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ACS.JMEDCHEM.7B00530
ACS.JMEDCHEM.7B00530
http://dx.doi.org/10.1021/ACS.JMEDCHEM.7B00530
Structure-Guided Synthesis and Mechanistic Studies Reveal Sweetspots on Naphthyl Salicyl Hydrazone Scaffold as Non-Nucleosidic Competitive, Reversible Inhibitors of Human Ribonucleotide Reductase.
P356
Q48099410-F53EB1D7-9333-44A2-BC42-9547679D6B0D
P356
ACS.JMEDCHEM.7B00530
http://dx.doi.org/10.1021/ACS.JMEDCHEM.7B00530