Synthesis and antiproliferative activity of some thiazolylbenzimidazole-4,7-diones

被引:35
作者
Garuti, L
Roberti, M
Pession, A
Leoncini, E
Hrelia, S
机构
[1] Univ Bologna, Dept Pharmaceut Sci, I-40126 Bologna, Italy
[2] Univ Bologna, Dept Expt Pathol, Bologna, Italy
[3] Univ Bologna, Dept Biochem G Morozzi, I-40126 Bologna, Italy
关键词
D O I
10.1016/S0960-894X(01)00639-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Some thiazolylbenzimidazole-4,7-diones were synthesized and tested in vitro on two tumor cell lines. Compounds 2d and 2e show a very good activity on K562 cells, whereas compounds 2a and 2b are active on SW620 cells. The importance of the methoxy group on the quinone moiety is confirmed and the function at 4-position of the thiazole ring plays a determining role for the activity. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3147 / 3149
页数:3
相关论文
共 13 条
[1]   Synthesis and cytotoxicity of analogues of the antibiotic BE 10988 inhibitors of DNA topoisomerase II [J].
Catrycke, MO ;
Houssin, R ;
Hénichart, JP ;
Pfeiffer, B ;
Renard, P ;
Dassonneville, L ;
Bailly, C .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1999, 9 (14) :2025-2030
[2]   Synthesis and antiproliferative activity of some benzimidazole-4,7-dione derivatives [J].
Garuti, L ;
Roberti, M ;
Malagoli, M ;
Rossi, T ;
Castelli, M .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (19) :2193-2195
[3]   Concentration- and time-dependent effects of γ-linolenic acid supplementation to tumor cells in culture [J].
Hrelia, S ;
Pession, A ;
Buda, R ;
Lorenzini, A ;
Horrobin, DF ;
Biagi, PL ;
Bordoni, A .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1999, 60 (04) :235-241
[4]   gamma-linolenic acid supplementation can affect cancer cell proliferation via modification of fatty acid composition [J].
Hrelia, S ;
Bordoni, A ;
Biagi, P ;
Rossi, CA ;
Bernardi, L ;
Horrobin, DF ;
Pession, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (02) :441-447
[5]  
HRELIA S, 1994, BIOCHEM MOL BIOL INT, V34, P449
[6]  
MASOTTI L, 1988, FREE RADICAL BIO MED, V4, P337
[7]   SYNTHESIS OF THE TOPOISOMERASE-II INHIBITOR BE-10988 [J].
MOODY, CJ ;
SWANN, E .
TETRAHEDRON LETTERS, 1993, 34 (12) :1987-1988
[8]   SYNTHESIS AND BIOLOGICAL-ACTIVITY OF THIAZOLYLINDOLEQUINONES, ANALOGS OF THE NATURAL PRODUCT BE-10988 [J].
MOODY, CJ ;
SWANN, E ;
HOULBROOK, S ;
STEPHENS, MA ;
STRATFORD, IJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (06) :1039-1043
[9]  
MOODY CJ, J CHEM SOC P1, P2561
[10]   A NEW TOPOISOMERASE-II INHIBITOR, BE-10988, PRODUCED BY A STREPTOMYCETE .1. TAXONOMY, FERMENTATION, ISOLATION AND CHARACTERIZATION [J].
OKA, H ;
YOSHINARI, T ;
MURAI, T ;
KAWAMURA, K ;
SATOH, F ;
FUNAISHI, K ;
OKURA, A ;
SUDA, H ;
OKANISHI, M ;
SHIZURI, Y .
JOURNAL OF ANTIBIOTICS, 1991, 44 (05) :486-491