Zobrazeno 1 - 10
of 10
pro vyhledávání: '"G Y, Kuo"'
Autor:
G Y, Kuo, D M, Dulik
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 23(9)
Autor:
Randall K. Johnson, Stanley T. Crooke, Gerald R. Girard, David T. Hill, Leo F. Faucette, G. Y. Kuo, Christopher K. Mirabelli, Sung Cm
Publikováno v:
Journal of Medicinal Chemistry. 29:218-223
A series of gold(I) coordination complexes including analogues of the antiarthritic agent auranofin 1 were evaluated for in vitro cytotoxic potency against both B16 melanoma cells and P388 leukemia cells and in vivo antitumor activity against P388 le
Autor:
P. T. Ridley, Joseph Weinstock, R. A. Hahn, Setler Pe, C. K. Brush, David L. Ladd, James W. Wilson, Holden Kg, Henry M. Sarau, N. C. F. Yim, F. R. Pfeiffer, G. Y. Kuo, A. J. Tobia, Wardell
Publikováno v:
Journal of medicinal chemistry. 23(9)
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 16(6)
Metabolism of ibopamine (N-methyldopamine-O,O'-diisobutyryl ester) was studied in rats and dogs. The compound was well absorbed in both species when given orally. Most of the administered radiolabel (74-94%) was excreted within 24 hr in urine of both
Autor:
Joseph Weinstock, Wardell, James W. Wilson, R. A. Hahn, Paulette E. Setler, Kenneth G. Holden, P. A. Chambers, A. J. Tobia, Henry M. Sarau, F. R. Pfeiffer, G. Y. Kuo
Publikováno v:
Journal of medicinal chemistry. 25(4)
6-Chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines were synthesized and evaluated as agonists of central and peripheral dopamine receptors. These benzazepines were prepared by cyclization of certain amino alcohols followed by demeth
Autor:
David T. Hill, Stanley T. Crooke, Gerald R. Girard, G. Y. Kuo, Leo F. Faucette, Christopher K. Mirabelli, Sung Cm, Randall K. Johnson
Publikováno v:
Chemischer Informationsdienst. 17
A series of gold(I) coordination complexes including analogues of the antiarthritic agent auranofin 1 were evaluated for in vitro cytotoxic potency against both B16 melanoma cells and P388 leukemia cells and in vivo antitumor activity against P388 le
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 15(2)
Both leukotrienes and their receptor antagonists possess substantial pharmacologic activity in in vitro systems, but their duration of action in vivo is extremely short. The exact mechanism of rapid inactivation of these lipids is unknown, but is lik
Autor:
H. M. Sarau, P. A. Chambers, Paulette E. Setler, Joseph Weinstock, G. Y. Kuo, A. J. Tobia, F. R. Pfeiffer, Kenneth G. Holden, James W. Wilson, J. R. Jun. Wardell, R. A. Hahn
Publikováno v:
Chemischer Informationsdienst. 13
Autor:
G. Y. KUO, S. T. ROSS
Publikováno v:
Chemischer Informationsdienst. 10
Autor:
R. A. Hahn, David L. Ladd, J. R. Jun. Wardell, H. M. Sarau, Paulette E. Setler, Kenneth G. Holden, F. R. Pfeiffer, N. C. F. Yim, P. T. Ridley, C. K. Brush, Joseph Weinstock, G. Y. Kuo, James W. Wilson, A. J. Tobia
Publikováno v:
Chemischer Informationsdienst. 12