Search Results - "Reischer, R J"

Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus influenzae and Moraxella catarrhalis by GENIN, Michael J., ALLWINE, Debra A., ANDERSON, David J., BARBACHYN, Michael R., EMMERT, D. Edward, GARMON, Stuart A., GRABER, David R., GREGA, Kevin C., HESTER, Jackson B., HUTCHINSON, Douglas K., MORRIS, Joel, REISCHER, Robert J., FORD, Charles W., ZURENKO, Gary E., HAMEL, Judith C., SCHAADT, Ronda D., STAPERT, Douglas, YAGI, Betty H.

“…A series of new nitrogen-carbon-linked (azolylphenyl)oxazolidinone antibacterial agents has been prepared in an effort to expand the spectrum of activity of…”
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Isomeric inversion of ibuprofen (R)-enantiomer in humans by Kaiser, D G, Vangiessen, G J, Reischer, R J, Wechter, W J

“…Enantiomeric compositions of the major urinary metabolites of ibuprofen [(RS)-2-(4-isobutylphenyl)propionic acid]were characterized after oral administration…”
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A new affinity label for guanosine nucleotide sites in proteins by Pal, P K, Reischer, R J, Wechter, W J, Colman, R F

“…A new guanosine analogue has been synthesized, 5'-p-fluorosulfonylbenzoyl guanosine, which has an electrophilic moiety capable of reacting covalently with…”
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Enzymatic inversion at saturated carbon: nature and mechanism of the inversion of R(-) p-iso-butyl hydratropic acid by Wechter, W J, Loughhead, D G, Reischer, R J, VanGiessen, G J, Kaiser, D G

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Design, synthesis, and evaluation of novel oxazolidinone antibacterial agents active against multidrug-resistant bacteria by Barbachyn, M R, Brickner, S J, Gadwood, R C, Garmon, S A, Grega, K C, Hutchinson, D K, Munesada, K, Reischer, R J, Taniguchi, M, Thomasco, L M, Toops, D S, Yamada, H, Ford, C W, Zurenko, G E

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Structure-Based Design of Nonpeptidic HIV Protease Inhibitors:  The Sulfonamide-Substituted Cyclooctylpyranones by Skulnick, Harvey I, Johnson, Paul D, Aristoff, Paul A, Morris, Jeanette K, Lovasz, Kristine D, Howe, W. Jeffrey, Watenpaugh, Keith D, Janakiraman, Musiri N, Anderson, David J, Reischer, Robert J, Schwartz, Theresa M, Banitt, Lee S, Tomich, Paul K, Lynn, Janet C, Horng, Miao-Miao, Chong, Kong-Teck, Hinshaw, Roger R, Dolak, Lester A, Seest, Eric P, Schwende, Francis J, Rush, Bob D, Howard, Gina M, Toth, Lisa N, Wilkinson, Karen R, Kakuk, Thomas J, Johnson, Carol W, Cole, Serena L, Zaya, Renee M, Zipp, Gail L, Possert, Peggy L, Dalga, Robert J, Zhong, Wei-Zhu, Williams, Marta G, Romines, Karen R

“…Recently, cyclooctylpyranone derivatives with m-carboxamide substituents (e.g. 2c) were identified as potent, nonpeptidic HIV protease inhibitors, but these…”
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Structure-based design of nonpeptidic HIV protease inhibitors: the sulfonamide-substituted cyclooctylpyramones by Skulnick, H I, Johnson, P D, Aristoff, P A, Morris, J K, Lovasz, K D, Howe, W J, Watenpaugh, K D, Janakiraman, M N, Anderson, D J, Reischer, R J, Schwartz, T M, Banitt, L S, Tomich, P K, Lynn, J C, Horng, M M, Chong, K T, Hinshaw, R R, Dolak, L A, Seest, E P, Schwende, F J, Rush, B D, Howard, G M, Toth, L N, Wilkinson, K R, Romines, K R

“…Recently, cyclooctylpyranone derivatives with m-carboxamide substituents (e.g. 2c) were identified as potent, nonpeptidic HIV protease inhibitors, but these…”
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