O'Connor T E
Ann N Y Acad Sci. 1977 Mar 4;284:544-65. doi: 10.1111/j.1749-6632.1977.tb21987.x.
Thirteen rifamycin SV derivatives containing 3'-alkylaminomethyl substituents fail to inhibit the activities of the simian sarcoma virus Type 1 DNA polymerase, and of cellular DNA, RNA, and poly(A) polymerases prepared from NIH Swiss mouse embryos. These compounds show a range in their toxicities for NIH Swiss mouse 3T3 cells and in their capacities to inhibit production of foci of morphologically altered cells by murine sarcoma virus (MSV). Three compounds--the N-methyl-N-hydroxyethylaminomethyl, the N,N-dimethyl-aminomethyl, and the N4-methylpiperazinomethyl rifamycin derivatives--are comparable to adenine arabinoside and ribavirin in their toxicity for 3T3 cells, but these compounds show superior focus inhibition. These compounds inhibit oncornavirus production apparently by exacerbation of a delay in growth that results from infection of 3T3 cells with MSV.
13种含有3'-烷基氨甲基取代基的利福霉素SV衍生物不能抑制1型猿猴肉瘤病毒DNA聚合酶以及从NIH瑞士小鼠胚胎制备的细胞DNA、RNA和聚(A)聚合酶的活性。这些化合物对NIH瑞士小鼠3T3细胞的毒性以及抑制鼠肉瘤病毒(MSV)产生形态改变细胞集落的能力各不相同。三种化合物——N-甲基-N-羟乙氨甲基、N,N-二甲基氨甲基和N4-甲基哌嗪甲基利福霉素衍生物——对3T3细胞的毒性与阿糖腺苷和利巴韦林相当,但这些化合物在抑制集落形成方面表现更优。这些化合物显然是通过加剧MSV感染3T3细胞导致的生长延迟来抑制肿瘤病毒的产生。