发明名称 AnalogifremgangsmÕte for fremstilling av legemiddelavgivende porfyrinderivater
摘要 A compound is described having the structure <IMAGE> where R preferably is <IMAGE> and most preferably R3 is a closo-carborane and R2 is -H, an alkyl or aryl having 1 to about 7 carbon atoms, or a physiologically acceptable salt. Compounds of the invention are useful in boron neutron capture therapy, photodynamic therapy, and other biomedical applications. One embodiment we have designated 2,4-bis-[ alpha , beta -(1,2-dicarbaclosododecaborane carboxy)ethyl]deuteroporphyrin (x), appears not to pass through the normal blood brain barrier, has excellent water solubility, and has been shown efficacious in boron neutron capture therapy in vivo against the KHJJ mammary carcinoma.
申请公布号 NO303389(B1) 申请公布日期 1998.07.06
申请号 NO19930001843 申请日期 1993.05.19
申请人 REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE 发明人 KAHL, STEPHEN B.;KOO, MYOUNG-SEO
分类号 A61K31/69;A61K9/127;A61K41/00;A61K49/00;A61K51/00;A61K51/04;A61P35/00;C07F5/02;C07F5/05;(IPC1-7):C07F5/02;C07K15/16 主分类号 A61K31/69
代理机构 代理人
主权项
地址