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Anandan Palani

Showing results (31-40 of 56) with videos related to

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Journal of Medicinal Chemistry|August 14, 2020
Generation of Leads for γ-Secretase ModulationMihirbaran Mandal, Alexei Buevich, John P Caldwell, et al.
Bioorganic & Medicinal Chemistry Letters|January 4, 2011
Discovery of fused 5,6-bicyclic heterocycles as γ-secretase modulatorsJun Qin, Pawan Dhondi, Xianhai Huang, et al.
Journal of Medicinal Chemistry|July 22, 2005
Biaryl ureas as potent and orally efficacious melanin concentrating hormone receptor 1 antagonists for the treatment of obesityAnandan Palani, Sherry Shapiro, Mark D McBriar, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2003
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. III: synthesis, antiviral and pharmacokinetic profiles of symmetrical heteroaryl carboxamidesStuart W McCombie, Jayaram R Tagat, Susan F Vice, et al.
Virology|February 24, 2006
Interaction of small molecule inhibitors of HIV-1 entry with CCR5Christoph Seibert, Weiwen Ying, Svetlana Gavrilov, et al.
Bioorganic & Medicinal Chemistry|January 31, 2006
Bicyclic[4.1.0]heptanes as phenyl replacements for melanin concentrating hormone receptor antagonistsRuo Xu, Shengjian Li, Jaroslava Paruchova, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2012
SAR studies of C2 ethers of 2H-pyrano[2,3-d]pyrimidine-2,4,7(1H,3H)-triones as nicotinic acid receptor (NAR) agonistXianhai Huang, Jing Su, Ashwin U Rao, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a potent thiadiazole class of histamine h3 receptor antagonist for the treatment of diabetesAshwin U Rao, Ning Shao, Robert G Aslanian, et al.
Chemmedchem|July 26, 2017
Development of a New Structural Class of Broadly Acting HCV Non-Nucleoside Inhibitors Leading to the Discovery of MK-8876Casey C McComas, Anandan Palani, Wei Chang, et al.
Journal of Medicinal Chemistry|March 31, 2006
Discovery of orally efficacious melanin-concentrating hormone receptor-1 antagonists as antiobesity agents. Synthesis, SAR, and biological evaluation of bicyclo[3.1.0]hexyl ureasMark D McBriar, Henry Guzik, Sherry Shapiro, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|August 14, 2020
Generation of Leads for γ-Secretase ModulationMihirbaran Mandal, Alexei Buevich, John P Caldwell, et al.
Bioorganic & Medicinal Chemistry Letters|January 4, 2011
Discovery of fused 5,6-bicyclic heterocycles as γ-secretase modulatorsJun Qin, Pawan Dhondi, Xianhai Huang, et al.
Journal of Medicinal Chemistry|July 22, 2005
Biaryl ureas as potent and orally efficacious melanin concentrating hormone receptor 1 antagonists for the treatment of obesityAnandan Palani, Sherry Shapiro, Mark D McBriar, et al.
Bioorganic & Medicinal Chemistry Letters|February 5, 2003
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. III: synthesis, antiviral and pharmacokinetic profiles of symmetrical heteroaryl carboxamidesStuart W McCombie, Jayaram R Tagat, Susan F Vice, et al.
Virology|February 24, 2006
Interaction of small molecule inhibitors of HIV-1 entry with CCR5Christoph Seibert, Weiwen Ying, Svetlana Gavrilov, et al.
Bioorganic & Medicinal Chemistry|January 31, 2006
Bicyclic[4.1.0]heptanes as phenyl replacements for melanin concentrating hormone receptor antagonistsRuo Xu, Shengjian Li, Jaroslava Paruchova, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2012
SAR studies of C2 ethers of 2H-pyrano[2,3-d]pyrimidine-2,4,7(1H,3H)-triones as nicotinic acid receptor (NAR) agonistXianhai Huang, Jing Su, Ashwin U Rao, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a potent thiadiazole class of histamine h3 receptor antagonist for the treatment of diabetesAshwin U Rao, Ning Shao, Robert G Aslanian, et al.
Chemmedchem|July 26, 2017
Development of a New Structural Class of Broadly Acting HCV Non-Nucleoside Inhibitors Leading to the Discovery of MK-8876Casey C McComas, Anandan Palani, Wei Chang, et al.
Journal of Medicinal Chemistry|March 31, 2006
Discovery of orally efficacious melanin-concentrating hormone receptor-1 antagonists as antiobesity agents. Synthesis, SAR, and biological evaluation of bicyclo[3.1.0]hexyl ureasMark D McBriar, Henry Guzik, Sherry Shapiro, et al.
Pageof 6