究
癌症
激酶
吡啶
癌细胞
细胞培养
抑制性突触后电位
癌
立体化学
生物化学
药理学
内科学
药物化学
生物
医学
遗传学
作者
Wagdy M. Eldehna,Maha-Hamadien Abdulla,Mohamed S. Nafie,Ahmed E. Elsawi,Salsabil Ayman,Mai I. Shahin,Noura Alhassan,Ahmad Zubaidi,Hazem A. Ghabbour,Mahmoud M. Elaasser,Ahmed A. Al‐Karmalawy,Hatem A. Abdel‐Aziz
标识
DOI:10.1016/j.bioorg.2024.107778
摘要
In the current medical era, human health is confronted with various challenges, with cancer being a prominent concern. Therefore, enhancing the therapeutic arsenal for cancer with a constant influx of novel molecules that selectively target tumor cells while displaying minimal toxicity toward normal cells is imperative. This study delves into the antiproliferative and EGFR kinase inhibitory activities of newly reported spirooxindole-pyrazolo[3,4-b]pyridine derivatives 8a-h and 10a-h. The inhibitory effects on the growth of human cancer cell lines A-549 (lung carcinoma), Panc-1 (pancreatic carcinoma), and A-431 (skin epidermoid carcinoma) were evaluated, and the SAR has been clarified through analysis. With IC
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