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William J Greenlee

Showing results (1-10 of 90) with videos related to

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Protein Science : a Publication of the Protein Society|May 20, 2023
Exploring the inhibition of the soluble lytic transglycosylase Cj0843c of Campylobacter jejuni via targeting different sites with different scaffoldsVijay Kumar, Jacob Boorman, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|July 24, 2009
The discovery of azepane sulfonamides as potent 11beta-HSD1 inhibitorsSanthosh F Neelamkavil, Craig D Boyle, Samuel Chackalamannil, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Biaryl diamides as potent melanin concentrating hormone receptor 1 antagonistsAnandan Palani, Sherry Shapiro, Mark D McBriar, et al.
Bioorganic & Medicinal Chemistry|February 9, 2005
Discovery of melanin-concentrating hormone receptor R1 antagonists using high-throughput synthesisJing Su, Brian A McKittrick, Haiqun Tang, et al.
Bioorganic & Medicinal Chemistry Letters|April 13, 2007
Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 1Ginny D Ho, Ana Bercovici, Deen Tulshian, et al.
Bioorganic & Medicinal Chemistry Letters|January 13, 2010
Remote functionalization of SCH 39166: discovery of potent and selective benzazepine dopamine D1 receptor antagonistsT K Sasikumar, Duane A Burnett, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|March 18, 2004
Isopropyl amide derivatives of potent and selective muscarinic M2 receptor antagonistsAnandan Palani, Sundeep Dugar, John W Clader, et al.
Bioorganic & Medicinal Chemistry Letters|November 8, 2008
Structure-activity relationships of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of coughShu-Wei Yang, Ginny Ho, Deen Tulshian, et al.
Bioorganic & Medicinal Chemistry Letters|October 12, 2010
Design, synthesis, and structure-activity relationship studies of N-arylsulfonyl morpholines as γ-secretase inhibitorsHongmei Li, Ruo Xu, David Cole, et al.
Bioorganic & Medicinal Chemistry Letters|April 26, 2011
Synthesis and SAR study of tricyclic sulfones as γ-secretase inhibitors: C-6 and C-8 positionsJing Su, Haiqun Tang, Brian A McKittrick, et al.
Pageof 9

Showing results (1-10 of 90) with videos related to

Sort By:
Pageof 9
Protein Science : a Publication of the Protein Society|May 20, 2023
Exploring the inhibition of the soluble lytic transglycosylase Cj0843c of Campylobacter jejuni via targeting different sites with different scaffoldsVijay Kumar, Jacob Boorman, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|July 24, 2009
The discovery of azepane sulfonamides as potent 11beta-HSD1 inhibitorsSanthosh F Neelamkavil, Craig D Boyle, Samuel Chackalamannil, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2005
Biaryl diamides as potent melanin concentrating hormone receptor 1 antagonistsAnandan Palani, Sherry Shapiro, Mark D McBriar, et al.
Bioorganic & Medicinal Chemistry|February 9, 2005
Discovery of melanin-concentrating hormone receptor R1 antagonists using high-throughput synthesisJing Su, Brian A McKittrick, Haiqun Tang, et al.
Bioorganic & Medicinal Chemistry Letters|April 13, 2007
Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 1Ginny D Ho, Ana Bercovici, Deen Tulshian, et al.
Bioorganic & Medicinal Chemistry Letters|January 13, 2010
Remote functionalization of SCH 39166: discovery of potent and selective benzazepine dopamine D1 receptor antagonistsT K Sasikumar, Duane A Burnett, William J Greenlee, et al.
Bioorganic & Medicinal Chemistry Letters|March 18, 2004
Isopropyl amide derivatives of potent and selective muscarinic M2 receptor antagonistsAnandan Palani, Sundeep Dugar, John W Clader, et al.
Bioorganic & Medicinal Chemistry Letters|November 8, 2008
Structure-activity relationships of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of coughShu-Wei Yang, Ginny Ho, Deen Tulshian, et al.
Bioorganic & Medicinal Chemistry Letters|October 12, 2010
Design, synthesis, and structure-activity relationship studies of N-arylsulfonyl morpholines as γ-secretase inhibitorsHongmei Li, Ruo Xu, David Cole, et al.
Bioorganic & Medicinal Chemistry Letters|April 26, 2011
Synthesis and SAR study of tricyclic sulfones as γ-secretase inhibitors: C-6 and C-8 positionsJing Su, Haiqun Tang, Brian A McKittrick, et al.
Pageof 9