K. Sullivan

发表

Induction of Ca2+-Activated K+ Current and Transient Outward Currents in Human Capillary Endothelial Cells

R. Numann, F. Jow, R. Numann, 1999, The Journal of Membrane Biology.

Synthesis and biological evaluation of novel compounds within a class of 3-aminochroman derivatives with dual 5-HT1A receptor and serotonin transporter affinity.

B. Harrison, D. Huryn, C. Beyer, 2006, Journal of medicinal chemistry.

Studies toward the discovery of the next generation of antidepressants. Part 5: 3,4-Dihydro-2H-benzo[1,4]oxazine derivatives with dual 5-HT1A receptor and serotonin transporter affinity.

B. Harrison, L. Schechter, D. Smith, 2006, Bioorganic & medicinal chemistry letters.

Studies towards the next generation of antidepressants. Part 4: derivatives of 4-(5-fluoro-1H-indol-3-yl)cyclohexylamine with affinity for the serotonin transporter and the 5-HT1A receptor.

Richard E Mewshaw, L. Schechter, D. Smith, 2005, Bioorganic & medicinal chemistry letters.

The synthesis and biological evaluation of quinolyl-piperazinyl piperidines as potent serotonin 5-HT1A antagonists.

M. Day, T. Comery, S. Grauer, 2010, Journal of medicinal chemistry.

Advances toward new antidepressants with dual serotonin transporter and 5-HT1A receptor affinity within a class of 3-aminochroman derivatives. Part 2.

B. Harrison, Minsheng Zhang, A. Failli, 2008, Journal of medicinal chemistry.

Tetrahydrocarbazole-based serotonin reuptake inhibitor/dopamine D2 partial agonists for the potential treatment of schizophrenia.

K. Marquis, S. Grauer, J. Brennan, 2009, Bioorganic & medicinal chemistry letters.

Correlating Efficacy in Rodent Cognition Models with In Vivo 5-HT 1 A Receptor Occupancy by a Novel Antagonist

Hughes, M. Day, T. Comery, 2008 .

Correlating Efficacy in Rodent Cognition Models with in Vivo 5-Hydroxytryptamine1A Receptor Occupancy by a Novel Antagonist, (R)-N-(2-Methyl-(4-indolyl-1-piperazinyl)ethyl)-N-(2-pyridinyl)-cyclohexane Carboxamide (WAY-101405)

M. Day, T. Comery, S. Grauer, 2008, Journal of Pharmacology and Experimental Therapeutics.

Pituitary adenylate cyclase-activating peptide (PACAP) induces differentiation in the neuronal F11 cell line through a PKA-dependent pathway

A. Baudy, J. Dunlop, M. Fennell, 2006, Brain Research.

Aplindore (DAB-452), a high affinity selective dopamine D2 receptor partial agonist.

K. Marquis, J. Brennan, G. Stack, 2006, European Journal of Pharmacology.

Synthesis and structure-activity relationship of novel lactam-fused chroman derivatives having dual affinity at the 5-HT(1A) receptor and the serotonin transporter.

B. Harrison, W. Childers, Zhongqi Shen, 2010, Bioorganic & medicinal chemistry letters.

The identification of neurotensin NTS1 receptor partial agonists through a ligand-based virtual screening approach.

M. Pausch, M. Popiolek, Yi-Ran Fan, 2008, Bioorganic & medicinal chemistry letters.