Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Albert Braunwalder"'
Autor:
Albert Braunwalder, Michael Williams
Publikováno v:
Journal of Neurochemistry. 47:88-97
Adenine nucleotides displace the binding of the selective adenosine A-1 receptor ligand [3H]cyclopentyladenosine (CPA) to rat brain membranes in a concentration-dependent manner, with the rank order of activity being ATP greater than ADP greater than
Autor:
W. D. Cash, Albert Braunwalder, P.S. Bernard, G. C. Mazzenga, R. A. Lovell, B. S. Barbaz, Francis John E, J. L. Hyun, Debra A. Bennett, R. C. Friedmann, P. S. Loo
Publikováno v:
ChemInform. 22
Publikováno v:
Analytical biochemistry. 238(2)
A nonradioactive, sensitive assay method to evaluate the activity of protein tyrosine kinases is described. This method utilizes europium chelate-labeled anti-phosphotyrosine antibodies to detect phosphate transfer to a polymeric substrate coated ont
Autor:
James Wasvary, Isidoros Vlattas, James L. Stanton, Albert Braunwalder, Bruce Seligmann, Matthew A. Sills, James Dellureficio, Galakatos Nicholas G, Richard Kramer, Iou Iou Sytwu
Publikováno v:
Journal of medicinal chemistry. 37(17)
In order to identify regions of C5a that contribute to receptor binding and functional activity of the anaphylatoxin, a series of peptides was synthesized in which core segments have been attached to C-terminal segments via native peptidic or disulfi
Autor:
Galakatos Nicholas G, Matthew J. Toth, William O. Haston, Matthew A. Sills, Donna R. Yarwood, Bruce Seligmann, Albert Braunwalder, William C. Boyar, Leslie Huwyler, Joseph T. Hadala
We have determined which amino acids contribute to the pharmacophore of human C5a, a potent inflammatory mediator. A systematic mutational analysis of this 74-amino acid protein was performed and the effects on the potency of receptor binding and of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b77975a36b4e3a2a39e16669dc49efbe
https://europepmc.org/articles/PMC2142918/
https://europepmc.org/articles/PMC2142918/
Autor:
Shou-Ih Hu, Lynnette Conder, Sid Vlattas, Albert Braunwalder, Catherine L. Cioffi, Lawrence P. Wennogle, Richard Kramer, Cindy Winter
Publikováno v:
Journal of cellular biochemistry. 55(3)
Binding of biotin-C5a to the C5a receptor in membrane fragments followed by detergent solubilization and purification with streptavidin-agarose affinity chromatography resulted in the isolation of a receptor complex with associated G-proteins. In con
Autor:
R. A. Lovell, J. L. Hyun, R. C. Friedmann, Francis John E, P. S. Loo, P.S. Bernard, G. C. Mazzenga, B. S. Barbaz, W. D. Cash, Albert Braunwalder
Publikováno v:
Journal of medicinal chemistry. 34(1)
Investigation of tricyclic heterocycles related to the 2-arylpyrazolo[4,3-c]quinolin-3(5H)-ones, structures with high affinity for the benzodiazepine (BZ) receptor, led to the synthesis of 2-phenyl-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one, a compou
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 332:179-183
The binding of [3H]-Cyclopentyladenosine (CPA), an N6-substituted analog of adenosine, was examined in vitro. CPA bound with high affinity (Kd = 0.48 nmol/l) to rat brain membranes. Specific binding, which represented 90-97% of the total counts bound
Autor:
P.S. Bernard, Susan Gerhardt, Patricia Loo, Jeffrey M. Liebman, Naokata Yokoyama, Caryl L. Amrick, Carl A. Boast, Markus Schmutz, Albert Braunwalder, D. Wilson, Debra A. Bennett, Klaus Klebs
Publikováno v:
Drug Development Research. 11:219-233
CGS 17867A (2-(4-chlorophenyl)-2,5,6,7,8,9,-hexahydor-3H-pyrazolo [4,3,-c]quinoline-3-one-hydrochloride salt) is a tetrahydorpyrazoloquinoline related to the benzodiazepine (BZ) receptor agonist, CGS 9896. The compound is an effective inhibitor of [3
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 8:785-788
The efficacy of coupling between the benzodiazepine receptor and chloride channel as well as the coupling to the GABA receptor is differentially affected by different benzodiazepine ligands. In general, the order of efficacy with regard to allosteric