D. Ngur

发表

Design, synthesis, and neurochemical evaluation of 2-amino-5-(alkoxycarbonyl)-3,4,5,6-tetrahydropyridines and 2-amino-5-(alkoxycarbonyl)-1,4,5,6-tetrahydropyrimidines as M1 muscarinic receptor agonists.

D. A. Smith, P. Dunbar, G. J. Durant, 1994, Journal of medicinal chemistry.

Modulation of GABA-stimulated Cl- flux by a benzodiazepine agonist and an 'inverse agonist' after chronic flurazepam treatment.

T. Chiu, D. Ngur, H. Rosenberg, 1990, European journal of pharmacology.

Stereoselective binding and activity of oxotremorine analogs at muscarinic receptors in rat brain.

W. Hoss, U. Hacksell, P. Dunbar, 1992, Chirality.

Studies on the pharmacology of d-amphetamine on maximal electroconvulsive seizure in young chicks

D. Ngur, G. Osuide, C. Wambebe, 2004, Psychopharmacology.

Synthesis, biochemical activity and behavioral effects of a series of 1,4,5,6-tetrahydropyrimidines as novel ligands for M1 receptors

W. Hoss, K. Ryan, P. Dunbar, 1992 .

Synthesis and biological characterization of 1,4,5,6-tetrahydropyrimidine and 2-amino-3,4,5,6-tetrahydropyridine derivatives as selective m1 agonists.

P. Dunbar, T. Rho, B. Ojo, 1997, Journal of medicinal chemistry.

Design, synthesis, and neurochemical evaluation of 5-(3-alkyl-1,2,4- oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidines as M1 muscarinic receptor agonists.

W. Hoss, P. Dunbar, G. J. Durant, 1993, Journal of Medicinal Chemistry.

High-performance liquid chromatographic study of the photochemical oxidation of vasicine and its analogues.

D. Ngur, S. K. Hirani, B. K. Chowdhury, 1987, Journal of chromatography.

Synthesis and biochemical activity of novel amidine derivatives as m1 muscarinic receptor agonists.

W. Hoss, P. Dunbar, G. J. Durant, 1996, Bioorganic & medicinal chemistry.

Steric and electronic requirements for muscarinic receptor-stimulated phosphoinositide turnover in the CNS in a series of arecoline bioisosteres.

W. Hoss, C. Mitch, S. Quimby, 1992, Biochemical and biophysical research communications.