Page last updated: 2024-08-25

sofosbuvir and 4'-azidocytidine

sofosbuvir has been researched along with 4'-azidocytidine in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chan, K; Chen, YL; Fenaux, M; Ghafar, NA; Gu, F; Hunziker, J; Lim, SP; Lin, X; Rao, R; Saunders, OL; Seh, CC; Shi, PY; Wang, G; Xu, H; Yokokawa, F; Zhong, W1
Behera, I; Beigelman, L; Chaudhuri, S; Deval, J; Dyatkina, N; Jekle, A; Jin, Z; Kinkade, A; Rajwanshi, VK; Smith, DB; Symons, JA; Tucker, K; Wang, G1
Bao, H; Bourne, N; Espiritu, C; Frick, DN; Furman, PA; Heck, JA; Julander, JG; Keilman, M; Lam, AM; Morrey, JD; Murakami, E; Nagarathnam, D; Niu, C; Otto, MJ; Ross, BS; Smee, DF; Sofia, MJ; Steuer, HM; Wang, P; Zennou, V1

Other Studies

3 other study(ies) available for sofosbuvir and 4'-azidocytidine

ArticleYear
Structure-activity relationship of uridine-based nucleoside phosphoramidate prodrugs for inhibition of dengue virus RNA-dependent RNA polymerase.
    Bioorganic & medicinal chemistry letters, 2018, 07-15, Volume: 28, Issue:13

    Topics: Antiviral Agents; Dengue Virus; Enzyme Inhibitors; Hep G2 Cells; Humans; Leukocytes, Mononuclear; Molecular Structure; Mononuclear Phagocyte System; Prodrugs; RNA-Dependent RNA Polymerase; Structure-Activity Relationship; Uridine Monophosphate

2018
Structure-activity relationship analysis of mitochondrial toxicity caused by antiviral ribonucleoside analogs.
    Antiviral research, 2017, Volume: 143

    Topics: Adenosine; Amides; Antiviral Agents; Cell Line; Cytidine; DNA-Directed RNA Polymerases; Guanosine Monophosphate; Humans; Inhibitory Concentration 50; Mitochondria; Mitochondrial Proteins; Nucleosides; Prodrugs; Protein Biosynthesis; Pyrazines; Ribonucleosides; RNA; RNA, Mitochondrial; Sofosbuvir; Structure-Activity Relationship; Transcription Initiation Site; Transcription, Genetic

2017
PSI-7851, a pronucleotide of beta-D-2'-deoxy-2'-fluoro-2'-C-methyluridine monophosphate, is a potent and pan-genotype inhibitor of hepatitis C virus replication.
    Antimicrobial agents and chemotherapy, 2010, Volume: 54, Issue:8

    Topics: Amides; Antiviral Agents; Cell Line, Tumor; Deoxyuracil Nucleotides; Enzyme Inhibitors; Genotype; Hepacivirus; Humans; Phosphoric Acids; Prodrugs; Replicon; RNA-Dependent RNA Polymerase; RNA, Viral; Viral Nonstructural Proteins; Virus Replication

2010