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ACS Chemical Biology|October 4, 2008
Vinylogous ureas as a novel class of inhibitors of reverse transcriptase-associated ribonuclease H activityMichaela Wendeler, Hsiu-Fang Lee, Alun Bermingham, et al.
Infectious Agents and Cancer|June 30, 2021
Comprehensive high-throughput meta-analysis of differentially expressed microRNAs in transcriptomic datasets reveals significant disruption of MAPK/JNK signal transduction pathway in Adult T-cell leukemia/lymphomaShahrzad Shadabi, Nargess Delrish, Mehdi Norouzi, et al.
Antimicrobial Agents and Chemotherapy|June 1, 2017
Nucleotide Substrate Specificity of Anti-Hepatitis C Virus Nucleoside Analogs for Human Mitochondrial RNA PolymeraseMaryam Ehteshami, Longhu Zhou, Sheida Amiralaei, et al.
Journal of Medicinal Chemistry|April 8, 2015
β-D-2'-C-Methyl-2,6-diaminopurine Ribonucleoside Phosphoramidates are Potent and Selective Inhibitors of Hepatitis C Virus (HCV) and Are Bioconverted Intracellularly to Bioactive 2,6-Diaminopurine and Guanosine 5'-Triphosphate FormsLonghu Zhou, Hong-wang Zhang, Sijia Tao, et al.
Journal of Medicinal Chemistry|June 9, 2017
2'-Chloro,2'-fluoro Ribonucleotide Prodrugs with Potent Pan-genotypic Activity against Hepatitis C Virus Replication in CultureShaoman Zhou, Sawsan Mahmoud, Peng Liu, et al.
Antiviral Research|November 27, 2013
Chutes and ladders in hepatitis C nucleoside drug developmentSteven J Coats, Ethel C Garnier-Amblard, Franck Amblard, et al.
Antimicrobial Agents and Chemotherapy|May 25, 2016
Biochemical Characterization of the Active Anti-Hepatitis C Virus Metabolites of 2,6-Diaminopurine Ribonucleoside Prodrug Compared to Sofosbuvir and BMS-986094Maryam Ehteshami, Sijia Tao, Tugba Ozturk, et al.
Journal of Medicinal Chemistry|January 18, 2019
Discovery of a Series of 2'-α-Fluoro,2'-β-bromo-ribonucleosides and Their Phosphoramidate Prodrugs as Potent Pan-Genotypic Inhibitors of Hepatitis C VirusSeema Mengshetti, Longhu Zhou, Ozkan Sari, et al.
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