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Bioorganic & Medicinal Chemistry Letters|October 4, 2007
3,5-Disubstituted quinolines as novel c-Jun N-terminal kinase inhibitorsRong Jiang, Derek Duckett, Weiming Chen, et al.Proceedings of the National Academy of Sciences of the United States of America|December 2, 2004
Structural basis for peptidoglycan binding by peptidoglycan recognition proteinsRongjin Guan, Abhijit Roychowdhury, Brian Ember, et al.Journal of Endotoxin Research|April 14, 2005
Crystal structure of a peptidoglycan recognition protein (PGRP) in complex with a muramyl tripeptide from Gram-positive bacteriaRongjin Guan, Abhijit Roychowdury, Brian Ember, et al.Bioorganic & Medicinal Chemistry Letters|March 21, 2007
Structure-activity relationships, and drug metabolism and pharmacokinetic properties for indazole piperazine and indazole piperidine inhibitors of ROCK-IIYangbo Feng, Michael D Cameron, Bozena Frackowiak, et al.The Journal of Biological Chemistry|September 1, 2005
Selective recognition of synthetic lysine and meso-diaminopimelic acid-type peptidoglycan fragments by human peptidoglycan recognition proteins I{alpha} and SSanjay Kumar, Abhijit Roychowdhury, Brian Ember, et al.Analytical Biochemistry|June 28, 2005
Time-resolved Forster resonance energy transfer assays for the binding of nucleotide and protein substrates to p38alpha protein kinaseWen Xiao Zhang, Ruixiu Wang, Douglas Wisniewski, et al.The Journal of Biological Chemistry|March 6, 2009
Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38Ted Kamenecka, Jeff Habel, Derek Duckett, et al.Journal of the American Chemical Society|June 19, 2008
Probing the substrate specificity of Golgi alpha-mannosidase II by use of synthetic oligosaccharides and a catalytic nucleophile mutantWei Zhong, Douglas A Kuntz, Brian Ember, et al.Bioorganic & Medicinal Chemistry Letters|May 13, 2009
Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitorsYouseung Shin, Weiming Chen, Jeff Habel, et al.Bioorganic & Medicinal Chemistry Letters|October 20, 2009
Benzothiazoles as Rho-associated kinase (ROCK-II) inhibitorsYan Yin, Li Lin, Claudia Ruiz, et al.Pageof 4