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Bioorganic & Medicinal Chemistry Letters|March 27, 2003
Novel and selective imidazole-containing biphenyl inhibitors of protein farnesyltransferaseMichael L Curtin, Alan S Florjancic, Jerome Cohen, et al.Bioorganic & Medicinal Chemistry Letters|February 15, 2008
Synthesis and in vitro activity of 1-(2,3-dichlorophenyl)-N-(pyridin-3-ylmethyl)-1H-1,2,4-triazol-5-amine and 4-(2,3-dichlorophenyl)-N-(pyridin-3-ylmethyl)-4H-1,2,4-triazol-3-amine P2X7 antagonistsAlan S Florjancic, Sridhar Peddi, Arturo Perez-Medrano, et al.Bioorganic & Medicinal Chemistry Letters|May 8, 2007
Novel and potent 3-(2,3-dichlorophenyl)-4-(benzyl)-4H-1,2,4-triazole P2X7 antagonistsWilliam A Carroll, Douglas M Kalvin, Arturo Perez Medrano, et al.Bioorganic & Medicinal Chemistry Letters|May 4, 2011
Synthesis and in vitro activity of N-benzyl-1-(2,3-dichlorophenyl)-1H-tetrazol-5-amine P2X(7) antagonistsArturo Perez-Medrano, Diana L Donnelly-Roberts, Alan S Florjancic, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Azaindole-Based Inhibitors of Cdc7 Kinase: Impact of the Pre-DFG Residue, Val 195Yunsong Tong, Kent D Stewart, Alan S Florjancic, et al.Bioorganic & Medicinal Chemistry Letters|February 14, 2012
Aminopyrimidinone cdc7 kinase inhibitorsKeith W Woods, Chunqiu Lai, Julie M Miyashiro, et al.Bioorganic & Medicinal Chemistry Letters|December 20, 2003
Structure-activity relationships of novel potent MurF inhibitorsYu Gui Gu, Alan S Florjancic, Richard F Clark, et al.ACS Medicinal Chemistry Letters|January 16, 2015
Pyrimidine-based tricyclic molecules as potent and orally efficacious inhibitors of wee1 kinaseYunsong Tong, Maricel Torrent, Alan S Florjancic, et al.The Journal of Organic Chemistry|November 1, 2023
Enabling, Decagram-Scale Synthesis of Macrocyclic MCL-1 Inhibitor ABBV-467Patrick B Brady, Bryan K Sorensen, Roberto M Risi, et al.Chemical Biology & Drug Design|February 24, 2006
Structure-based optimization of MurF inhibitorsGeoffrey F Stamper, Kenton L Longenecker, Elizabeth H Fry, et al.Pageof 2