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Discovery of GSK3527497: A Candidate for the Inhibition of Transient Receptor Potential Vanilloid‑4 (TRPV4)

Journal of medicinal chemistry, 2019-10, Vol.62 (20), p.9270-9280

2019

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Evaluation of Potent and Selective Small-Molecule Antagonists for the CXCR2 Chemokine Receptor

Journal of medicinal chemistry, 2004-03, Vol.47 (6), p.1319-1321

2004

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Comparison of N, N′-diarylsquaramides and N, N′-diarylureas as antagonists of the CXCR2 chemokine receptor

Bioorganic & medicinal chemistry letters, 2007-03, Vol.17 (6), p.1713-1717

2007

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Discovery of potent and orally bioavailable N, N′-diarylurea antagonists for the CXCR2 chemokine receptor

Bioorganic & medicinal chemistry letters, 2004-09, Vol.14 (17), p.4375-4378

2004

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Mechanistic Studies of the Zirconium−Triisopropanolamine-Catalyzed Enantioselective Addition of Azide to Cyclohexene Oxide

Journal of organic chemistry, 1998-09, Vol.63 (19), p.6656-6666

1998

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Homogeneous catalysis as a tool for organic synthesis

Pure and applied chemistry, 1998-01, Vol.70 (5), p.1041-1046

1998

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Discovery of GSK3527497: A Candidate for the Inhibition of Transient Receptor Potential Vanilloid‑4 (TRPV4)

Evaluation of Potent and Selective Small-Molecule Antagonists for the CXCR2 Chemokine Receptor

Design and Optimization of Sulfone Pyrrolidine Sulfonamide Antagonists of Transient Receptor Potential Vanilloid‑4 with in Vivo Activity in a Pulmonary Edema Model

Comparison of N, N′-diarylsquaramides and N, N′-diarylureas as antagonists of the CXCR2 chemokine receptor

Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered through X‑ray Fragment Screening

Discovery of potent and orally bioavailable N, N′-diarylurea antagonists for the CXCR2 chemokine receptor

Mechanistic Studies of the Zirconium−Triisopropanolamine-Catalyzed Enantioselective Addition of Azide to Cyclohexene Oxide

Homogeneous catalysis as a tool for organic synthesis

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