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Jun Z. Xu

Johnson & Johnson Pharmaceutical Research and Development

12

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524

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Synthesis and Biological Evaluation of 3-Aryl-3-(4-phenoxy)-propionic Acid as a Novel Series of G Protein-Coupled Receptor 40 Agonists

2007 Journal of Medicinal Chemistry
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Synthesis and Identification of [1,2,4]Thiadiazole Derivatives as a New Series of Potent and Orally Active Dual Agonists of Peroxisome Proliferator-Activated Receptors α and δ

2007 Journal of Medicinal Chemistry
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Pharmacological profile of a novel, non‐TZD PPARγ agonist

2005 Diabetes, Obesity and Metabolism
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Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3β (GSK-3β) inhibitors

2004 Bioorganic & Medicinal Chemistry
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3-(7-Azaindolyl)-4-arylmaleimides as potent, selective inhibitors of glycogen synthase kinase-3

2004 Bioorganic & Medicinal Chemistry Letters
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Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors☆

2004 Bioorganic & Medicinal Chemistry
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Synthesis and Discovery of Macrocyclic Polyoxygenated Bis-7-azaindolylmaleimides as a Novel Series of Potent and Highly Selective Glycogen Synthase Kinase-3β Inhibitors

2003 Journal of Medicinal Chemistry
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Macrocyclic bisindolylmaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3

2003 Bioorganic & Medicinal Chemistry Letters
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Benzoxazinones as PPARγ agonists. part 1: SAR of three aromatic regions

2003 Bioorganic & Medicinal Chemistry Letters
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Human TE671 cells express functional motilin receptors

2001 Biotechnology Letters
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