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Ruth E. Tenbrink

Upjohn

31

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Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases.

2018 Journal of Medicinal Chemistry
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Pyrrolo [2,3-d] pyrimidine as inhibitors of Janus kinases (JAK)

2014
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Differential pharmacology between the guinea-pig and the gorilla 5-HT1D receptor as probed with isochromans (5-HT1D-selective ligands).

1999 British Journal of Pharmacology
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Pharmacological characterization of U-101387, a dopamine D4 receptor selective antagonist.

1996 Journal of Pharmacology and Experimental Therapeutics
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A model for the dopamine D4 pharmacophore

1996 Acta Crystallographica Section A
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(S)-(−)-4-[4-[2-(Isochroman-1-yl)ethyl]piperazin-1-yl]benzenesulfonamide, a Selective Dopamine D4 Antagonist

1996 Journal of Medicinal Chemistry
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High-Affinity Partial Agonist Imidazo[1,5-a]quinoxaline Amides, Carbamates, and Ureas at the γ-Aminobutyric Acid A/Benzodiazepine Receptor Complex†

1996 Journal of Medicinal Chemistry
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Chapter 5. Recent Advances in Dopamine D3 and D4 Receptor Ligands and Pharmacology

1994 Annual Reports in Medicinal Chemistry
- Ruth E. Tenbrink
- Rita M. Huff
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Antagonist, partial agonist, and full agonist imidazo[1,5-a]quinoxaline amides and carbamates acting through the GABAA/benzodiazepine receptor.

1994 Journal of Medicinal Chemistry
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Inhibitors of the protease from human immunodeficiency virus : synthesis, enzyme inhibition, and antiviral activity of a series of compounds containing the dihydroxyethylene transition-state isostere

1993 Journal of Medicinal Chemistry
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Citations (24)