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Joseph Dudash

Johnson & Johnson Pharmaceutical Research and Development

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Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors.

2005 Bioorganic & Medicinal Chemistry Letters
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Glycosylated dihydrochalcones as potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitors

2004 Bioorganic & Medicinal Chemistry Letters
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Benzoxazinones as PPARgamma agonists. 2. SAR of the amide substituent and in vivo results in a type 2 diabetes model.

2004 Journal of Medicinal Chemistry
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Derives de (3-oxo-3, 4-dihydro-quinoxalin-2-yl-amino)-benzamide et composes afferents comme inhibiteurs de la glycogene phosphorylase dans le traitement du diabete et de l'obesite

2004
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