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Free Radical Biology & Medicine|June 27, 2001
New synthetic flavonoids as potent protectors against doxorubicin-induced cardiotoxicityF A van Acker, J W Hulshof, G R Haenen, et al.Brain Research|December 5, 1998
Absence of antinociceptive tolerance to improgan, a cimetidine analog, in ratsM D Bannoura, J W Nalwalk, Y Tang, et al.Journal of Medicinal Chemistry|October 6, 2000
Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activityF A van Acker, J A Hageman, G R Haenen, et al.Journal of Medicinal Chemistry|May 5, 2000
Characterization of the binding site of the histamine H(3) receptor. 2. Synthesis, in vitro pharmacology, and QSAR of a series of monosubstituted benzyl analogues of thioperamideA D Windhorst, H Timmerman, E A Worthington, et al.The Journal of Pharmacology and Experimental Therapeutics|February 12, 1998
Novel qualitative structure-activity relationships for the antinociceptive actions of H2 antagonists, H3 antagonists and derivativesL B Hough, J W Nalwalk, B Y Li, et al.Brain Research|October 18, 2000
Improgan, a cimetidine analog, induces morphine-like antinociception in opioid receptor-knockout miceL B Hough, J W Nalwalk, Y Chen, 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.Journal of Medicinal Chemistry|May 18, 2001
Development of a pharmacophore model for histamine H3 receptor antagonists, using the newly developed molecular modeling program SLATEI J De Esch, J E Mills, T D Perkins, et al.Journal of Medicinal Chemistry|April 10, 1999
Characterization of the binding site of the histamine H3 receptor. 1. Various approaches to the synthesis of 2-(1H-imidazol-4-yl)cyclopropylamine and histaminergic activity of (1R,2R)- and (1S,2S)-2-(1H-imidazol-4-yl)-cyclopropylamineI J De Esch, R C Vollinga, K Goubitz, et al.Nuclear Medicine and Biology|December 10, 1999
Radiosynthesis and biodistribution of 123I-labeled antagonists of the histamine H3 receptor as potential SPECT ligandsA D Windhorst, H Timmerman, R P Klok, et al.Pageof 4