Synthesis, structure and antitumor activity of dibutyltin oxide complexes with 5-fluorouracil derivatives. Crystal structure of [(5-fluorouracil)-1- CH2CH2COOSn(n-Bu)2]4O2

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Abstract

Dibutyltin (IV) oxide complex reacts with the fluorouracil compounds 5-fluorouracil-1-propanonic or 5-fluorouracil-1-acetic acid (Fu) to give the complexes [(5-Fu)-1-(CH2)nCOOSn(n-Bu)2] 4O2 (I, n=2; II, n=1) which were characterized by IR and 1H-NMR. The crystal structure of complex I shows that the molecular is a dimer, in which two [(5-Fu)-1-CH2CH2COOSn(n-Bu) 2]2O units are linked by a bridging oxygen atom, and the tin atoms adopt distorted trigonal bipyramids via two carbons from a dibutyl moiety and three oxygen atoms from 5-Fu and bridging oxygen. These complexes have potential anti-tumour activity: in vitro tests showed that complexes I and II exhibit high cytotoxicity against OVCAR-3 and PC-14.

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Zuo, D. S., Jiang, T., Guan, H. S., Wang, K. Q., Qi, X., & Shi, Z. (2001). Synthesis, structure and antitumor activity of dibutyltin oxide complexes with 5-fluorouracil derivatives. Crystal structure of [(5-fluorouracil)-1- CH2CH2COOSn(n-Bu)2]4O2. Molecules, 6(8), 647–654. https://doi.org/10.3390/60800647

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