Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Remy David C"'
Autor:
Donald E. Slaughter, Joseph J. Lynch, Roger M. Freidinger, Garry R. Smith, Kamlesh P. Vyas, Remy David C, John J. Baldwin, David A. Pribush, Michael C. Sanguinetti, Stella A. King, Harold G. Selnick, Andrew J. Tebben, Peter K. S. Siegl, David A. Claremon, Elliott Jason M, Nigel J. Liverton, Nancy K. Jurkiewicz, Brian E. Libby, Joseph J. Salata, Charles J. Mcintyre, John W. Butcher
Publikováno v:
Journal of Medicinal Chemistry. 40:3865-3868
Autor:
Kundan P. Doshi, David A. Claremon, Remy David C, Andrew M. Stern, Baldwin John J, Kurt Freund, Steven M. Pitzenberger, Stanley L. Gaul
Publikováno v:
Biochemistry. 33:10109-10119
The physiologic role of several transglutaminases could be more precisely defined with the development of specific inhibitors for these enzymes. In addition, specific plasma transglutaminase (fXIIIa) inhibitors may have therapeutic utility in the tre
Autor:
R. J. Lynch, John J. Baldwin, Remy David C, David A. Claremon, D. J. Armstrong, Nigel J. Liverton, Robert J. Gould, Guixiang Zhang
Publikováno v:
ChemInform. 29
Autor:
R. J. Lynch, Guixiang Zhang, Nigel J. Liverton, Robert J. Gould, Remy David C, Donna J. Armstrong, David A. Claremon, John J. Baldvin
Publikováno v:
Bioorganicmedicinal chemistry letters. 8(5)
The synthesis and biological activity of a series of 3,6-substituted quinazolinediones and quinazolinones are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of these structures as central
Publikováno v:
The Journal of Organic Chemistry. 43:4311-4315
Autor:
David W. Cochran, Remy David C, Stella W. King, James P. Springer, Baldwin John J, Steven D. Young
Publikováno v:
The Journal of Organic Chemistry. 50:339-342
Publikováno v:
Journal of Medicinal Chemistry. 7:1-5
Autor:
Remy David C, Edward L. Engelhardt, Kenneth E. Rittle, Victor J. Lotti, A. Scriabine, Andrew W. Raab
Publikováno v:
Journal of Medicinal Chemistry. 20:836-838
A series of cyproheptadine derivatives having furan nuclei fused to the 10,11-vinylene bridge has been prepared. None of the compounds retain the potent antiserotonin and antihistaminic actions of cyproheptadine. 1-methyl-4-(1-methyl-8H-dibenzo[a,e]f
Autor:
Shebuski, Ronald J., Sitko, Gary R., Claremon, David A., Baldwin, Jack J., Remy, David C., Stern, Andrew M.
Publikováno v:
Blood; April 1990, Vol. 75 Issue: 7 p1455-1459, 5p
Publikováno v:
ChemInform. 19