DNA-DIRECTED ALKYLATING-AGENTS .5. ACRIDINECARBOXAMIDE DERIVATIVES OF (1,2-DIAMINOETHANE)DICHLOROPLATINUM(II)

被引:69
作者
LEE, HH
PALMER, BD
BAGULEY, BC
CHIN, M
MCFADYEN, WD
WICKHAM, G
THORSBOURNEPALMER, D
WAKELIN, LPG
DENNY, WA
机构
[1] UNIV AUCKLAND,SCH MED,CANC RES LAB,AUCKLAND,NEW ZEALAND
[2] UNIV MELBOURNE,INST EDUC,SCH SCI & MATH EDUC,PARKVILLE,VIC 3052,AUSTRALIA
[3] VICTORIAN COLL PHARM,DEPT MED CHEM,PARKVILLE,VIC 3052,AUSTRALIA
关键词
D O I
10.1021/jm00094a008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of acridine-2- and -4-carboxamide-linked analogues of PtenCl2 has been prepared and evaluated for biological activity against several tumor cell lines in vitro and in vivo. The platinum complexes were generally more cytotoxic than the corresponding ligands against wild-type P388 leukemia cells in vitro, with acridine-4-carboxamide complexes being the more effective. In contrast to cisplatin and PtenCl2, the complexes were equally active in vitro against both wild-type and cisplatin-resistant P388 lines. The 4-carboxamide complexes showed high levels of in vivo activity (ILS >100%) against wild-type P388 using a single-dose protocol, and one compound was also significantly active in vivo in a cisplatin-resistant line, against which cisplatin and PtenCl2 are inactive.
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页码:2983 / 2987
页数:5
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