Terry A. Panchal

发表

Evaluation of basic, heterocyclic ring systems as templates for use as potassium competitive acid blockers (pCABs).

E. Demont, A. Naylor, M. Bamford, 2009, Bioorganic & medicinal chemistry letters.

Novel Rho Kinase Inhibitors with Anti-inflammatory and Vasodilatory Activities

D. Behm, R. Bentley, C. Doe, 2007, Journal of Pharmacology and Experimental Therapeutics.

Design, Synthesis, and Biological Characterization of Inhaled p38α/β MAPK Inhibitors for the Treatment of Lung Inflammatory Diseases.

Valentina Bagnacani, Christopher A. Hurley, P. Puccini, 2022, Journal of medicinal chemistry.

Discovery of a brain-penetrant S1P₃-sparing direct agonist of the S1P₁ and S1P₅ receptors efficacious at low oral dose.

S. Dowell, K. Philpott, T. Heightman, 2011, Journal of medicinal chemistry.

A convenient synthesis of 4-(2-pyridyl)imidazolidine-2-thiones by the rearrangement of imidazo[1,5-a]pyridine-3-thione

Terry A. Panchal, D. Middlemiss, E. W. Collington, 1981 .

trans-2,5-Disubstituted pyrrolidines: Rapid stereocontrolled access from sulfones.

R. Pike, M. Moloney, Terry A. Panchal, 2006, Organic & biomolecular chemistry.

Discovery of a Selective S1P1 Receptor Agonist Efficacious at Low Oral Dose and Devoid of Effects on Heart Rate.

S. Dowell, E. Demont, J. Witherington, 2011, ACS medicinal chemistry letters.

(2R,5S)-2-Trichloromethyl-3-oxa-1-azabicyclo[3.3.0]octane-4,8-dione

R. Pike, M. Moloney, D. Watkin, 2005 .

The discovery of the benzazepine class of histamine H3 receptor antagonists.

Michael A. Briggs, Robert P. Davis, David M. Wilson, 2013, Bioorganic & medicinal chemistry letters.

Orally active C-6 heteroaryl- and heterocyclyl-substituted imidazo[1,2-a]pyridine acid pump antagonists (APAs).

E. Demont, A. Naylor, A. Takle, 2009, Bioorganic & medicinal chemistry letters.

Identification of clinical candidates from the benzazepine class of histamine H3 receptor antagonists.

David M. Wilson, A. Medhurst, P. Jeffrey, 2013, Bioorganic & medicinal chemistry letters.