BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 1687832)

  • 1. Synthesis and histamine H2-agonistic activity of ring-substituted phenyl analogues of impromidine.
    Buschauer A; Lachenmayr F; Schunack W
    Pharmazie; 1991 Dec; 46(12):840-5. PubMed ID: 1687832
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and histamine H2-receptor activity of heterocyclic impromidine analogues.
    Buschauer A; Lachenmayr F; Schunack W
    Pharmazie; 1992 Feb; 47(2):86-91. PubMed ID: 1353262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effects of impromidine- and arpromidine-derived guanidines on recombinant human and guinea pig histamine H1 and H2 receptors.
    Xie SX; Schalkhausser F; Ye QZ; Seifert R; Buschauer A
    Arch Pharm (Weinheim); 2007 Jan; 340(1):9-16. PubMed ID: 17206612
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Synthesis and pharmacologic action of substituted imidazolyl- and thiazolylmethylthioethylguanidine].
    Buschauer A
    Arzneimittelforschung; 1987 Sep; 37(9):1003-7. PubMed ID: 2893625
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis and in vitro pharmacology of arpromidine and related phenyl(pyridylalkyl)guanidines, a potential new class of positive inotropic drugs.
    Buschauer A
    J Med Chem; 1989 Aug; 32(8):1963-70. PubMed ID: 2569042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Impromidine-analogous guanidines: synthesis and activity at the histamine H2-receptor. 29. Histamine analogs].
    Elz S; Schunack W
    Arzneimittelforschung; 1988 Mar; 38(3):327-32. PubMed ID: 2898245
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structure-activity relationships of histamine H2-agonists, a new class of positive inotropic drugs.
    Buschauer A; Baumann G
    Agents Actions Suppl; 1991; 33():231-56. PubMed ID: 1828931
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Synthesis and pharmacologic action of arylmethylethylguanidines].
    Buschauer A
    Arzneimittelforschung; 1987 Sep; 37(9):1008-12. PubMed ID: 2893626
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [H2-antagonistic activity of the impromidine analog, cyanoguanidine. 37. H2 antihistaminics].
    Elz S; Schunack W
    Arzneimittelforschung; 1988 Jan; 38(1):7-10. PubMed ID: 2896510
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of histamine H2-receptors in human neutrophils with a series of guanidine analogues of impromidine. Are cell type-specific H2-receptors involved in the regulation of NADPH oxidase?
    Burde R; Buschauer A; Seifert R
    Naunyn Schmiedebergs Arch Pharmacol; 1990 May; 341(5):455-61. PubMed ID: 1694972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 4- or 5- (omega-aminoalkyl) thiazoles and derivatives; new selective H2-receptor agonists.
    Eriks JC; Sterk GJ; van der Aar EM; van Acker SA; van der Goot H; Timmerman H
    Agents Actions Suppl; 1991; 33():301-14. PubMed ID: 1828933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Histamine analogues. 36th communication. Basically substituted histamine derivatives with H1-agonistic activity.
    Zingel V; Elz S; Schunack W
    Pharmazie; 1992 Oct; 47(10):746-51. PubMed ID: 1480650
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Iodoaminopotentidine and related compounds: a new class of ligands with high affinity and selectivity for the histamine H2 receptor.
    Hirschfeld J; Buschauer A; Elz S; Schunack W; Ruat M; Traiffort E; Schwartz JC
    J Med Chem; 1992 Jun; 35(12):2231-8. PubMed ID: 1613748
    [TBL] [Abstract][Full Text] [Related]  

  • 14. N1-(3-cyclohexylbutanoyl)-N2-[3-(1H-imidazol-4-yl)propyl]guanidine (UR-AK57), a potent partial agonist for the human histamine H1- and H2-receptors.
    Xie SX; Kraus A; Ghorai P; Ye QZ; Elz S; Buschauer A; Seifert R
    J Pharmacol Exp Ther; 2006 Jun; 317(3):1262-8. PubMed ID: 16554355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence for histamine H1 and H2 receptors in guinea-pig oxyntic cells.
    Vinik AI; Heldsinger AA; Skoglund ML
    J Pharmacol Exp Ther; 1983 Oct; 227(1):115-21. PubMed ID: 6137553
    [TBL] [Abstract][Full Text] [Related]  

  • 16. N(G)-acylated aminothiazolylpropylguanidines as potent and selective histamine H(2) receptor agonists.
    Kraus A; Ghorai P; Birnkammer T; Schnell D; Elz S; Seifert R; Dove S; Bernhardt G; Buschauer A
    ChemMedChem; 2009 Feb; 4(2):232-40. PubMed ID: 19072936
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acylguanidines as bioisosteres of guanidines: NG-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists.
    Ghorai P; Kraus A; Keller M; Götte C; Igel P; Schneider E; Schnell D; Bernhardt G; Dove S; Zabel M; Elz S; Seifert R; Buschauer A
    J Med Chem; 2008 Nov; 51(22):7193-204. PubMed ID: 18950149
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Synthesis and biological activity of substituted 2-(4-imidazolyl)ethylamines].
    Plazzi PV; Bordi F; Vitto M; Impicciatore M
    Farmaco Sci; 1981 Nov; 36(11):931-31. PubMed ID: 6118297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Probing ligand-specific histamine H1- and H2-receptor conformations with NG-acylated Imidazolylpropylguanidines.
    Xie SX; Ghorai P; Ye QZ; Buschauer A; Seifert R
    J Pharmacol Exp Ther; 2006 Apr; 317(1):139-46. PubMed ID: 16394198
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Therapeutic value of H2-receptor stimulation in congestive heart failure. Hemodynamic effects of BU-E-76, BU-E-75 and arpromidine (BU-E-50) in comparison to impromidine.
    Felix SB; Buschauer A; Baumann G
    Agents Actions Suppl; 1991; 33():257-69. PubMed ID: 1828932
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.