Pressová M, Endová M, Toĉík Z, Liboska R, Rosenberg I
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague.
Bioorg Med Chem Lett. 1998 May 19;8(10):1225-30. doi: 10.1016/s0960-894x(98)00190-5.
The isopolar nonisosteric phosphonate analogs of ApA differing in the position of extra methylene group introduced into the sugar-phosphate backbone, featuring both possible 2',5'- and 3',5'- pairs as well as their conformationally restricted congeners, were investigated for their ability to form complexes with polyU. The results may lead to the specification of candidates for synthesis of novel oligonucleotides.
研究了ApA的等极性非等排膦酸酯类似物,这些类似物在引入糖磷酸主链的额外亚甲基位置上有所不同,具有可能的2',5'-和3',5'-对以及它们的构象受限同系物,考察了它们与聚U形成复合物的能力。这些结果可能有助于确定新型寡核苷酸合成候选物的具体情况。