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Baldwin, P.; Reeves, A.; Powell, K.; Napier, R.; Swimm, A.; Sun, A.; Giesler, K.; Bommarius, B.; Shinnick, T.; Snyder, J.; Liotta, D.; Kalman, D. Monocarbonyl analogs of curcumin inhibit growth of antibiotic sensitive and resistant strains of Mycobacterium tuberculosis. Eur. J. of Med. Chem., 2015, 92: 693-699.
Khatri, A.; Burger, P.; Swanger, S.; Hansen, K.; Zimmerman, S.; Karakas, E.; Liotta, D.; Furukawa, H.; Snyder, J.; Traynelis, S. Structural Determinants and Mechanism of Action of GluN2C-selective NMDA Receptor Positive Allosteric Modulator. Mol. Pharmacol., 2014, 86:548–560.
Zhu, S.; Kisiel, W.; Lu, Y.; Petersen, L.; Ndungu, J.; Moore, T.; Parker, E.; Sun, A.; Liotta, D.; El-Rayes, B.; Brat, D.; Snyder, J.; Shoji, M. Tumor Angieogenesis Therapy Using Targeted Delivery of Pacclitaxel to the Vasculature of Breast Cancer Metastases. J. Drug Deliv., 2014
Zhu, S.; Kisiel, W.; Lu, Y.; Petersen, L.; Ndungu, J.; Moore, T.; Parker, E.; Sun, A.; Sarkaria, J.; Snyder, J.; Liotta, D.; Brat, D.; El-Rayes, B.; Shoji, M. Visualizing cancer and response to therapy in vivo using Cy5.5-labeled factor VIIa and anti-tissue factor antibody. J. Drug Target. 2014, 16:1-9.
Strong, K.; Jing, Y.; Prosser, A.; Traynelis, S.; Liotta, D. NMDA receptor modulators: an updated patent review (2013-2014). Expert Opin. Ther. Patents., 2014, 24(12), 1349-1366.
Zhou, T.; Ye, L.; Bai, Y.; Sun, A.; Cox, B.; Liu, D.; Li, Y.; Liotta, D.; Snyder, J.; Fu, H. Autophagy and apoptosis in hepatocellular carcinoma induced by EF25-(GSH)2: A novel curcumin analog. PLoS One., 2014, 9 (9), e107876
DiRaddo, J.; Miller, E.; Hathaway, H.; Grajkowska, E.; Wroblewska, B.; Wolfe, B.; Liotta, D.; Wroblewski, J. A Real-Time Method for Measuring cAMP Production Modulated by Gαi/o-Coupled Metabotropic Glutamate Receptors. J. Pharmacol.Exp. Ther., 2014, 349(3), 373–382.
Hu, H.; Mao, S.; Bugrysheva, J.; Pruett, S.; Liotta, D.; Scott, J.; Snyder, J. Group A streptococcus inhibitors by high-throughput virtual screening. Eur. J. of Med. Chem., 2014, 82, 120-126.
Cox, B.; Prosser, A.; Katzman, B.; Alcaraz, A.; Liotta, D.; Wilson, L.; Snyder, J. Anti-HIV Small Molecule Binding in the Peptide Subpocket of the CXCR4:CVX15 Crystal Structure. Chem. BioChem. 2014, 15(11), 1614-1620.
Krumm S. A.; Yan, D.; Hovingh, E.; Evers, T. J.; Enkirch, T.; Prabhakar R.; Sun, A.; Manohar T.; Arrendale, R.; Painter, G.; Liotta, D..; Natchus, M.; von Messling, V.; Plemper, R. An Orally Available, Small-Molecule Polymerase Inhibitor Shows Efficacy Against a Lethal Morbillivirus Infection in a Large Animal Model. Sci. Transl. Med. 2014, 6(232), p. 232ra52.
Zimmerman, S.; Khatri, A.; Garnier-Amblard, E.; Mullasseril, P.; Kurtkaya, N.; Gyoneva, S.; Hansen, K.; Traynelis, S.; Liotta, D. Design, Synthesis, and Structure–Activity Relationship of a Novel Series of GluN2C-Selective Potentiators. J. Med. Chem. 2014, 57 (6), 2334-2356.
Prosser, A.; Liotta, D. One-pot transformation of esters to analytically pure ketones: methodology and application in process development. Tet. Lett. 2014. Article in Press.
Truax, V.; Zhao, H.; Katzman, B.; Prosser, A.; Alcaraz, A..; Saindane, Manohar T.; Howard, R.; Culver, D.; Arrendale, R.; Gruddanti, P., Taylor J.E., Natchus, M.; Snyder, J.; Liotta, D.; Wilson, L. Discovery of Tetrahydroisoquinoline-Based CXCR4 Antagonists. ACS Med. Chem. Lett. 2013, 4(11), 1025- 1030.
Acker,T.; Khatri, A.; Vance, K.; Slabber, C.; Bacsa, J.; Snyder, J.; Traynelis, S.; Liotta, D. Structure-Activity Relationships and Pharmacophore Model of a Noncompetitive Pyrazoline Page 39 Class of GluN2C/GluN2D Selective Antagonists. J. Med. Chem. 2013, 56(16), 6434-6456.
Moore, T.; Sana, K.; Yan, D.; Krumm, S.; Thepchatri,P.; Snyder, J.; Marengo, J.; Arrendale, R.; Prussia, A.; Natchus, M.; Liotta, D. Synthesis and Metabolic Studies of Host-Directed Inhibitors for Antiviral Therapy. ACS Med. Chem. Lett. 2013, 4(8), 762-767.
Santangelo Freel, R.; Ogden, K..; Strong, K..; Khatri, A.; Chepiga, K..; Jensen, H.; Traynelis, S.; Liotta, D. Synthesis and Structure Activity Relationship of Tetrahydroisoquinoline-Based Potentiators of GluN2C and GluN2D Containing N-Methyl-D-aspartate Receptors. J. Med. Chem. 2013, 56(13), 5351-5381.
Brown, A.; Shi, Q.; Moore, T.; Yoon, Y.; Prussia, A.; Maddox, C.; Liotta, D.; Shim, H.; Snyder, J. Monocarbonyl Curcumin Analogues: Heterocyclic Pleiotropic Kinase Inhibitors That Mediate Anticancer Properties. J. Med. Chem. 2013, 56(9), 3456-3466.
Moore, T.; Sana, K.; Yan, D.;Thepchatri, P.;Ndungu, J.;Sandaine, M.; Lockwood, M.; Natchus, M.; Liotta, D.;Plemper, R.; Snyder, J.; Sun, A. Asymmetric synthesis of host-directed inhibitors of myxovirus. Bellstein J. Org. Chem. 2013, 9(23), 197-203.
Shi, Q.; Moore, T.; Yoon, Y.; Prussia, A.; Maddox, C.; Liotta, D.; Shim, H.; Brown, A.; Snyder, J. Monocarbonyl Curcumin Analogs: Heterocyclic Pleiotropic Kinase Inhibitors that Mediate Anti-Cancer Properties. J. Med. Chem. 2013, 56 (9), 3456-3466.
Kim, J.; Wang, L.; Li, Y.; Becnel, K.; Frey, K.; Garforth, S.; Prasad, V.; Schinazi, R.; Liotta, D.; Anderson, K. Pre-steady State Kinetic Analysis of Cyclobutyl derivatives of 2’-deoxyadenosine 5’-triphosphate as inhibitors of HIC-1 transcriptase. Bioorg. Med. Chem. Lett. 2012, 22(12), 4064-4067.