Zobrazeno 1 - 10
of 36
pro vyhledávání: '"W, Petko"'
Autor:
Fernando Camacho, Fink David M, Olsen Gordon Edward, Lawrence L. Martin, Wayne W. Petko, Richard C. Effland, Hugo M. Vargas, Craig P. Smith, David E. Selk, Douglas K. Rush, Klein Joseph Thomas, Peter Allen Nemoto, Larry Davis, Gina M. Bores, James T. Winslow
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:157-162
A series of carbamate analogs of besipirdine (HP 749) was synthesized as potential agents with enhanced cholinomimetic properties for the treatment of Alzheimer's disease. Compound 5a (P10358, 1-[3-fluoro-4-pyridinyl)amino]-3-methyl-1H-indol-5-yl met
Autor:
Roy Corbett, Wayne W. Petko, Gina M. Bores, Ann T. Woods-Kettelberger, Sathapana Kongsamut, Craig P. Smith, Joachim E. Roehr, Susan M. Chesson
Publikováno v:
Neurochemical Research. 21:575-583
Examination of HP 184, [N-n-propyl)-N-(3-fluoro-4-pyridinyl) -1H-3-methylindodel-1-amine hydrochloride], in a variety of tests for serotonergic activity revealed some unique properties of this compound. We report here that 100 microM HP 184 enhanced
Autor:
Kurys Barbara E, Michael C. Merriman, Olsen Gordon Edward, Fink David M, Mark G. Palermo, Francis P. Huger, Gina M. Bores, Wayne W. Petko, Gerard J. O'Malley
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:625-630
A series of imino 1,2,3,4-tetrahydrocyclopent[b]indole carbamates was prepared and evaluated as dual acetylcholinesterase (AChE) and monoamine oxidase (MAO) inhibitors. Halogen substitution ortho to the carbamate functionality in the eight position r
Autor:
Craig P. Smith, Kevin J. Kapples, Michael Cornfeldt, Olsen Gordon Edward, Richard C. Effland, Wayne W. Petko, Klein Joseph Thomas, Francis P. Huger, Larry Davis
Publikováno v:
Journal of Medicinal Chemistry. 39:582-587
A novel series of substituted (pyrroloamino)pyridines was synthesized, and the compounds were evaluated for cholinomimetic-like properties in vitro (inhibition of [3H]quinuclidinyl benzilate binding) and in vivo (reversal of scopolamine-induced demen
Autor:
Richard C. Effland, Craig P. Smith, Joseph Thomas Klein, Joachim E. Roehr, Sathapana Kongsamut, Wayne W. Petko, Francis P. Huger
Publikováno v:
Drug Development Research. 32:13-18
N-(n-propyl)-N-(4-pyridinyl)-1H-indol-1-amine (HP 749) is currently in clinical trials for the treatment of Alzheimer's disease (AD). While HP 749 has many pharmacological properties, the biochemical basis for its efficacy in animal models for AD rem
Autor:
Craig P. Smith, Kevin J. Kapples, Olsen Gordon Edward, Wayne W. Petko, Klein Joseph Thomas, Michael Cornfeldt, Larry Davis, Richard C. Effland, Francis P. Huger
Publikováno v:
ChemInform. 27
A novel series of substituted (pyrroloamino)pyridines was synthesized, and the compounds were evaluated for cholinomimetic-like properties in vitro (inhibition of [3H]quinuclidinyl benzilate binding) and in vivo (reversal of scopolamine-induced demen
Autor:
J. C. Wilker, G. S. Wong, E. Landau, R. D. Blitzer, Richard C. Effland, Lawrence L. Martin, Vahram Haroutunian, Larry Davis, Craig P. Smith, Francis P. Huger, Klein Joseph Thomas, Olsen Gordon Edward, Wayne W. Petko, Michael Cornfeldt
Publikováno v:
ChemInform. 27
Autor:
Klein Joseph Thomas, Craig P. Smith, Fink David M, Wayne W. Petko, Richard C. Effland, Douglas K. Rush, Peter Allen Nemoto, Fernando Camacho, Olsen Gordon Edward, Larry Davis, Gina M. Bores, James T. Winslow, David E. Selk, Hugo M. Vargas, Lawrence L. Martin
Publikováno v:
ChemInform. 28
A series of carbamate analogs of besipirdine (HP 749) was synthesized as potential agents with enhanced cholinomimetic properties for the treatment of Alzheimer's disease. Compound 5a (P10358, 1-[3-fluoro-4-pyridinyl)amino]-3-methyl-1H-indol-5-yl met
Autor:
C P, Smith, G M, Bores, W, Petko, M, Li, D E, Selk, D K, Rush, F, Camacho, J T, Winslow, R, Fishkin, D M, Cunningham, K M, Brooks, J, Roehr, H B, Hartman, L, Davis, H M, Vargas
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 280(2)
1-[(3-Fluoro-4-pyridinyl)amino]-3-methyl-1(H)-indol-5-yl methyl carbamate (P10358) is a potent, reversible acetylcholinesterase inhibitor that produces central cholinergic stimulation after oral and parental administration in rats and mice. P10358 is
Autor:
G M, Bores, F P, Huger, W, Petko, A E, Mutlib, F, Camacho, D K, Rush, D E, Selk, V, Wolf, R W, Kosley, L, Davis, H M, Vargas
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 277(2)
Acetylcholinesterase (AChE) inhibitors from several chemical classes have been tested for the symptomatic treatment of Alzheimer's disease; however, the therapeutic success of these compounds has been limited. Recently, another AChE inhibitor, galant