Upload
greg-bisacchi
View
23
Download
4
Embed Size (px)
Citation preview
RESEARCH ARTICLES, REVIEWS, AND BOOK CHAPTERS (partial list)
41. Bisacchi, G. S. “Recreating the golden age of antibiotics” Manuscript in preparation
40. Bisacchi, G. S. and Hale, M. “A double-edged” scaffold: antitumor power within the antibacterial quinolone.” Manuscript in review.
39. Bisacchi, G. S. “Origins of the quinolone class of antibacterials: an expanded “drug discovery story”. J. Med. Chem. 2015 DOI: 10.1021/jm501881c
38. Bisacchi, G. S. and Manchester, J. I. “A new-class antibacterial--almost. Lessons in drug discovery and development: a crucial analysis of more than 50 years of effort toward ATPase inhibitors of DNA gyrase and topoisomerase IV” ACS Infectious Diseases 2015, 1, 4-41. DOI: 10.1021/id500013t
37. Hangeland, J. J.; Friends, T. J.; Rossi, K. A.; Smallheer, J. M.; Wang, C.; Sun, Z.; Corte, J. R.; Fang, T.; Wong, P. C.; Rendina, A. R.; Barbera, F. A.; Bozarth, J. M.; Luettgen, J. M.; Watson, C. A.; Zhang, G.; Wei, A.; Ramamurthy, V.; Morin, P. E.; Bisacchi, G. S.; Subramaniam, S.; Arunachalam, P.; Mathur, A.; Seiffert, D. A.; Wexler, R. R.; Quan, M. L. “Phenylimidazoles as Potent and Selective Inhibitors of Coagulation Factor XIa with In Vivo Antithrombotic Activity” J. Med. Chem., 2014, 57, DOI: 10.10/21/jm5010607
36. Bolton S. A.; Sutton J. C.; Anumula R.; Bisacchi G.S.; Jacobson B.; Slusarchyk W. A.; Treuner U. D.; Wu S. C.; Zhao G.; Pi Z.; Sheriff S.; Smirk R. A.; Bisaha S.; Cheney D. L.; Wei A.; Schumacher W. A.; Hartl K. S.; Liu E.; Zahler R.; Seiler S. M. “Discovery of Nonbenzamidine Factor VIIa Inhibitors Using a Biaryl Acid Scaffold” Bioorganic & Medicinal Chemistry Letters 2013, 23, 5239-5243.
35. Manchester, J.; Buurman, E. T.; Bisacchi, G. S.; McLaughlin, R. E. “Molecular Determinants of AcrB-Mediated Bacterial Efflux: Implications for Drug Discovery” J. Med. Chem., 2012, 55, 2532-2537.
34. Bisacchi, G. S. and Dumas, J. “Recent Advances in the Inhibition of Bacterial Type II Topoisomerases” in Annual Reports in Medicinal Chemistry, Volume 44, Macor, J., Ed, Elsevier, 2009.
33. Sherawat, M.; Kaur, P.; Perbandt, M.; Betzel, C.; Slusarchyk, W. A.; Bisacchi, G. S.; Chang, C.; Jacobson, B. L.; Einspahr, H. M.; Singh, T. P. “Crystal Structure of the Complex Formed Between Trypsin and a Designed Synthetic Highly Potent Inhibitor in the Presence of Benzamidine at 0.97A Resolution” Acta Crystallographica 2007, Section D: Biological Crystallography, D63(4), 500-507.
32. Shi, Y.; Zhang, J.; Stein, P. D.; Shi, M.; O’Connor, S. P.; Bisaha, S. N.; Li, C.; Atwal, K.; Bisacchi, G.; Sitkoff, D.; Pudzianowski, A. T.; Liu, E. C.; Hartl, K. S.; Seiler, S. M.; Youssef, S.; Setinbacher, T. E.; Schumacher, W. A.; Rendina, A. R.; Bozarth. J. M.; Peterson, T. L.; Zhang, G.; Zaher, R.; “Kenene Aminal-based Lactam Derivatives as a Novel Class of Orally Active FXa Inhibitiors” Bioorganic & Medicinal Chemistry Letters 2005, 15(24), 5453-5458.
31. Bisacchi, G. S.; Stein, P. D.; Gougoutas, J. Z.; Hartl, K. S.; Lawrence, R. M.; Liu, E.; Pudzianowski, A.; Schumacher, W. A.; Sitkoff, D.; Steinbacher, T. E.; Sutton, J.; Zhang, Z.;
Page 2 of 2
Seiler, S. M. “Initial Structure-Activity Relationships for a Caprolactam-based Series of Neutral Factor Xa Inhibitors: Lead Identification” Letters in Drug Design and Discovery 2005, 2(8), 625-630.
