کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1317968 | 976620 | 2010 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Dinuclear triphenylphosphinegold(I) sulfanylcarboxylates: Synthesis, structure and cytotoxic activity against cancer cell lines Dinuclear triphenylphosphinegold(I) sulfanylcarboxylates: Synthesis, structure and cytotoxic activity against cancer cell lines](/preview/png/1317968.png)
Compounds of the type [(AuPPh3)2(xspa)]; H2xspa [x:p = 3-phenyl-, f = 3-(2-furyl)-, t = 3-(2-thienyl)-, -o-py = 3-(2-pyridyl)-, Clp = 3-(2-chlorophenyl)-, -o-mp = 3-(2-methoxyphenyl)-, -p-mp = 3-(4-methoxyphenyl)-, -o-hp = 3-(2-hydroxyphenyl)-, -p-hp = 3-(4-hydroxyphenyl)-, -diBr-o-hp = 3-(3,5-dibromo-2-hydroxyphenyl)-; spa = 2-sulfanyl propenoato] were synthesized and characterized by IR and NMR (1H, 13C and 31P) spectroscopy and by FAB mass spectrometry. The structures of [(AuPPh3)2(Clpspa)], [(AuPPh3)2(o-hpspa)], [(AuPPh3)2(p-hpspa)]·MeOH and [(AuPPh3)2(diBr-o-hpspa)]·2Me2CO show the dinuclear nature of the complexes with the two gold atoms, one of which is also O-bonded to an O atom of the carboxylate group, bonded to the S atom. The in vitro antitumor activities against the HeLa-229, A2780 and A2780cis cell lines were determined and the compounds were found to be highly effective, in particular against the A2780cis cell line, with eight of the nine compounds having IC50 values better than that of cisplatin. This behavior is indicative of a high ability to circumvent the cellular resistance to this drug.
The reaction of 3-(aryl)-2-sulfanylpropenoic acids (H2xspa), with triphenylphosphinegold(I) chloride in basic media afforded complexes of the type [(AuPPh3)2xspa]. The structures show a dinuclear nature for the complexes, which show significant invitro antitumor activities, in particular against the A2780cis cell line, indicative of a high ability to circumvent the cellular resistance to cisplatin.Figure optionsDownload as PowerPoint slide
Journal: Journal of Inorganic Biochemistry - Volume 104, Issue 5, May 2010, Pages 551–559