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Magda F. Morton

Johnson & Johnson Pharmaceutical Research and Development

22

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JNJ-26070109 [( R )4-Bromo- N -[1-(2,4-difluoro-phenyl)-ethyl]-2-(quinoxaline-5-sulfonylamino)-benzamide]: A Novel, Potent, and Selective Cholecystokinin 2 Receptor Antagonist with Good Oral Bioavailability

2011 Journal of Pharmacology and Experimental Therapeutics
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Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists I: Discovery of CCKR1 selectivity in a previously CCKR2-selective lead series

2009 Bioorganic & Medicinal Chemistry Letters
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Characterization of a Robust Enzymatic Assay for Inhibitors of 2-Oxoglutarate-Dependent Hydroxylases

2009 Journal of Biomolecular Screening
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Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists II: tuning of receptor selectivity and in vivo efficacy.

2009 Bioorganic & Medicinal Chemistry Letters
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Retracted notice to: Obestatin reduces food intake and suppresses body weight gain in rodents [Biochem. Biophys. Res. Commun. 357(1) (2007) 264-269]

2009 Biochemical and Biophysical Research Communications
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Discovery of potent cholecystokinin-2 receptor antagonists: elucidation of key pharmacophore elements by X-ray crystallographic and NMR conformational analysis.

2008 Bioorganic & Medicinal Chemistry
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Peripheral administration of obestatin reduces food intake and suppresses body weight gain in lean mice and rats

2007 The FASEB Journal
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SAR studies of 1,5-diarylpyrazole-based CCK1 receptor antagonists

2007 Bioorganic & Medicinal Chemistry Letters
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RETRACTED: Obestatin reduces food intake and suppresses body weight gain in rodents

2007 Biochemical and Biophysical Research Communications
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Identification and Optimization of Anthranilic Sulfonamides as Novel, Selective Cholecystokinin-2 Receptor Antagonists

2006 Journal of Medicinal Chemistry
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Citations (35)