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Journal of Medicinal Chemistry|February 4, 2005
Dopamine D1/D5 receptor antagonists with improved pharmacokinetics: design, synthesis, and biological evaluation of phenol bioisosteric analogues of benzazepine D1/D5 antagonistsWen-Lian Wu, Duane A Burnett, Richard Spring, et al.Journal of Medicinal Chemistry|August 1, 1989
(3-Amino-2-oxoalkyl)phosphonic acids and their analogues as novel inhibitors of D-alanine:D-alanine ligaseP K Chakravarty, W J Greenlee, W H Parsons, et al.Plos One|May 2, 2018
Is a clean river fun for all? Recognizing social vulnerability in watershed planningBethany B Cutts, Andrew J Greenlee, Natalie K Prochaska, et al.Journal of Virology|July 14, 2017
Experimental Transmission of the Chronic Wasting Disease Agent to Swine after Oral or Intracranial InoculationS Jo Moore, M Heather West Greenlee, Naveen Kondru, et al.Bioorganic & Medicinal Chemistry Letters|April 11, 2007
Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 2Ginny D Ho, Ana Bercovici, Deen Tulshian, et al.Journal of Medicinal Chemistry|August 15, 2009
Discovery of orally active 3-pyridinyl-tropane as a potent nociceptin receptor agonist for the management of coughShu-Wei Yang, Ginny Ho, Deen Tulshian, et al.Journal of Medicinal Chemistry|June 28, 2002
Synthesis, SAR, and biological evaluation of oximino-piperidino-piperidine amides. 1. Orally bioavailable CCR5 receptor antagonists with potent anti-HIV activityAnandan Palani, Sherry Shapiro, Hubert Josien, et al.The Journal of Experimental Biology|August 29, 2024
HIF signaling in the prothoracic gland regulates growth and development in hypoxia but not normoxia in DrosophilaJacob B Campbell, Alexander W Shingleton, Kendra J Greenlee, et al.Bioorganic & Medicinal Chemistry Letters|May 25, 2010
Tricyclic sulfones as orally active gamma-secretase inhibitors: synthesis and structure-activity relationship studiesT K Sasikumar, Li Qiang, Duane A Burnett, et al.Journal of Medicinal Chemistry|October 13, 2007
Discovery of orally efficacious tetracyclic metabotropic glutamate receptor 1 (mGluR1) antagonists for the treatment of chronic painWen-Lian Wu, Duane A Burnett, Martin Domalski, et al.Pageof 30