Synthesis and Antiproliferative Activity of Some Androstene Oximes and Their O-Alkylated Derivatives

被引:16
作者
Acharya, Pratap Chandra [1 ]
Bansal, Ranju [1 ]
机构
[1] Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India
关键词
Antileukemic activity; Cytotoxic steroids; Oxime ethers; Steroidal oximes; ANTINEOPLASTIC ACTIVITY; CANCER-THERAPY; BREAST-CANCER; STEROIDS;
D O I
10.1002/ardp.201300216
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In order to study the structure-activity relationship with respect to the cytotoxicity of steroidal oximes, several 6E-hydroximino-4-ene steroids and their O-alkylated derivatives were synthesized. The oxime ethers were solidified and purified by preparing their corresponding oxalate salts. The new derivatives as well as some previously synthesized ones were evaluated for in vitro antineoplastic activity against a panel of 60 cancer cell lines at 10 mu M. The oximes and oxime ethers were found to have moderate to good antiproliferative activity against various leukemia, colon, melanoma, and renal cancer cell lines.
引用
收藏
页码:193 / 199
页数:7
相关论文
共 20 条
[1]   MODIFIED STEROID HORMONES .5. 6-METHYLANDROSTANE DERIVATIVES [J].
ACKROYD, M ;
ADAMS, WJ ;
ELLIS, B ;
PETROW, V ;
STUARTWEBB, IA .
JOURNAL OF THE CHEMICAL SOCIETY, 1957, (SEP) :4099-4105
[2]   Synthesis and Antineoplastic Activity of O-Alkylated Derivatives of 7-Hydroximinoandrost-5-ene Steroids [J].
Bansal, Ranju ;
Guleria, Sheetal ;
Ries, Christina ;
Hartmann, Rolf W. .
ARCHIV DER PHARMAZIE, 2010, 343 (07) :377-383
[3]  
Blagosklonny MV, 2004, CELL CYCLE, V3, P1035
[4]  
Carlos J., 1997, TETRAHEDRON LETT, V38, P1833
[5]   GLUCOCORTICOIDS IN CANCER-THERAPY [J].
COLEMAN, RE .
BIOTHERAPY, 1992, 4 (01) :37-44
[6]  
COOMBES RC, 1992, EUR J CANCER, V28A, P1941
[7]  
DEGTEVA S. A., 1964, VOP ONKOL, V10, P52
[8]   Synthesis of cytotoxic 6E-hydroximino-4-ene steroids:: Structure/activity studies [J].
Deive, N ;
Rodríguez, J ;
Jiménez, C .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (16) :2612-2618
[9]  
Golubovskaia L E, 2006, Bioorg Khim, V32, P221
[10]   Synthesis and evaluation of novel steroidal oxime inhibitors of P450 17 (17α-hydroxylase/C17-20-lyase) and 5α-reductase types 1 and 2 [J].
Hartmann, RW ;
Hector, M ;
Haidar, S ;
Ehmer, PB ;
Reichert, W ;
Jose, J .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (22) :4266-4277