The development of structurally novel nucleoside analogues is an active area in medicinal chemistry, since these drugs have proven clinical efficacy for decades. Azanucleosides are nucleoside analogues in which the sugar moieties are composed of nitrogen-containing rings or chains. In recent years, many azanucleosides have demonstrated therapeutic potential. In this short review, we describe recent advancements in azanucleosides, which may translate in a better understanding of the molecular design, biological activity, structure–activity relationship, and their related mechanism of action. The information summarized in this paper should encourage medicinal chemists in their future efforts to create more potent and effective chemotherapeutic agents.
CITATION STYLE
Zhang, Y., Geng, H., Zhang, J., & He, K. (2022, July 1). An Update Mini-Review on the Progress of Azanucleoside Analogues. Chemical and Pharmaceutical Bulletin. Pharmaceutical Society of Japan. https://doi.org/10.1248/cpb.c22-00088
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