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Cytotoxicity of New N-butylamino and Sulfur-containing Derivatives of Polyfluorinated 1,4-Naphthoquinone by Ol'ga A. Zakharova; Leonid I. Goryunov; Nadezhda M. Troshkova; Ludmila P. Ovchinnikova; Vitalij D. Shteingarts; Georgy A. Nevinsky is a Chemistry article available to read on EtoBox.
What is Cytotoxicity of New N-butylamino and Sulfur-containing Derivatives of Polyfluorinated 1,4-Naphthoquinone about?
a b s t r a c t Four new n-butylamino and two sulfur-containing derivatives of polyfluoro-1,4-naphthoquinone were synthesized and their mutagenic and antioxidant properties in Salmonella cells, as well as the cytotoxicity in human myeloma (RPMI 8226), human mammary adenocarcinoma (MCF-7), mouse fibroblasts (LMTK) and primary mouse fibroblast cells (PMF) were studied. 2-n-Butylamino-3,5,6,7,8-pentafluoro-1,4-naphthoquinone (1) showed efficient inhibition of the growth of the tumor cells. 2,8-Di-(n-butylamino)-3,5,6,7-tetrafluoro-1,4-naphthoquinone (2) had significantly less growth-inhibiting properties, while 2,6-di-(n-butylamino)-3,5,7,8-tetrafluoro-1,4-naphthoquinone (3) and 2,6,8-tri-(n-butylamino)-3,5,7-tetrafluoro-1,4-naphthoquinone (4), demonstrated very low cytotoxicity. Compounds 1 and 2 were remarkably less cytotoxic while compound 3 and 4 were not cytotoxic toward LMTK and PMF cells as compared with tumor human cell lines. Cytotoxicity of 2-(2 0 -methylthioethyl)amino-3,5,6,7,8-pentafluoro-1,4-naphthoquinone (5) and (2,2 0 -dithiodi-2)-3,5,6,7,8-pentafluoro-1,4-naphthoquinone-2-ylamino)ethan (6) toward mammalian cells was compared with that for compounds 1 and 2.
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- Author
- Ol'ga A. Zakharova; Leonid I. Goryunov; Nadezhda M. Troshkova; Ludmila P. Ovchinnikova; Vitalij D. Shteingarts; Georgy A. Nevinsky
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0223-5234)
- Published
- 2010
- Language
- EN
- Field
- Chemistry (Physical Sciences)