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Journal of Medicinal Chemistry|September 10, 1999
Design, synthesis, and evaluation of chromen-2-ones as potent and selective human dopamine D4 antagonistsS R Kesten, T G Heffner, S J Johnson, et al.Journal of Medicinal Chemistry|December 25, 1992
2-(aminoalkyl)-5-nitropyrazolo[3,4,5-kl]acridines, a new class of anticancer agentsD B Capps, J Dunbar, S R Kesten, et al.Catheterization and Cardiovascular Diagnosis|February 1, 1997
Percutaneous method of laser transmyocardial revascularizationC B Kim, R Kesten, M Javier, et al.Bioorganic & Medicinal Chemistry Letters|February 26, 2004
Subtype selective NMDA receptor antagonists: evaluation of some novel alkynyl analoguesBrian E Kornberg, Sham S Nikam, Jon L Wright, et al.Journal of Medicinal Chemistry|October 14, 1994
The discovery and structure-activity relationships of 1,2,3,6-tetrahydro-4-phenyl-1-[(arylcyclohexenyl)alkyl]pyridines. Dopamine autoreceptor agonists and potential antipsychotic agentsJ L Wright, B W Caprathe, D M Downing, et al.Journal of Medicinal Chemistry|September 9, 2000
Subtype-selective N-methyl-D-aspartate receptor antagonists: synthesis and biological evaluation of 1-(heteroarylalkynyl)-4-benzylpiperidinesJ L Wright, T F Gregory, S R Kesten, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Isoindolinone enantiomers having affinity for the dopamine D4 receptorT R Belliotti, W A Brink, S R Kesten, et al.Journal of Medicinal Chemistry|March 26, 1998
Aminopyrimidines with high affinity for both serotonin and dopamine receptorsD Wustrow, T Belliotti, S Glase, et al.Journal of Medicinal Chemistry|March 15, 2000
Synthesis of N-substituted 4-(4-hydroxyphenyl)piperidines, 4-(4-hydroxybenzyl)piperidines, and (+/-)-3-(4-hydroxyphenyl)pyrrolidines: selective antagonists at the 1A/2B NMDA receptor subtypeA P Guzikowski, A P Tamiz, M Acosta-Burruel, et al.ACS Medicinal Chemistry Letters|June 14, 2011
Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH InhibitorDouglas S Johnson, Cory Stiff, Scott E Lazerwith, et al.Pageof 2