Sanyal U, Chatterjee R S, Das S K, Chakraborti S K
Neoplasma. 1984;31(2):149-55.
A series of twenty-four alkylphosphonium salts were prepared and evaluated as potential antitumor agents in vivo against Ehrlich ascites carcinoma (EAC). Eleven compounds were screened in vivo against lymphoid leukemia L1210 and one against lymphocytic leukemia P388. Out of these, three compounds exhibited mild antitumor activity against EAC. Twenty compounds were tested for their cytotoxic activity against the growth of tissue culture cells originated from human epidermoid carcinoma of the nasopharynx (KB). All compounds but one exhibited significant cytotoxicity in this cell line. 2-Bromoethyltriphenylphosphonium bromide, chosen as a standard compound, was earlier reported [4] to have borderline activity against P388, but it failed to show any activity against EAC though it has exhibited significant in vitro cytotoxicity in KB cell culture. In the course of this study, seven new alkylphosphonium salts were synthesized.
制备了一系列24种烷基鏻盐,并在体内评估其作为抗艾氏腹水癌(EAC)潜在抗肿瘤药物的活性。对11种化合物进行了抗淋巴细胞白血病L1210的体内筛选,对1种化合物进行了抗淋巴细胞白血病P388的体内筛选。其中,3种化合物对EAC表现出轻度抗肿瘤活性。测试了20种化合物对源自人鼻咽表皮样癌(KB)的组织培养细胞生长的细胞毒性活性。除一种化合物外,所有化合物在该细胞系中均表现出显著的细胞毒性。作为标准化合物选择的2-溴乙基三苯基溴化鏻, earlier reported [4] 对P388具有临界活性,但尽管它在KB细胞培养中表现出显著的体外细胞毒性,但对EAC未显示任何活性。在本研究过程中,合成了7种新的烷基鏻盐。