Nair V, Jahnke T S
Department of Chemistry, University of Iowa, Iowa City 52242, USA.
Antimicrob Agents Chemother. 1995 May;39(5):1017-29. doi: 10.1128/AAC.39.5.1017.
In summary, many isomeric analogs of ddNs of both D-related and L-related absolute stereochemistries have been synthesized and evaluated in vitro for their antiviral activities. A few of these compounds exhibit potent antiviral activity and, interestingly, belong to both the D and L families. The synthetic methodologies developed will allow accessibility to many more novel modified nucleosides. While some structure-activity relationships are emerging from this work, it is clear that these chiral isomeric nucleosides have opened a new chapter in the field of antiviral nucleosides.
总之,已经合成了许多具有D型和L型绝对立体化学的ddN的异构类似物,并在体外评估了它们的抗病毒活性。其中一些化合物表现出强大的抗病毒活性,有趣的是,它们分属于D族和L族。所开发的合成方法将有助于获得更多新型修饰核苷。虽然这项工作中出现了一些构效关系,但很明显,这些手性异构核苷在抗病毒核苷领域开启了新的篇章。