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Bioorganic & Medicinal Chemistry Letters|February 17, 2020
Multi-step parallel synthesis enabled optimization of benzofuran derivatives as pan-genotypic non-nucleoside inhibitors of HCV NS5BDong Xiao, Xing Dai, Hong Liu, et al.Bioorganic & Medicinal Chemistry Letters|March 18, 2003
Oximino-piperidino-piperidine-based CCR5 antagonists. Part 2: synthesis, SAR and biological evaluation of symmetrical heteroaryl carboxamidesAnandan Palani, Sherry Shapiro, John W Clader, et al.Bioorganic & Medicinal Chemistry Letters|December 21, 2011
Facile synthesis of tetracyclic azepine and oxazocine derivatives and their potential as MAPKAP-K2 (MK2) inhibitorsAshwin U Rao, Dong Xiao, Xianhai Huang, et al.Bioorganic & Medicinal Chemistry Letters|February 14, 2012
Synthesis and structure-activity relationship (SAR) study of 4-azabenzoxazole analogues as H3 antagonistsNing Shao, Robert Aslanian, Robert E West, 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.ACS Medicinal Chemistry Letters|August 18, 2022
Discovery of Insulin/GLP-1/Glucagon Triagonists for the Treatment of Diabetes and ObesityChunhui Huang, Anandan Palani, Zhiqiang Yang, et al.Bioorganic & Medicinal Chemistry Letters|November 4, 2018
Design and evaluation of novel tetracyclic benzofurans as palm site allosteric inhibitors of HCV NS5B polymeraseHong Liu, Xing Dai, Shuwen He, et al.Bioorganic & Medicinal Chemistry Letters|December 31, 2008
Spiro-piperidine azetidinones as potent TRPV1 antagonistsDong Xiao, Anandan Palani, Robert Aslanian, 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|December 16, 2011
A three-step protocol for lead optimization: quick identification of key conformational features and functional groups in the SAR studies of non-ATP competitive MK2 (MAPKAPK2) inhibitorsXianhai Huang, Xiaohong Zhu, Xiao Chen, et al.Pageof 7