SYNTHESIS, CHARACTERIZATION AND INVITRO ANTITUMOR-ACTIVITY OF DI-NORMAL-BUTYLTIN(IV) DERIVATIVES OF SOME AROMATIC CARBOXYLIC-ACIDS, INCLUDING ASPIRIN

被引:33
作者
MERIEM, A
WILLEM, R
BIESEMANS, M
MAHIEU, B
DEVOS, D
LELIEVELD, P
GIELEN, M
机构
[1] VRIJE UNIV BRUSSELS,DIENST AOSC,B-1050 BRUSSELS,BELGIUM
[2] VRIJE UNIV BRUSSELS,HOOG RESOLUTIE NMR CENTRUM,B-1050 BRUSSELS,BELGIUM
[3] CATHOLIC UNIV LOUVAIN,INAN,B-1348 LOUVAIN,BELGIUM
[4] PHARMACHEM BV,2003 RN HAARLEM,NETHERLANDS
[5] TNO,CIVO INST,3700 AJ ZEIST,NETHERLANDS
[6] VRIJE UNIV BRUSSELS,DIENST ALGC,B-1050 BRUSSELS,BELGIUM
[7] UNIV LIBRE BRUXELLES,FAC SCI,B-1050 BRUSSELS,BELGIUM
[8] FAC SCI OUJDA,DEPT CHIM,OUJDA,MOROCCO
关键词
ORGANOTIN; NMR; ANTITUMOR; MOSSBAUER; MASS SPECTRUM; CARBOXYLATE;
D O I
10.1002/aoc.590050309
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Eleven di-n-butyltin(IV) derivatives of the type (a) (C4H9)2(XYC6H3COO)2Sn or (b) {[(C4H9)2(XYC6-H3COO)Sn]2O}2 (X, Y = H, 2-OH, compound la; H, 2-OCH3, compounds 2a and 2b; H, 2-OCOCH3, 3a; 2-OH, 3-OCH3, 4a; 2-OH, 3-CH3, 5a; H, 3-OCH3, 6a and 6b; H, 3-N(CH3)2, 7a; H, 2-(CF3), 5-(CF3), 8a and 3-OCH3, 4-OH, 9a) have been prepared and characterized by H-1, C-13 and Sn-119 NMR, Mossbauer and mass spectroscopy. The in vitro antitumour activity of these compounds against MCF-7 human tumour cells was higher than that of cis-platin, but only three compounds, 4a, 8a and 9a, scored better than cis-platin against the WiDr cell line.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 11 条
[1]  
BOUALAM M, 1990, APPL ORGANOMET CHEM, V4, P335
[2]  
BOUALAM M, IN PRESS HETEROATOM
[3]   SYNTHESIS, CHARACTERIZATION AND ANTITUMOUR ACTIVITY OF 7,7-DI-NORMAL-BUTYL-5,9-DIOXO-6,8-DIOXA-7-STANNA-SPIRO[3,5]NONANE, A DI-NORMAL-BUTYLTIN(IV) ANALOG OF PARAPLATIN, AND OF A SERIES OF DI-NORMAL-BUTYLTIN(IV) DERIVATIVES OF MONOSUBSTITUTED AND DISUBSTITUTED MALONIC-ACIDS [J].
GIELEN, M ;
MELOTTE, M ;
ATASSI, G ;
WILLEM, R .
TETRAHEDRON, 1989, 45 (04) :1219-1229
[4]  
GIELEN M, 1988, B SOC CHIM BELG, V97, P873
[5]  
KALINOWSKI HO, 1988, CARBON NMR SPECTROSC
[6]   SYNTHESIS, CHARACTERIZATION AND ANTITUMOUR ACTIVITY OF A SERIES OF DIORGANOTIN(IV) DERIVATIVES OF BIS(CARBOXYMETHYL)AMINES [J].
MERIEM, A ;
GIELEN, M ;
WILLEM, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1989, 365 (1-2) :91-101
[7]  
Meriem A., 1990, MAIN GROUP MET CHEM, V13, P167
[8]   STRUCTURAL CHEMISTRY OF ORGANOTIN CARBOXYLATES .4. SYNTHESIS AND SPECTROSCOPIC PROPERTIES OF DIORGANOTIN(IV) COMPLEXES WITH ORTHO-ANISIC ACID - THE CRYSTAL AND MOLECULAR-STRUCTURE OF ([NBU2SN(2-MEOC6H4COO)]2O)2 [J].
PARULEKAR, CS ;
JAIN, VK ;
KESAVADAS, T ;
TIEKINK, ERT .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1990, 387 (02) :163-173
[9]   STRUCTURAL CHEMISTRY OF ORGANOTIN CARBOXYLATES .2. THE CRYSTAL-STRUCTURE OF THE DICARBOXYLATO TETRAORGANODISTANNOXANE - ([NORMAL-BU2SN(O2CC5H4N)]2O)2 [J].
PARULEKAR, CS ;
JAIN, VK ;
DAS, TK ;
GUPTA, AR ;
HOSKINS, BF ;
TIEKINK, ERT .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1989, 372 (02) :193-199
[10]   STRUCTURAL CHEMISTRY OF ORGANOTIN CARBOXYLATES .1. THE CRYSTAL-STRUCTURE OF DI-NORMAL-BUTYLBIS(THIOPHENOXYACETATO)-TIN(IV)-NBU2SN(O2CCH2SC6H5)2 [J].
SANDHU, GK ;
SHARMA, N ;
TIEKINK, ERT .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1989, 371 (01) :C1-C3