Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2
作者:Myung-Ho Jung、Mohammed I. El-Gamal、Mohammed S. Abdel-Maksoud、Taebo Sim、Kyung Ho Yoo、Chang-Hyun Oh
DOI:10.1016/j.bmcl.2012.05.004
日期:2012.7
A new series of diarylureas and diarylamides possessing 1H-pyrrolo[3,2-c]pyridine scaffold was designed and synthesized. Their in vitro antiproliferative activities against A375P human melanoma cell line and NCI-9 human melanoma cell line panel were tested. All the target compounds, except three amino derivatives 8g, h and 9h, demonstrated superior potencies against A375P to Sorafenib. In addition
设计并合成了一系列新的具有1 H-吡咯并[3,2- c ]吡啶骨架的二芳基脲和二芳基酰胺。测试了它们对A375P人黑素瘤细胞系和NCI-9人黑素瘤细胞系的体外抗增殖活性。除了三种氨基衍生物8g,h和9h以外,所有目标化合物均显示出对A375P优于索拉非尼的效力。此外,化合物8a和9b – f的抗药性比维拉非尼高,抗A375P的能力更强。化合物8c和9b分别比NIH3T3成纤维细胞对A375P黑色素瘤细胞的选择性高7.50倍和454.90倍。此外,化合物8d,e和9a – d,f在NCI上表现出对九种经过测试的黑色素瘤细胞系的极高效能。双酰胺衍生物9a – c,f在NCI-9黑色素瘤细胞系的不同细胞系上显示2位的纳摩尔IC 50值。