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[ASAP] Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase
(Journal of Medicinal Chemistry)
20 april 2019 03:00:29
[ASAP] Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase
(Journal of Medicinal Chemistry)
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Journal of Medicinal ChemistryDOI: 10.1021/acs.jmedchem.9b00020
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[ASAP] Development of Novel Epoxyketone-Based Proteasome Inhibitors as a Strategy To Overcome Cancer Resistance to Carfilzomib and Bortezomib
(Journal of Medicinal Chemistry)
[ASAP] Synthesis and Anti-HCV Activities of 4`-Fluoro-2`-Substituted Uridine Triphosphates and Nucleotide Prodrugs: Discovery of 4`-Fluoro-2`-C-methyluridine 5`-Phosphoramidate Prodrug (AL-335) for the Treatment of Hepatitis C Infection
(Journal of Medicinal Chemistry)
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