M. Wennerholm

发表

Preclinical Characterization of the FAAH Inhibitor JNJ-42165279.

Sandy J. Wilson, M. Karbarz, S. Chaplan, 2015, ACS medicinal chemistry letters.

The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors.

Sandy J. Wilson, M. Karbarz, S. Chaplan, 2016, Bioorganic & medicinal chemistry letters.

Identification and SAR of Glycine Benzamides as Potent Agonists for the GPR139 Receptor.

P. Bonaventure, C. Dvorak, T. Lovenberg, 2015, ACS medicinal chemistry letters.

Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate.

Sandy J. Wilson, M. Karbarz, S. Chaplan, 2012, ACS medicinal chemistry letters.

Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase

Sandy J. Wilson, Jiejun Wu, M. Karbarz, 2009, Anesthesia and analgesia.

Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase.

Sandy J. Wilson, Jiejun Wu, K. Pattabiraman, 2008, Bioorganic & medicinal chemistry letters.

1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase.

Sandy J. Wilson, M. Karbarz, S. Chaplan, 2014, Bioorganic & medicinal chemistry letters.

Pharmacologic Characterization of JNJ-42226314, [1-(4-Fluorophenyl)indol-5-yl]-[3-[4-(thiazole-2-carbonyl)piperazin-1-yl]azetidin-1-yl]methanone, a Reversible, Selective, and Potent Monoacylglycerol Lipase Inhibitor

P. Bonaventure, T. Lovenberg, P. Connolly, 2019, The Journal of Pharmacology and Experimental Therapeutics.

A Selective Orexin-1 Receptor Antagonist Attenuates Stress-Induced Hyperarousal without Hypnotic Effects

T. P. Lebold, P. Bonaventure, T. Lovenberg, 2015, The Journal of Pharmacology and Experimental Therapeutics.

Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase.

M. Karbarz, S. Chaplan, J. Keith, 2014, Bioorganic & medicinal chemistry letters.

Heteroarylureas with Fused Bicyclic Diamine Cores as Inhibitors of Fatty Acid Amide Hydrolase.

M. Karbarz, S. Chaplan, J. Keith, 2020, Bioorganic & medicinal chemistry letters.

Evaluation of JNJ-54717793 a Novel Brain Penetrant Selective Orexin 1 Receptor Antagonist in Two Rat Models of Panic Attack Provocation

P. Bonaventure, T. Lovenberg, A. Shekhar, 2017, Front. Pharmacol..

Selective Inhibition of Orexin-2 Receptors Prevents Stress-Induced ACTH Release in Mice

P. Bonaventure, T. Lovenberg, C. Dugovic, 2017, Frontiers in Behavioral Neuroscience.

Ablation of primary afferent terminals reduces nicotinic receptor expression and the nociceptive responses to nicotinic agonists in the spinal cord

T. Deerinck, P. Taylor, T. Yaksh, 2004, Journal of neurocytology.