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Royal Society of Chemistry, Organic and Biomolecular Chemistry, 2(13), p. 549-560, 2015

DOI: 10.1039/c4ob01734j

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Synthesis and evaluation of protein arginine N-methyltransferase inhibitors designed to simultaneously occupy both substrate binding sites

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

PRMT inhibitors designed to simultaneously occupy both substrate binding sites display potent activity and surprising selectivity.