Zobrazeno 1 - 10
of 28
pro vyhledávání: '"C S, Rooney"'
Autor:
Julie A. O'Brien, A. M. Smith, C. S. Rooney, John S. Wai, Jacob M. Hoffman, J. H. Nunberg, Thorsten E. Fisher, P. S. Anderson, M. E. Goldman, A. M. Stern, C. M. Thomas, Quintero Julio C, W. S. Saari, Emilio A. Emini, William A. Schleif
Publikováno v:
ChemInform. 23
Autor:
W. S. Saari, J. H. Nunberg, Jacob M. Hoffman, Julie A. O'Brien, P. S. Anderson, J. H. Jones, Thorsten E. Fisher, M. E. Goldman, A. M. Smith, Quintero Julio C, C. M. Thomas, C. S. Rooney, William A. Schleif, Dona L. Bamberger, John S. Wai, Emilio A. Emini
Publikováno v:
ChemInform. 24
Autor:
Julie A. O'Brien, M E Goldman, S K Balani, V V Sardana, Terrence M. Ciccarone, C. S. Rooney, S. C. Mactough, Jon H. Condra, P. S. Anderson, William A. Schleif, Theresa M. Williams, Emilio A. Emini, Theoharides Anthony D, L. R. Kauffman, William J. Greenlee
Publikováno v:
ChemInform. 25
Autor:
John S. Wai, R. J. Hudcosky, Theresa M. Williams, Jacob M. Hoffman, J. H. Nunberg, S. C. Mactough, Quintero Julio C, W. S. Saari, P. S. Anderson, M. E. Goldman, Emilio A. Emini, William A. Schleif, C. M. Thomas, C. S. Rooney, Thorsten E. Fisher, Dona L. Bamberger, Julie A. O'Brien
Publikováno v:
ChemInform. 25
Autor:
S K, Balani, L R, Kauffman, B H, Arison, T V, Olah, M E, Goldman, S L, Varga, J A, O'Brien, H G, Ramjit, C S, Rooney, J M, Hoffman
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 22(2)
Healthy subjects were administered single oral doses of 800 mg or 400 mg 3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methylpyridin-2(1H)-o ne (L-696,229), a nonnucleoside inhibitor of the human immunodeficiency virus-type 1 (HIV-1) reverse transcriptase (
Autor:
S K, Balani, S M, Pitzenberger, L R, Kauffman, B H, Arison, H G, Ramjit, M E, Goldman, J A, O'Brien, J D, King, J M, Hoffman, C S, Rooney
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 20(6)
L-696,229 is a potent and specific inhibitor of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase and is currently undergoing clinical evaluation. In vivo metabolism in rats was investigated using an intravenous bolus dose of 5 mg/kg
Publikováno v:
Canadian Journal of Chemistry. 53:2279-2292
A series of 3-substituted-aminomethy1-3-hydroxy-3,4-dihydro-2H-1,5-benzodioxepins is described. Members of the series constitute a unique class of β-adrenergic stimulants and possess interesting bronchial dilator activity.
Autor:
C. S. Rooney, H. W. R. Williams
Publikováno v:
Synthetic Communications. 7:201-213
Currently, there is considerable interest in the synthesis of peptide derivatives bearing an aldehyde at the C-terminal position in place of the carboxyl group1,2. This interest may have arisen from, and been intensified by, the identification of sev
Publikováno v:
The Journal of Antibiotics. 42:30-36
In freshly harvested Aspergillus terreus cultures grown for the production of lovastatin (formerly called mevinolin), no monacolin L could be detected. However, during the isolation of lovastatin, significant quantities of monacolin L appeared. It ha
Autor:
C. S. Rooney, A. N. Bourns
Publikováno v:
Canadian Journal of Chemistry. 33:1633-1637
p-Trifluoromethyltolane and p-fluorotolane have been synthesized by the action of sodium or potassium amide in liquid ammonia on para-substituted 1,1-diphenyl-2-bromoethylenes. The geometrical isomers of 1-(p-trifluoromethylphenyl)-1-phenyl-2-bromoet