SYNTHESIS AND ANTILEUKEMIC ACTIVITY OF ETOPOSIDE A-RING ANALOGS

被引:8
作者
KADOW, JF
TUN, MM
CROSSWELL, AR
ROSE, WC
VYAS, DM
DOYLE, TW
机构
[1] Bristol-Myers Squibb Company, Wallingford, CT 06492
关键词
D O I
10.1016/S0960-894X(00)80646-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The A ring of the clinical antitumor agent, etoposide, was opened to a protected 6,7-diphenol which was derivatized to form a number of new analogs. These compounds displayed activity inferior to etoposide when evaluated against several tumor cell lines in vitro and against murine P388 leukemia in vivo.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 23 条
[11]  
LONG BH, 1991, CANCER RES, V51, P5275
[12]  
LONG BH, 1983, P AM ASSOC CANC RES, V24, P321
[13]  
LONG BH, 1984, J BIOL CHEM, V259, P13560
[14]   INHIBITION OF THE DNA CATENATION ACTIVITY OF TYPE-II TOPOISOMERASE BY VP16-213 AND VM26 [J].
MINOCHA, A ;
LONG, BH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 122 (01) :165-170
[15]  
ROSE WC, 1986, ANTICANCER RES, V6, P557
[16]  
ROSE WC, 1983, CANCER RES, V43, P1504
[17]  
ROSS W, 1984, CANCER RES, V44, P5857
[18]   E-RING DEOXY ANALOGS OF ETOPOSIDE [J].
SAULNIER, MG ;
VYAS, DM ;
LANGLEY, DR ;
DOYLE, TW ;
ROSE, WC ;
CROSSWELL, AR ;
LONG, BH .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (07) :1418-1420