生物信息学
双腺苷
司他夫定
核苷
尿苷
胞苷
药理学
阿巴卡韦
核苷类似物
拉米夫定
化学
生物
生物化学
病毒学
酶
病毒
核糖核酸
基因
乙型肝炎病毒
作者
Sarkar M. A. Kawsar,Nasrin S. Munia,Supriyo Saha,Yasuhiro Ozeki
标识
DOI:10.2174/0113895575258033231024073521
摘要
Nucleoside analogs have been widely used as antiviral, antitumor, and antiparasitic agents due to their ability to inhibit nucleic acid synthesis. Adenosine, cytidine, guanosine, thymidine and uridine analogs such as didanosine, vidarabine, remdesivir, gemcitabine, lamivudine, acyclovir, abacavir, zidovusine, stavudine, and idoxuridine showed remarkable anticancer and antiviral activities. In our previously published articles, our main intention was to develop newer generation nucleoside analogs with acylation-induced modification of the hydroxyl group and showcase their biological potencies. In the process of developing nucleoside analogs,
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