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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 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.Bioorganic & Medicinal Chemistry Letters|June 30, 2006
Modification of the clozapine structure by parallel synthesisJing Su, Haiqun Tang, Brian A McKittrick, et al.Journal of the American Chemical Society|May 16, 2018
Chemoselective Peptide Modification via Photocatalytic Tryptophan β-Position ConjugationYounong Yu, Li-Kang Zhang, Alexei V Buevich, et al.Bioorganic & Medicinal Chemistry|June 19, 2007
SAR study of bicyclo[4.1.0]heptanes as melanin-concentrating hormone receptor R1 antagonists: taming hERGJing Su, Brian A McKittrick, Haiqun Tang, et al.Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Discovery of new SCH 39166 analogs as potent and selective dopamine D1 receptor antagonistsLi Qiang, T K Sasikumar, Duane A Burnett, et al.Bioorganic & Medicinal Chemistry Letters|July 3, 2007
Synthesis of novel bicyclo[4.1.0]heptane and bicyclo[3.1.0]hexane derivatives as melanin-concentrating hormone receptor R1 antagonistsJing Su, Haiqun Tang, Brian A McKittrick, 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.Bioorganic & Medicinal Chemistry Letters|February 22, 2014
Quality by design (QbD) of amide isosteres: 5,5-Disubstituted isoxazolines as potent CRTh2 antagonists with favorable pharmacokinetic and drug-like propertiesDong Xiao, Xiaohong Zhu, Younong Yu, et al.Bioorganic & Medicinal Chemistry Letters|March 19, 2010
Design and synthesis of tricyclic sulfones as gamma-secretase inhibitors with greatly reduced Notch toxicityRuo Xu, David Cole, Ted Asberom, et al.Pageof 2