Abramova T V, Vlasov V V, Ivanova E M, Zarytova V F, Fokina T N, Frolova E I, Iurchenko L V
Mol Biol (Mosk). 1994 Mar-Apr;28(2):307-12.
Inhibition of the influenza virus protein NP mRNA with derivatives of an antisense oligonucleotide complementary to the 5' terminus of the mRNA was investigated. The derivatives were prepared by conjugation of aromatic 2-chloroethylamine, cholesterol, porphyrin, and phenazine groups to the 5'-terminal phosphate of the oligonucleotide. The most efficient inhibitors were found to be the conjugates bearing the alkylating, cholesterol and phenaznium groups.
研究了用与流感病毒蛋白NP mRNA 5'末端互补的反义寡核苷酸衍生物抑制该mRNA的情况。这些衍生物是通过将芳香族2-氯乙胺、胆固醇、卟啉和吩嗪基团与寡核苷酸的5'-末端磷酸基团偶联而制备的。发现最有效的抑制剂是带有烷基化基团、胆固醇基团和吩嗪鎓基团的偶联物。