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Bioorganic & Medicinal Chemistry Letters|December 3, 2014
Design and synthesis of novel small molecule CCR2 antagonists: evaluation of 4-aminopiperidine derivativesM Vilums, A J M Zweemer, S Dekkers, et al.European Journal of Pharmacology|April 23, 1997
Mutational analysis of the putative devazepide binding site of the CCK(A) receptorR L Smeets, A P IJzerman, H P Hermsen, et al.Journal of Medicinal Chemistry|June 8, 2000
Isoquinoline and quinazoline urea analogues as antagonists for the human adenosine A(3) receptorJ E van Muijlwijk-Koezen, H Timmerman, H van der Goot, et al.British Journal of Pharmacology|January 1, 1995
Pharmacological and biochemical analysis of FPL 67156, a novel, selective inhibitor of ecto-ATPaseB E Crack, C E Pollard, M W Beukers, et al.Bioorganic & Medicinal Chemistry Letters|December 21, 2010
Structure-activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A)J P D van Veldhoven, C C Blad, C M Artsen, et al.Journal of Medicinal Chemistry|August 22, 2003
Pyrazole derivatives as partial agonists for the nicotinic acid receptorT van Herk, J Brussee, A M C H van den Nieuwendijk, et al.British Journal of Pharmacology|July 7, 2017
Correlation between human ether-a-go-go-related gene channel inhibition and action potential prolongationP Saxena, M P Hortigon-Vinagre, S Beyl, et al.Journal of Medicinal Chemistry|November 26, 1997
N6-cyclopentyl-3'-substituted-xylofuranosyladenosines: a new class of non-xanthine adenosine A1 receptor antagonistsS Van Calenbergh, J K von Frijtag Drabbe Künzel, N M Blaton, et al.Scientific Reports|December 13, 2022
Pan-cancer functional analysis of somatic mutations in G protein-coupled receptorsB J Bongers, M Gorostiola González, X Wang, et al.Biochemical and Biophysical Research Communications|November 19, 2016
Small molecule absorption by PDMS in the context of drug response bioassaysB J van Meer, H de Vries, K S A Firth, et al.Pageof 14