Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity

被引:103
作者
Choi, SJ
Park, HJ
Lee, SK
Kim, SW
Han, G
Choo, HYP [1 ]
机构
[1] Ewha Womans Univ, Sch Pharm, Seoul 120750, South Korea
[2] Leadgenex Inc, Taejon 306230, South Korea
[3] Yonsei Univ, Dept Biotechnol, Seoul 120749, South Korea
关键词
benzothiazoles; solid phase synthesis; topoisomerase II; inhibitory activity; cytotoxicity;
D O I
10.1016/j.bmc.2005.09.051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate one possible mechanism of action of the cytotoxic activity of benzothiazoles, we synthesized 2-(substituted-phenyl)benzothiazoles and evaluated their ability to inhibit topoisomerase 11 activities. Solid phase combinatorial method using trityl resin was employed and benzothiazole derivatives with Various substitution on 2'-, 3'-, or 4'-position of phenyl group were obtained in ca. 30 mg scale (7-96% yield). Most of the compounds synthesized exhibited topoisomerase 11 inhibitory activity at 100 mu M. 2-(3-Amino-4-methylphenyl)benzothiazole showed high activity (IC50 = 71.7 mu M), comparable to etoposide (IC50 = 78.4 mu M). (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1229 / 1235
页数:7
相关论文
共 14 条
[1]   Mechanism of action of eukaryotic topoisomerase II and drugs targeted to the enzyme [J].
Burden, DA ;
Osheroff, N .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1400 (1-3) :139-154
[2]   Antitumor benzothiazoles. 7. Synthesis of 2-(4-acylaminophenyl)benzothiazoles and investigations into the role of acetylation in the antitumor activities of the parent amines [J].
Chua, MS ;
Shi, DF ;
Wrigley, S ;
Bradshaw, TD ;
Hutchinson, I ;
Shaw, PN ;
Barrett, DA ;
Stanley, LA ;
Stevens, MFG .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (03) :381-392
[3]  
GOLDFARB RH, 2000, Patent No. 6013659
[4]  
HUCTCHISON I, 2001, J MED CHEM, V44, P1446
[5]   Synthesis, cytotoxicity, DNA interaction and topoisomerase II inhibition properties of tetrahydropyrrolo[3,4-a]carbazole-1,3-dione and tetrahydropyrido-[3,2-b]pyrrolo[3,4-g]indole derivatives [J].
Joseph, B ;
Facompré, M ;
Da Costa, H ;
Routier, S ;
Mérour, JY ;
Colson, P ;
Houssier, C ;
Bailly, C .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (06) :1533-1541
[6]   Antitumor benzothiazoles.: 8.: Synthesis, metabolic formation, and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl)benzothiazoles [J].
Kashiyama, E ;
Hutchinson, I ;
Chua, MS ;
Stinson, SF ;
Phillips, LR ;
Kaur, G ;
Sausville, EA ;
Bradshaw, TD ;
Westwell, AD ;
Stevens, MFG .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (20) :4172-4184
[7]   Cytostatic mechanism and antitumor potential of novel 1H-cyclopenta[b]benzofuran lignans isolated from Aglaia elliptica [J].
Lee, SK ;
Cui, B ;
Mehta, RR ;
Kinghorn, AD ;
Pezzuto, JM .
CHEMICO-BIOLOGICAL INTERACTIONS, 1998, 115 (03) :215-228
[8]   Solid phase synthesis of benzothiazolyl compounds [J].
Mourtas, S ;
Gatos, D ;
Barlos, K .
TETRAHEDRON LETTERS, 2001, 42 (11) :2201-2204
[9]   Genotoxicity of the laxative drug components emodin, aloe-emodin and danthron in mammalian cells: Topoisomerase II mediated? [J].
Muller, SO ;
Eckert, I ;
Lutz, WK ;
Stopper, H .
MUTATION RESEARCH-GENETIC TOXICOLOGY, 1996, 371 (3-4) :165-173
[10]   Some fused heterocyclic compounds as eukaryotic topoisomerase II inhibitors [J].
Pinar, A ;
Yurdakul, P ;
Yildiz, I ;
Temiz-Arpaci, O ;
Acan, NL ;
Aki-Sener, E ;
Yalcin, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 317 (02) :670-674