The present disclosure describes tetrahydropyran nucleoside analogs, oligomeric compounds prepared therefrom and methods of using the oligomeric compounds. More particularly, novel tetrahydropyran nucleoside analogs are provided having at least one chiral substituent that are expected to be useful for enhancing one or more properties of oligomeric compounds such as nuclease resistance and/or binding affinity. In certain embodiments, the oligomeric compounds are expected to hybridize to a portion of a target RNA resulting in loss of normal function of the target RNA.
本公开说明描述了
四氢吡喃核苷类似物,以及从中制备的寡聚化合物和使用寡聚化合物的方法。更具体地,提供了具有至少一个手性取代基的新型
四氢吡喃核苷类似物,预计对增强寡聚化合物的一个或多个性质(如
核酸酶抗性和/或结合亲和力)有用。在某些实施例中,预计寡聚化合物将杂交到目标RNA的一部分,导致目标RNA失去正常功能。