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Journal Abstract Search

123 related items for PubMed ID: 11485033

  • 1. Novel histaprodifen analogues as potent histamine H1-receptor agonists in the pithed and in the anaesthetized rat.
    Schlicker E, Kozłowska H, Kwolek G, Malinowska B, Kramer K, Pertz HH, Elz S, Schunack W.
    Naunyn Schmiedebergs Arch Pharmacol; 2001 Jul; 364(1):14-20. PubMed ID: 11485033
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  • 2. Histaprodifen, methylhistaprodifen, and dimethylhistaprodifen are potent H1-receptor agonists in the pithed and in the anaesthetized rat.
    Malinowska B, Piszcz J, Schlicker E, Kramer K, Elz S, Schunack W.
    Naunyn Schmiedebergs Arch Pharmacol; 1999 Jan; 359(1):11-6. PubMed ID: 9933144
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  • 3. Identification of endothelial H1, vascular H2 and cardiac presynaptic H3 receptors in the pithed rat.
    Malinowska B, Schlicker E.
    Naunyn Schmiedebergs Arch Pharmacol; 1993 Jan; 347(1):55-60. PubMed ID: 8383300
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  • 4. Molecular characterization of specific H1-receptor agonists histaprodifen and its Nalpha-substituted analogues on bovine aortic H1-receptors.
    Carman-Krzan M, Bavec A, Zorko M, Schunack W.
    Naunyn Schmiedebergs Arch Pharmacol; 2003 May; 367(5):538-46. PubMed ID: 12669185
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  • 5. Inhibitory H3 receptors on sympathetic nerves of the pithed rat: activation by endogenous histamine and operation in spontaneously hypertensive rats.
    Godlewski G, Malinowska B, Buczko W, Schlicker E.
    Naunyn Schmiedebergs Arch Pharmacol; 1997 Feb; 355(2):261-6. PubMed ID: 9050021
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  • 6. Cardiovascular effects of R-alpha-methylhistamine, a selective histamine H3 receptor agonist, in rats: lack of involvement of histamine H3 receptors.
    Hegde SS, Chan P, Eglen RM.
    Eur J Pharmacol; 1994 Jan 04; 251(1):43-51. PubMed ID: 7907986
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  • 7. Histaprodifens: synthesis, pharmacological in vitro evaluation, and molecular modeling of a new class of highly active and selective histamine H(1)-receptor agonists.
    Elz S, Kramer K, Pertz HH, Detert H, ter Laak AM, Kühne R, Schunack W.
    J Med Chem; 2000 Mar 23; 43(6):1071-84. PubMed ID: 10737740
    [Abstract] [Full Text] [Related]

  • 8. Structure-activity relationships of histamine H1-receptor agonists.
    Pertz HH, Elz S, Schunack W.
    Mini Rev Med Chem; 2004 Nov 23; 4(9):935-40. PubMed ID: 15544554
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  • 9. Contractile properties of various histaprodifen derivatives in guinea pig isolated ileum and trachea.
    Christophe B, Carlier B, Schunack W, Chatelain P, Peck M, Massingham R.
    Pharmacology; 2007 Nov 23; 79(2):104-13. PubMed ID: 17164592
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  • 10. Ring-substituted histaprodifen analogues as partial agonists for histamine H(1) receptors: synthesis and structure-activity relationships.
    Elz S, Kramer K, Leschke C, Schunack W.
    Eur J Med Chem; 2000 Jan 23; 35(1):41-52. PubMed ID: 10733602
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  • 18. Further evidence for the role of histamine H3, but not H1, H2 or H4, receptors in immepip-induced inhibition of the rat cardioaccelerator sympathetic outflow.
    Pinacho-García M, Marichal-Cancino BA, Villalón CM.
    Eur J Pharmacol; 2016 Feb 15; 773():85-92. PubMed ID: 26826593
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  • 19. Role of capsaicin-sensitive nerves and histamine H1, H2, and H3 receptors in the gastroprotective effect of histamine against stress ulcers in rats.
    Dembiński A, Warzecha Z, Ceranowicz P, Brzozowski T, Dembiński M, Konturek SJ, Pawlik WW.
    Eur J Pharmacol; 2005 Jan 31; 508(1-3):211-21. PubMed ID: 15680274
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