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Page 1
Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists.
Quattropani A, Dorbais J, Covini D, Pittet PA, Colovray V, Thomas RJ, Coxhead R, Halazy S, Scheer A, Missotten M, Ayala G, Bradshaw C, De Raemy-Schenk AM, Nichols A, Cirillo R, Tos EG, Giachetti C, Golzio L, Marinelli P, Church DJ, Barberis C, Chollet A, Schwarz MK. Quattropani A, et al. Among authors: church dj. J Med Chem. 2005 Dec 1;48(24):7882-905. doi: 10.1021/jm050645f. J Med Chem. 2005. PMID: 16302826
Design, synthesis, and biological activity of novel, potent, and selective (benzoylaminomethyl)thiophene sulfonamide inhibitors of c-Jun-N-terminal kinase.
Rückle T, Biamonte M, Grippi-Vallotton T, Arkinstall S, Cambet Y, Camps M, Chabert C, Church DJ, Halazy S, Jiang X, Martinou I, Nichols A, Sauer W, Gotteland JP. Rückle T, et al. Among authors: church dj. J Med Chem. 2004 Dec 30;47(27):6921-34. doi: 10.1021/jm031112e. J Med Chem. 2004. PMID: 15615541
Fragment analysis in small molecule discovery.
Merlot C, Domine D, Church DJ. Merlot C, et al. Among authors: church dj. Curr Opin Drug Discov Devel. 2002 May;5(3):391-9. Curr Opin Drug Discov Devel. 2002. PMID: 12058614 Review.
Chemical substructures in drug discovery.
Merlot C, Domine D, Cleva C, Church DJ. Merlot C, et al. Among authors: church dj. Drug Discov Today. 2003 Jul 1;8(13):594-602. doi: 10.1016/s1359-6446(03)02740-5. Drug Discov Today. 2003. PMID: 12850335 Review.
Cellular assays of chemokine receptor activation.
Proudfoot AE, Power CA, Church DJ, Soler D, Mack M. Proudfoot AE, et al. Among authors: church dj. Curr Protoc Pharmacol. 2001 Nov;Chapter 12:Unit12.4. doi: 10.1002/0471141755.ph1204s14. Curr Protoc Pharmacol. 2001. PMID: 21959755
26 results