Synthesis and biological evaluation of 3-arylisoquinolines as antitumor agents

被引:49
作者
Cho, WJ [1 ]
Park, MJ
Chung, BH
Lee, CO
机构
[1] Chonnam Natl Univ, Coll Pharm, Kwangju 500757, South Korea
[2] Korea Res Inst Chem Technol, Screening Ctr, Daejeon, South Korea
关键词
D O I
10.1016/S0960-894X(97)10190-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
To investigate the structure-activity relationship of 7,8-dimethoxy-2-methyl-3-(4,5-methylenedioxy-2-vinylphenyl)isoquinolin-1(2H)-one 2, diverse substituted 3-arylisoquinolines were synthesized and tested in vitro antitumor activity against five human tumor cell lines. The results showed a broad antitumor spectrum for a series of 3-arylisoquinolines. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:41 / 46
页数:6
相关论文
共 13 条
[1]  
14 CONV NAZ DIV CHIM, 1992, Patent No. 487930
[2]  
BEHRENS CH, 1990, Patent No. 4942163
[3]   THIONATION REACTIONS OF LAWESSON REAGENTS [J].
CAVA, MP ;
LEVINSON, MI .
TETRAHEDRON, 1985, 41 (22) :5061-5087
[4]   Synthesis of benzo[c]phenanthridine derivatives and their in vitro antitumor activities [J].
Cho, WJ ;
Yoo, SJ ;
Chung, BH ;
Choi, BG ;
Cheon, SH ;
Whang, SH ;
Kim, SK ;
Kang, BH ;
Lee, CO .
ARCHIVES OF PHARMACAL RESEARCH, 1996, 19 (04) :321-325
[5]   INHIBITORS OF DNA TOPOISOMERASE-I ISOLATED FROM THE ROOTS OF ZANTHOXYLUM-NITIDUM [J].
FANG, SD ;
WANG, LK ;
HECHT, SM .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (19) :5025-5027
[6]   SYNTHESIS AND EVALUATION OF NEW 6-AMINO-SUBSTITUTED BENZO[C]PHENANTHRIDINE DERIVATIVES [J].
JANIN, YL ;
CROISY, A ;
RIOU, JF ;
BISAGNI, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (23) :3686-3692
[7]  
KOBAYASHI F, 1992, Patent No. 04364128
[8]  
Mackay SP, 1997, ADV HETEROCYCL CHEM, V67, P345
[9]  
ONDA M, 1979, CHEM PHARM BULL, V27, P2076
[10]   CONVENIENT PREPARATION OF 3-SUBSTITUTED 1(2H)-ISOQUINOLINONES [J].
POINDEXTER, GS .
JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (19) :3787-3788