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American Chemical Society, Journal of Medicinal Chemistry, 4(60), p. 1534-1554, 2017

DOI: 10.1021/acs.jmedchem.6b01801

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Design and Elaboration of a Tractable Tricyclic Scaffold To Synthesize Druglike Inhibitors of Dipeptidyl Peptidase-4 (DPP-4), Antagonists of the C–C Chemokine Receptor Type 5 (CCR5), and Highly Potent and Selective Phosphoinositol-3 Kinase δ (PI3Kδ) Inhibitors

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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