查尔酮
化学
抗菌活性
体内
吡唑啉
金黄色葡萄球菌
立体化学
淋病奈瑟菌
细胞毒性
药理学
体外
微生物学
生物化学
细菌
生物
药物化学
遗传学
生物技术
作者
Jonathan Ramírez–Prada,Juan S. Rocha‐Ortiz,Marta I. Orozco,Pedro A. Moreno,Miguel Guevara,Mauricio Barreto,María Elena Burbano,Sara M. Robledo,María del Pilar Crespo-Ortiz,Jairo Quiroga,Rodrigo Abonı́a,Viviana Cuartas,Braulio Insuasty
标识
DOI:10.1002/ardp.202400081
摘要
New pyridine-based chalcones 4a-h and pyrazolines 5a-h (N-acetyl), 6a-h (N-phenyl), and 7a-h (N-4-chlorophenyl) were synthesized and evaluated by the National Cancer Institute (NCI) against 60 different human cancer cell lines. Pyrazolines 6a, 6c-h, and 7a-h satisfied the pre-determined threshold inhibition criteria, obtaining that compounds 6c and 6f exhibited high antiproliferative activity, reaching submicromolar GI
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