Nucleoside analog drugs

Valacyclovir is an antiviral drug that belongs to the purine (guanine) nucleoside analog drug class.¹. As a prodrug to acyclovir (Zovirax)

analogs into medicines. The company, through its technology, is purine and pyrimidine-based nucleosides as potential drug candidates. The

Drug resistance to acyclovir and Acyclovir, famciclovir, and valacyclovir are antiviral agents within the nucleoside analog class.

by A Fyrberg 2024nucleoside analog cytotoxicity, making these drugs rather nonspecific in their target. Some nucleoside analogs are however active in non- proliferating

Nucleoside Metabolism is the Key to Understanding the Mechanism of Action of Nucleoside Drugs. Unlike most drugs, nucleosides and their analogs in the human body are first exposed to a number of enzymes of cellular metabolism, which convert them into active forms (nucleotides).

6. Nucleoside Analogs as Anti-HCoV Drugs. Nucleoside analogs are widely used as drugs against infections caused by herpes viruses, hepatitis B virus, human immunodeficiency virus (HIV) but also against RNA virus infections such as hepatitis C .

Nucleoside/nucleotide reverse transcriptase inhibitors, also called nucleoside analogs, such as abacavir, emtricitabine, and tenofovir. These medicines are

Acyclovir belongs to a group of synthetic drugs called nucleoside analogs, which are characterized by their similarity to naturally occurring

Nucleoside/nucleotide reverse transcriptase inhibitors, also called nucleoside analogs, such as abacavir, emtricitabine, and tenofovir. These medicines are