30. Bisacchi, G. S.; Slusarchyk, W. A.; Bolton, S. A.; Hartl, K. S.; Jacobs, G.; Mathur, A.; Meng, W.; Ogletree, M. L.; Pi. Z.; Sutton, J. C.; Treuner, U.; Zahler, R.; Zhao, G.; Seiler, S. M. “Synthesis of Potent and Highly Selective Non-Guanidine Azetidinone Inhibitors of Human Tryptase” Bioorganic & Medicinal Chemistry Letters 2004, 14, 2227-2231.
29. Sutton, J. C.; Bolton, S. A.; Davis, M. E.; Hartl, K. S.; Jacobson, B.; Mathur, A.; Ogletree, M. L.; Slusarchyk, W. A.; Zahler, R.; Seiler, S. M.; Bisacchi, G. S. “Solid Phase Synthesis and SAR of 4-Carboxy-2-Azetidinone Mechanism-Based Tryptase Inhibitors” Bioorganic & Medicinal Chemistry Letters 2004 14, 2233-2239.
28. Washburn, W. N.; Sun, C.-Q.; Bisacchi, G. S.; Wu. G.; Cheng, P. T.; Sher, P. M.; Ryono, D.; Gavai, A. V.; Poss, K.; Girotra, R. N.; McCann, P. J.; Mikkilineni, A. B.; Dejneka, T. C.; Wang, T. C.; Merchant, Z.; Morella, M.; Arbeeny, C. M.; Harper, T. W.; Slusarchyk, D. A.; Skwish, S.; Russell, A. D.; Allen, G. T.; Tesfamariam, B.; Frohlich, B. H.; Abboa-Offei, B. E.; Cap, M.; Waldron, T. L.; George, R. J.; Young, D.; Dickinson, K. E.; Seymour, A. A. “BMS-201620: a Selective Beta 3 Agonist” Bioorganic & Medicinal Chemistry Letters 2004, 14, 3525-3529.
27. Zhao, G.; Bolton, S. A., Kwon, C.; Hartl, K. S.; Seiler, S. A.; Slusarchyk, S. A.; Sutton, J. C.; Bisacchi, G. S. “Synthesis of Potent and Selective 2-Azepanone Inhibitors of Human Tryptase” Bioorganic & Medicinal Chemistry Letters 2004, 14, 309-312.
26. Bisacchi, G. S. “Anticoagulants, Antithrombotics, and Hemostatics” in Burger’s Medicinal Chemistry and Drug Discovery, 6th Ed., Vol. 3: Therapeutic Agents, Abraham, D., Ed., John Wiley, 2003.
25. Sutton, J. C.; Bolton, S. A.; Hartl, K.S.; Huang, M.-H.; Jacobs, G.; Meng, W.; Ogletree, M.; Pi, Z.; Schumacher, W. A.; Seiler, S. M.; Slusarchyk, W. A.; Treuner, W.; Zahler, R.; Zhao, G.; Bisacchi, G. S. “Synthesis and SAR of 4-Carboxy-2-azetidinone Mechanism-Based Tryptase Inhibitors” Bioorganic & Medicinal Chemistry Letters 2002, 12, 3229-3233.
24. Slusarchyk, W. A.; Bolton, S. A.; Hartl, K. A.; Huang, M.-H.; Jacobs, G.; Meng, W.; Ogletree, M. L.; Pi, Z.; Schumacher, W. A.; Seiler, S. M.; Sutton, J. C.; Treuner, U.; Zahler, R.; Zhao, G.; Bisacchi, G. S. “Synthesis of Potent and Highly Selective Inhibitors of Human Tryptase” Bioorganic & Medicinal Chemistry Letters 2002, 12, 3235-3238.
23. Chen, B.-C.; Bednarz, M. S.; Sundeen, J. E.; Zhang, Z. J.; Caufield, T. J.; Bisacchi, G. S. "An Improved Large Scale Synthesis of 2,3-Dihydroxyterephthalic Acid and Dimethyl 2,3-Dihydroxyterephthalate" Org. Prep Proced. Int. 1999, 31, 106-109.
22. Yamanaka, G.; Wilson, T.; Innaimo, S.; Bisacchi, G. S.; Egli, P.; Rinehart, J. K.; Zahler,R.; Colonno, R. J. “Metabolic Studies on BMS-200475, a New Antiviral Compound Active Against Hepatitis B. Virus” Antimicrobial Agents Chemother. 1999, 43, 190-193.