Wilson R G, Kalonaros V, King M, Lockwood R, McNeill M
Chem Biol Interact. 1981 Nov;37(3):351-63. doi: 10.1016/0009-2797(81)90120-4.
Adriamycin and 4'-epi-adriamycin were compared as to their effect on nRNA synthesis. 4'-Epi-adriamycin was a more effective inhibitor than the parent compound of RNA synthesis as measured by incorporation of [3H]-uridine. Adriamycin inhibited all three species of nRNA (ribosomal, non-poly(A)hnRNA, poly(A)hnRNA) to approximately the same extent. 4'-Epi-adriamycin on the other hand inhibited the nRNA species in the following order: non-poly(A)hnRNA greater than ribosomal RNA greater than poly(A)hnRNA. The inhibitory effects of both drugs on incorporation of uridine into RNA were reversible at low concentrations (5 microgram/ml).
比较了阿霉素和4'-表阿霉素对核RNA合成的影响。通过[3H] -尿苷掺入法测定,4'-表阿霉素是比母体化合物更有效的RNA合成抑制剂。阿霉素对所有三种核RNA(核糖体RNA、非聚腺苷酸核不均一RNA、聚腺苷酸核不均一RNA)的抑制程度大致相同。另一方面,4'-表阿霉素对核RNA种类的抑制顺序如下:非聚腺苷酸核不均一RNA>核糖体RNA>聚腺苷酸核不均一RNA。两种药物在低浓度(5微克/毫升)时对尿苷掺入RNA的抑制作用都是可逆的。