Structure-Guided Synthesis and Mechanistic Studies Reveal Sweetspots on Naphthyl Salicyl Hydrazone Scaffold as Non-Nucleosidic Competitive, Reversible Inhibitors of Human Ribonucleotide Reductase

Journal of Medicinal ChemistryDOI: 10.1021/acs.jmedchem.7b00530
Source: Journal of Medicinal Chemistry - Category: Chemistry Authors: Source Type: research
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