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ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a potent nicotinic Acid receptor agonist for the treatment of dyslipidemiaJun Qin, Ashwin Rao, Xiao Chen, et al.Bioorganic & Medicinal Chemistry Letters|June 19, 2008
Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonistsUnmesh Shah, Claire M Lankin, Craig D Boyle, et al.ACS Medicinal Chemistry Letters|July 14, 2026
Discovery of Biased Dual-Agonists of Glucagon-Like Peptide 1 and Glucagon Receptors through Mutation of a Conserved AspartateRobert E Thompson, Aditya J Desai, Dmitri Pissarnitski, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Synthesis and SAR Studies of Fused Oxadiazines as γ-Secretase Modulators for Treatment of Alzheimer's DiseaseXianhai Huang, Wei Zhou, Xiaoxiang Liu, et al.Bioorganic & Medicinal Chemistry Letters|February 26, 2004
SAR development of polycyclic guanine derivatives targeted to the discovery of a selective PDE5 inhibitor for treatment of erectile dysfunctionDmitri A Pissarnitski, Theodros Asberom, Craig D Boyle, et al.ACS Medicinal Chemistry Letters|November 19, 2021
Comprehensive Strategies to Bicyclic Prolines: Applications in the Synthesis of Potent Arginase InhibitorsDerun Li, Hongjun Zhang, Thomas W Lyons, et al.ACS Medicinal Chemistry Letters|September 16, 2021
Structure-Based Discovery of Proline-Derived Arginase Inhibitors with Improved Oral Bioavailability for Immuno-OncologyMin Lu, Hongjun Zhang, Derun Li, et al.ACS Medicinal Chemistry Letters|April 16, 2020
Discovery and Optimization of Rationally Designed Bicyclic Inhibitors of Human Arginase to Enhance Cancer ImmunotherapyMatthew J Mitcheltree, Derun Li, Abdelghani Achab, et al.Journal of Medicinal Chemistry|December 3, 2002
Improving the oral efficacy of CNS drug candidates: discovery of highly orally efficacious piperidinyl piperidine M2 muscarinic receptor antagonistsYuguang Wang, Samuel Chackalamannil, Zhiyong Hu, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2002
Design and synthesis of xanthine analogues as potent and selective PDE5 inhibitorsYuguang Wang, Samuel Chackalamannil, Zhiyong Hu, et al.Pageof 7