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Journal of Biomolecular Screening|March 31, 2012
In vitro ADME profiling using high-throughput rapidfire mass spectrometry: cytochrome p450 inhibition and metabolic stability assaysXiang Wu, Jing Wang, Lory Tan, et al.Protein Expression and Purification|July 4, 2006
Expression and characterization of recombinant gamma-tryptaseJing Yuan, Jeri Beltman, Erik Gjerstad, et al.Journal of Medicinal Chemistry|May 12, 2006
Optimization of subsite binding to the beta5 subunit of the human 20S proteasome using vinyl sulfones and 2-keto-1,3,4-oxadiazoles: syntheses and cellular properties of potent, selective proteasome inhibitorsRobert M Rydzewski, Leland Burrill, Rohan Mendonca, et al.Bioorganic & Medicinal Chemistry Letters|February 4, 2006
Factor VIIa inhibitors: improved pharmacokinetic parametersAleksandr Kolesnikov, Roopa Rai, Wendy B Young, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2006
Potent 4-amino-5-azaindole factor VIIa inhibitorsHuiyong Hu, Aleksandr Kolesnikov, Jennifer R Riggs, et al.Journal of Molecular Biology|November 4, 2004
Dissecting and designing inhibitor selectivity determinants at the S1 site using an artificial Ala190 protease (Ala190 uPA)Bradley A Katz, Christine Luong, Joseph D Ho, et al.Biochemistry|May 10, 2006
Structure-guided design of peptide-based tryptase inhibitorsMary E McGrath, Paul A Sprengeler, Bernard Hirschbein, et al.Pageof 1