Flexibility-Not just for yoga anymore!

Q2 Pharmacology, Toxicology and Pharmaceutics Antiviral Chemistry and Chemotherapy Pub Date : 2018-01-01 DOI:10.1177/2040206618756788
Katherine Seley-Radtke
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引用次数: 7

Abstract

Over the past few years, nucleosides have maintained a prominent role as one of the cornerstones of antiviral and anticancer therapeutics, and many approaches to nucleoside drug design have been pursued. One such approach involves flexibility in the sugar moiety of nucleosides, for example, in the highly successful anti-HIV and HBV drug tenofovir. In contrast, introduction of flexibility to the nucleobase scaffold has only more recently gained significance with the invention of our fleximers. The history, development, and some biological relevance for this innovative class of nucleosides are detailed herein.

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灵活性——不再是瑜伽的专利!
在过去的几年中,核苷作为抗病毒和抗癌治疗的基石之一保持着突出的作用,许多核苷药物设计的方法已经被追求。其中一种方法涉及核苷糖部分的灵活性,例如在非常成功的抗hiv和HBV药物替诺福韦中。相比之下,引入核碱基支架的灵活性直到最近才随着我们的柔韧剂的发明而获得意义。本文详细介绍了这类创新核苷的历史、发展和一些生物学意义。
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来源期刊
Antiviral Chemistry and Chemotherapy
Antiviral Chemistry and Chemotherapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.20
自引率
0.00%
发文量
5
审稿时长
15 weeks
期刊介绍: Antiviral Chemistry & Chemotherapy publishes the results of original research concerned with the biochemistry, mode of action, chemistry, pharmacology and virology of antiviral compounds. Manuscripts dealing with molecular biology, animal models and vaccines are welcome. The journal also publishes reviews, pointers, short communications and correspondence.
期刊最新文献
The continuing need for therapeutic agents for respiratory syncytial virus infection. The development of BVDU: An odyssey. Meeting report: 34th international conference on antiviral research. Active site polymerase inhibitor nucleotides (ASPINs): Potential agents for chronic HBV cure regimens. Reflections on the Rega Institute for Medical Research, at the fiftieth anniversary of the Rega Stichting vzw (Rega Instituut vzw, Rega Foundation).
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