Fusková A, Proksa B, Fuska J
Pharmazie. 1977 May;32(5):291-3.
The effect was studied of 32 natural and synthetic derivatives of coumarin, dicoumarin, and 4.4'epoxydicoumarin on the uptake of 14C-labelled precursors in nucleic acid (NA) and protein synthesis by EAC cells in vitro. Of the three tested groups of compounds, the most cytotoxic effect was found in the derivatives of coumarin that inhibited, on the same level, incorporation of the added 14C-adenine, 14C-L-valine and 14C-uridine but not 14C-thymidine. The utilization of the present precursors by EAC cells was not affected by epoxydicoumarins. Derivatives of coumarin and dicoumarin inhibited only NA synthesis in in vitro proliferating EAC cells. Of the evaluated compounds, chiefly duclauxin specifically decreased proliferation of EAC cells in vitro.
研究了香豆素、双香豆素和4,4'-环氧双香豆素的32种天然和合成衍生物对体外培养的艾氏腹水癌细胞(EAC细胞)摄取14C标记的前体物质用于核酸(NA)和蛋白质合成的影响。在测试的三组化合物中,香豆素衍生物的细胞毒性作用最强,它们对添加的14C-腺嘌呤、14C-L-缬氨酸和14C-尿苷的掺入有同等程度的抑制作用,但对14C-胸腺嘧啶无抑制作用。环氧双香豆素不影响EAC细胞对这些前体物质的利用。香豆素和双香豆素的衍生物仅抑制体外增殖的EAC细胞中的NA合成。在所评估的化合物中,主要是杜克洛辛能特异性降低EAC细胞在体外的增殖。