Huong T. Dang

3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109b.

D. Connolly, S. Tamura, C. Sage, 2007, Bioorganic & medicinal chemistry letters.

Fluorinated pyrazole acids are agonists of the high affinity niacin receptor GPR109a.

D. Connolly, S. Tamura, Vu P Hong, 2007, Bioorganic & medicinal chemistry letters.

Discovery of a lead series of potent benzodiazepine 5-HT2C receptor agonists with high selectivity in functional and binding assays.

C. Sage, Albert S. Ren, Michael E. Morgan, 2019, Bioorganic & medicinal chemistry letters.

Novel (R)-6,6a,7,8,9,10-hexahydro-5H-pyrazino[1,2-a][1,n]naphthyridines as potent and selective agonists of the 5-HT2C receptor.

Albert S. Ren, K. Whelan, A. Grottick, 2021, Bioorganic & medicinal chemistry letters.

Tetrahydroquinoline-based tricyclic amines as potent and selective agonists of the 5-HT2C receptor.

C. Sage, Albert S. Ren, K. Whelan, 2016, Bioorganic & medicinal chemistry letters.

Discovery of 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalen-4-carboxamides as potent and selective CB2 receptor agonists.

I. Gaidarov, Michael E. Morgan, K. Whelan, 2015, Bioorganic & medicinal chemistry letters.

Inhibition of Mas G-protein signaling improves coronary blood flow, reduces myocardial infarct size, and provides long-term cardioprotection.

John W. Adams, D. Connolly, Zhuangjie Li, 2012, American journal of physiology. Heart and circulatory physiology.

Kinetics of 5-HT2B Receptor Signaling: Profound Agonist-Dependent Effects on Signaling Onset and Duration

I. Gaidarov, John M Frazer, D. Unett, 2013, The Journal of Pharmacology and Experimental Therapeutics.