Design and discovery of novel thiazole derivatives as potential MMP inhibitors to protect against acute lung injury in sepsis rats via attenuation of inflammation and apoptotic oxidative stress
Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1,3-thiazole analogs
作者:Ghada S. Hassan、Shahenda M. El-Messery、Fatmah A.M. Al-Omary、Hussein I. El-Subbagh
DOI:10.1016/j.bmcl.2012.08.095
日期:2012.10
for their antitumoractivity, at a single dose of 10 μM. Most of the investigated compounds exhibited broad-spectrum antitumoractivity. Compounds 19 and 28 believed to be the most active members in this study, with MG-MID GI50, TGI, and LC50 values of 2.8, 11.4, 44.7; and 3.3, 13.1, 46.8, respectively. Compounds 19 and 28 proved to be nine and sevenfold more active than the standard antitumor drug 5-FU
设计并合成了一系列新的2-乙酰氨基-或2-丙酰胺基-4-(4-取代的苯基)-1,3-噻唑(11 – 34)。化合物以10μM的单剂量接受美国国家癌症研究所(NCI)的体外抗肿瘤活性评估。大多数研究的化合物表现出广谱抗肿瘤活性。化合物19和28被认为是该研究中最活跃的成员,其MG-MID GI 50,TGI和LC 50值为2.8、11.4、44.7。和3.3、13.1、46.8。事实证明,化合物19和28的活性分别比标准抗肿瘤药物5-FU高9倍和7倍。
Design and discovery of novel thiazole derivatives as potential MMP inhibitors to protect against acute lung injury in sepsis rats via attenuation of inflammation and apoptotic oxidative stress