Elz S - Search Results

1

N(G)-acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the N(G)-substituent.

Igel P, Schneider E, Schnell D, Elz S, Seifert R, Buschauer A. Igel P, et al. Among authors: elz s. J Med Chem. 2009 Apr 23;52(8):2623-7. doi: 10.1021/jm9000693. J Med Chem. 2009. PMID: 19317445

2

Synthesis and pharmacological activity of fluorescent histamine H2 receptor antagonists related to potentidine.

Li L, Kracht J, Peng S, Bernhardt G, Elz S, Buschauer A. Li L, et al. Among authors: elz s. Bioorg Med Chem Lett. 2003 May 19;13(10):1717-20. doi: 10.1016/s0960-894x(03)00235-x. Bioorg Med Chem Lett. 2003. PMID: 12729649

3

N(alpha)-imidazolylalkyl and pyridylalkyl derivatives of histaprodifen: synthesis and in vitro evaluation of highly potent histamine H(1)-receptor agonists.

Menghin S, Pertz HH, Kramer K, Seifert R, Schunack W, Elz S. Menghin S, et al. Among authors: elz s. J Med Chem. 2003 Dec 4;46(25):5458-70. doi: 10.1021/jm0309147. J Med Chem. 2003. PMID: 14640554

4

Structure-activity relationships of histamine H2 receptor ligands.

Dove S, Elz S, Seifert R, Buschauer A. Dove S, et al. Among authors: elz s. Mini Rev Med Chem. 2004 Nov;4(9):941-54. doi: 10.2174/1389557043403242. Mini Rev Med Chem. 2004. PMID: 15544555 Review.

5

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. Ghorai P, et al. Among authors: elz s. J Med Chem. 2008 Nov 27;51(22):7193-204. doi: 10.1021/jm800841w. J Med Chem. 2008. PMID: 18950149

6

Molecular basis for the selective interaction of synthetic agonists with the human histamine H1-receptor compared with the guinea pig H1-receptor.

Strasser A, Wittmann HJ, Kunze M, Elz S, Seifert R. Strasser A, et al. Among authors: elz s. Mol Pharmacol. 2009 Mar;75(3):454-65. doi: 10.1124/mol.108.053009. Epub 2008 Dec 1. Mol Pharmacol. 2009. PMID: 19047480

7

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. Kraus A, et al. Among authors: elz s. ChemMedChem. 2009 Feb;4(2):232-40. doi: 10.1002/cmdc.200800296. ChemMedChem. 2009. PMID: 19072936

8

Chiral NG-acylated hetarylpropylguanidine-type histamine H2 receptor agonists do not show significant stereoselectivity.

Ghorai P, Kraus A, Birnkammer T, Geyer R, Bernhardt G, Dove S, Seifert R, Elz S, Buschauer A. Ghorai P, et al. Among authors: elz s. Bioorg Med Chem Lett. 2010 May 15;20(10):3173-6. doi: 10.1016/j.bmcl.2010.03.082. Epub 2010 Mar 27. Bioorg Med Chem Lett. 2010. PMID: 20409707

9

The bivalent ligand approach leads to highly potent and selective acylguanidine-type histamine H₂ receptor agonists.

Birnkammer T, Spickenreither A, Brunskole I, Lopuch M, Kagermeier N, Bernhardt G, Dove S, Seifert R, Elz S, Buschauer A. Birnkammer T, et al. Among authors: elz s. J Med Chem. 2012 Feb 9;55(3):1147-60. doi: 10.1021/jm201128q. Epub 2012 Jan 25. J Med Chem. 2012. PMID: 22216892

10

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. Hirschfeld J, et al. Among authors: elz s. J Med Chem. 1992 Jun 12;35(12):2231-8. doi: 10.1021/jm00090a013. J Med Chem. 1992. PMID: 1613748

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