作者:Kee-In Lee、Youmie Park、Su-Jin Park、Jung-Hwan Hwang、Sung-Jin Lee、Gun-Do Kim、Woo-Kyu Park、Sunghou Lee、Daeyoung Jeong、Jae-Yang Kong、Hee-Kyoung Kang、Heeyeong Cho
DOI:10.1016/j.bmcl.2005.08.115
日期:2006.2
dinaphtho[1,2-b;2',3'-d]furan-7,12-dione derivatives were synthesized and evaluated for inhibitory activities against receptor tyrosine kinases. The naphthofuroquinone compounds with dialkylaminoethoxy group at C(5)-position (7, 8, 10, and 11) manifested strong inhibitory activities against epidermal growth factor receptor and vascular endothelial growth factor receptor. Docking study of 11 with EGFR was
合成了一系列二萘并[1,2-b; 2',3'-d]呋喃-7,12-二酮衍生物,并评估了其对受体酪氨酸激酶的抑制活性。在C(5)-位置(7、8、10和11)具有二烷基氨基乙氧基的萘并呋喃醌化合物表现出对表皮生长因子受体和血管内皮生长因子受体的强抑制活性。还进行了11与EGFR的对接研究。