Zobrazeno 1 - 5
of 5
pro vyhledávání: '"R J Reischer"'
Autor:
Gary E. Zurenko, Betty H. Yagi, Douglas K Hutchinson, D E Emmert, David R. Graber, Jackson B. Hester, Stuart A. Garmon, Judith C. Hamel, Michael R Barbachyn, Ronda D. Schaadt, Michael J. Genin, Douglas Stapert, Joel Morris, David J. Anderson, Debra A. Allwine, R J Reischer, Charles W. Ford, Kevin C. Grega
Publikováno v:
Journal of Medicinal Chemistry. 43:953-970
A series of new nitrogen-carbon-linked (azolylphenyl)oxazolidinone antibacterial agents has been prepared in an effort to expand the spectrum of activity of this class of antibiotics to include Gram-negative organisms. Pyrrole, pyrazole, imidazole, t
Autor:
M R, Barbachyn, S J, Brickner, R C, Gadwood, S A, Garmon, K C, Grega, D K, Hutchinson, K, Munesada, R J, Reischer, M, Taniguchi, L M, Thomasco, D S, Toops, H, Yamada, C W, Ford, G E, Zurenko
Publikováno v:
Advances in experimental medicine and biology. 456
Autor:
G.L Zipp, Lester A. Dolak, K. D. Watenpaugh, W.-Z Zhong, R. R. Hinshaw, C.W Johnson, David J. Anderson, L. S. Banitt, Johnson Paul D, Paul A. Aristoff, G.M Howard, M.N. Janakiraman, R J Reischer, Howe Wj, Harvey Irving Skulnick, Theresa M. Schwartz, L. N. Toth, K.R Wilkinson, Bob D. Rush, Karen Rene Romines, J. C. Lynn, Serena L. Cole, M. G. Williams, Eric P. Seest, Renee M. Zaya, Joel Morris, Chong Kt, Thomas J. Kakuk, R.J Dalga, K D Lovasz, Tomich Pk, M.‐M. Horng, P.L Possert, F.J Schwende
Publikováno v:
Journal of medicinal chemistry. 40(7)
Recently, cyclooctylpyranone derivatives with m-carboxamide substituents (e.g. 2c) were identified as potent, nonpeptidic HIV protease inhibitors, but these compounds lacked significant antiviral activity in cell culture. Substitution of a sulfonamid
Publikováno v:
Journal of Biological Chemistry. 253:6644-6646
A new guanosine analogue has been synthesized, 5'-p-fluorosulfonylbenzoyl guanosine, which has an electrophilic moiety capable of reacting covalently with several classes of amino acid side chains found in proteins. This compound reacts with bovine l
Publikováno v:
The Journal of biological chemistry. 253(19)
A new guanosine analogue has been synthesized, 5'-p-fluorosulfonylbenzoyl guanosine, which has an electrophilic moiety capable of reacting covalently with several classes of amino acid side chains found in proteins. This compound reacts with bovine l