Diorganotin(IV) complexes of pyridoxal thiosemicarbazone:: Synthesis, spectroscopic properties and biological activity

被引:39
|
作者
Casas, JS [1 ]
Rodríguez-Argüelles, MC
Russo, U
Sánchez, A
Sordo, J
Vázquez-López, A
Pinelli, S
Lunghi, P
Bonati, A
Albertini, R
机构
[1] Univ Santiago de Compostela, Fac Farm, Dept Quim Inorgan, Santiago De Compostela 15706, Spain
[2] Univ Vigo, Dept Quim Inorgan, Vigo 36200, Spain
[3] Univ Padua, Dipartimento Chim Inorgan Metallorgan & Analit, I-35131 Padua, Italy
[4] Univ Parma, Ist Patol Speciale Med, I-43100 Parma, Italy
[5] Univ Parma, Ctr Ric Interuniv Diag Terapia & Prognosi Tumori, I-43100 Parma, Italy
关键词
diorganotine complexes; pyridoxal thiosemicarbazone complexes; biological activity studies;
D O I
10.1016/S0162-0134(98)00004-X
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
The complexes [SnR2(L)] (R = Me, Et, Bu, Ph; H2L = pyridoxal thiosemicarbazone) have been prepared and characterized. In the light of the spectral properties of the complexes in the solid state (IR, mass, Mossbauer) the bideprotonated thiosemicarbazonato anion is O(phenolic)-, N(3)-, S-bonded to the tin atom which probably has trigonal bipyramidal coordination with N(3) atom and R groups occupying equatorial positions. NMR(H-1, C-13 and Sn-119) data in CDCl3 or DMSO-d(6) suggest that this coordinative picture remains in these solutions. The ethyl, butyl and phenyl derivatives suppress proliferation of Friend erithroleukaemia cells (FLC), Of the pyridoxal thiosemicarbazone complexes so far evaluated, [SnBu2(L)] and [SnPh2(L)] showed the lowest thresholds for inhibition of FLC proliferation. The effects of these compounds on DMSO-induced differentiation of FLC, DNA synthesis and reverse transcriptase were also assayed. (C) 1998 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:283 / 292
页数:10
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