Stivala F, Bonina F, Iacona G, Cordopatri F, Mazzone G
Boll Soc Ital Biol Sper. 1978 Jul 30;54(14):1264-70.
The behaviour of alkaline salts of some aroyl-hydrazine-carbodithioic acids [comp. Ia,b,c,] and derivatives of 1,3,4-oxadiazole [comp. IIa,b,c, e IIIa,b,c] , has been studied, on the capability of lymphoblasts in vitro, in consequence of stimulation by some mitogen agents (PHA, PWM). It has been pointed out that the considered compounds inhibit the cellular mitosis in variable percentage in relation to their structure and to the used mitogen agent, frequently causing some mitogen-like morphological modification, also revealable under a optical microscope. The higher inhibition has been obtained by the Ic, IIc, and IIIc compounds, in which Ar is the 3,4-dihydroxymethylenephenyl radical, proving selective, in some cases, for the T lymphocytes.
研究了某些芳酰肼基二硫代碳酸的碱性盐[化合物Ia、b、c]以及1,3,4-恶二唑的衍生物[化合物IIa、b、c和IIIa、b、c]对体外淋巴细胞在某些促有丝分裂剂(PHA、PWM)刺激下的作用。已经指出,所考虑的化合物根据其结构和所用促有丝分裂剂的不同,以不同百分比抑制细胞有丝分裂,经常引起一些类似促有丝分裂剂的形态学改变,在光学显微镜下也可观察到。化合物Ic、IIc和IIIc获得了较高的抑制率,其中Ar为3,4-二羟基亚甲基苯基,在某些情况下对T淋巴细胞具有选择性。