作者:Diane M. Coe、Hans Hilpert、Stewart A. Noble、Michael R. Peel、Stanley M. Roberts、Richard Storer
DOI:10.1039/c39910000312
日期:——
The nucleotide analogues 10, 13, 14 and 20 have been synthesised; the latter phosphonate was converted into the diphosphoryl-phosphonate 21 and this compound was shown to be a potent inhibitor of HIV-coded reverse transcriptase.
核苷酸类似物 10、13、14 和 20 已被合成;后一种膦酸盐被转化为二磷酸膦酸盐 21,该化合物已被证明是艾滋病毒编码逆转录酶的强效抑制剂。