encequidar 、 盐酸 以to obtain 1.4 g of the title compound (yield 89%)的产率得到4-oxo-4H-chromene-2-carboxylic acid [2-(2-{4-[2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-phenyl}-2H-tetrazol-5-yl)-4,5-dimethoxy-phenyl]-amide hydrochloride
参考文献:
名称:
P-glycoprotein inhibitor, method for preparing the same and pharmaceutical composition comprising the same
P-glycoprotein inhibitor, method for preparing the same and pharmaceutical composition comprising the same
申请人:Bang Chan Keuk
公开号:US20070072900A1
公开(公告)日:2007-03-29
The bioavailability of an anticancer agent is enhanced when the anticancer agent is administered together with a pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof.