Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alec Guiblin"'
Autor:
Leslie J. Street, George R. Marshall, Bindi Sohal, Ruth M. McKernan, Andrew Mitchinson, Susan M. Cook, Andrew Pike, José L. Castro, Robert W. Carling, Timothy Harrison, Ian C. Ragan, Sally Ann Thompson, John R. Atack, K Quirk, Andrew Madin, Kevin W. Moore, Michael G. N. Russell, Alec Guiblin, Keith A. Wafford, Gerard R. Dawson, Pushpinder Ferris
Publikováno v:
Journal of Medicinal Chemistry. 48:7089-7092
There is increasing evidence that compounds with selectivity for gamma-aminobutyric acid(A) (GABA(A)) alpha2- and/or alpha3-subtypes may retain the desirable anxiolytic activity of nonselective benzodiazepines but possess an improved side effect prof
Autor:
Alan P. Watt, Susan M. Cook, Alec Guiblin, Christopher Moyes, Ruth M. McKernan, Bindi Sohal, John R. Atack, Luanda J. Pym, Thomas W. Rosahl, Andrew Pike, Paul Scott-Stevens
Publikováno v:
Biopharmaceuticsdrug disposition. 28(6)
The in vivo occupancy of brain benzodiazepine binding sites by compounds A and B was measured using a [3H]Ro 15-1788 binding assay and related to plasma and brain drug concentrations. The plasma concentration associated with 50% occupancy was higher
Autor:
Robert W, Carling, Andrew, Madin, Alec, Guiblin, Michael G N, Russell, Kevin W, Moore, Andrew, Mitchinson, Bindi, Sohal, Andrew, Pike, Susan M, Cook, Ian C, Ragan, Ruth M, McKernan, Kathleen, Quirk, Pushpinder, Ferris, George, Marshall, Sally Ann, Thompson, Keith A, Wafford, Gerard R, Dawson, John R, Atack, Timothy, Harrison, José L, Castro, Leslie J, Street
Publikováno v:
Journal of medicinal chemistry. 48(23)
There is increasing evidence that compounds with selectivity for gamma-aminobutyric acid(A) (GABA(A)) alpha2- and/or alpha3-subtypes may retain the desirable anxiolytic activity of nonselective benzodiazepines but possess an improved side effect prof
Autor:
Leslie J. Street, Francine Sternfeld, Margaret S. Beer, H Routledge, R. Baker, A. P. Watt, Richard Alexander Jelley, Alec Guiblin, W B Davey, Austin John Reeve
Publikováno v:
Journal of medicinal chemistry. 38(10)
The synthesis and the 5-HT receptor activity of a novel series of N,N-dimethyltryptamines substituted in the 5-position with an imidazole, triazole, or tetrazole ring are described. The objective of this work was to identify potent and selective 5-HT