Biotransformation of the Antiviral Drugs Acyclovir and Penciclovir in Activated Sludge Treatment | Environmental Science & Technology
Ozonation of Propranolol: Formation of Oxidation Products | Environmental Science & Technology
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Discovery of the Potent and Selective MC4R Antagonist PF-07258669 for the Potential Treatment of Appetite Loss | Journal of Medicinal Chemistry
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Discovery of the Potent and Selective MC4R Antagonist PF-07258669 for the Potential Treatment of Appetite Loss | Journal of Medicinal Chemistry
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Hospital Wastewater Treatment by Membrane Bioreactor: Performance and Efficiency for Organic Micropollutant Elimination | Environmental Science & Technology
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Strategies to Reduce Low-Value Cardiovascular Care: A Scientific Statement From the American Heart Association | Circulation: Cardiovascular Quality and Outcomes
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Discovery of the Potent and Selective MC4R Antagonist PF-07258669 for the Potential Treatment of Appetite Loss | Journal of Medicinal Chemistry
![Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based ...](https://pubs.acs.org/cms/10.1021/acs.jmedchem.7b00231/asset/images/medium/jm-2017-002314_0018.gif "Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based ...")
Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based ...
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Metabolism-Directed Design of Oxetane-Containing Arylsulfonamide Derivatives as γ-Secretase Inhibitors | Journal of Medicinal Chemistry
Metabolism-Directed Design of Oxetane-Containing Arylsulfonamide Derivatives as γ-Secretase Inhibitors | Journal of Medicinal Chemistry
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Strategies to Reduce Low-Value Cardiovascular Care: A Scientific Statement From the American Heart Association | Circulation: Cardiovascular Quality and Outcomes
Design and Synthesis of Functionally Active 5-Amino-6-Aryl Pyrrolopyrimidine Inhibitors of Hematopoietic Progenitor Kinase 1 | Journal of Medicinal Chemistry
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![Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/jm300094u/asset/images/jm300094u.social.jpeg_v03 "Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor | Journal of Medicinal Chemistry")
Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor | Journal of Medicinal Chemistry
