Sigurd Elz - Search Results

Year	Number of Results
2002	3
2003	4
2004	2
2005	1
2006	5
2007	2
2008	4
2009	3
2010	2
2011	5
2012	1
2013	2
2014	2
2015	2
2016	2
2018	3
2019	1
2020	2
2021	1
2024	0

1

Structure-activity relationships of histamine H1-receptor agonists.

Pertz HH, Elz S, Schunack W. Pertz HH, et al. Among authors: elz s. Mini Rev Med Chem. 2004 Nov;4(9):935-40. doi: 10.2174/1389557043403198. Mini Rev Med Chem. 2004. PMID: 15544554 Review.

2

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.

3

Structure-Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands^†.

Pockes S, Wifling D, Buschauer A, Elz S. Pockes S, et al. Among authors: elz s. ChemistryOpen. 2019 Mar 5;8(3):285-297. doi: 10.1002/open.201900011. eCollection 2019 Mar. ChemistryOpen. 2019. PMID: 30886786 Free PMC article.

4

Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors.

Sellmer A, Stangl H, Beyer M, Grünstein E, Leonhardt M, Pongratz H, Eichhorn E, Elz S, Striegl B, Jenei-Lanzl Z, Dove S, Straub RH, Krämer OH, Mahboobi S. Sellmer A, et al. Among authors: elz s. J Med Chem. 2018 Apr 26;61(8):3454-3477. doi: 10.1021/acs.jmedchem.7b01593. Epub 2018 Apr 6. J Med Chem. 2018. PMID: 29589441

5

Design and biological evaluation of tetrahydro-β-carboline derivatives as highly potent histone deacetylase 6 (HDAC6) inhibitors.

Leonhardt M, Sellmer A, Krämer OH, Dove S, Elz S, Kraus B, Beyer M, Mahboobi S. Leonhardt M, et al. Among authors: elz s. Eur J Med Chem. 2018 May 25;152:329-357. doi: 10.1016/j.ejmech.2018.04.046. Epub 2018 Apr 26. Eur J Med Chem. 2018. PMID: 29738953

6

Mepyramine-JNJ7777120-hybrid compounds show high affinity to hH(1)R, but low affinity to hH(4)R.

Wagner E, Wittmann HJ, Elz S, Strasser A. Wagner E, et al. Among authors: elz s. Bioorg Med Chem Lett. 2011 Nov 1;21(21):6274-80. doi: 10.1016/j.bmcl.2011.09.001. Epub 2011 Sep 8. Bioorg Med Chem Lett. 2011. PMID: 21944853

7

A series of novel aryl-methanone derivatives as inhibitors of FMS-like tyrosine kinase 3 (FLT3) in FLT3-ITD-positive acute myeloid leukemia.

Sellmer A, Pilsl B, Beyer M, Pongratz H, Wirth L, Elz S, Dove S, Henninger SJ, Spiekermann K, Polzer H, Klaeger S, Kuster B, Böhmer FD, Fiebig HH, Krämer OH, Mahboobi S. Sellmer A, et al. Among authors: elz s. Eur J Med Chem. 2020 May 1;193:112232. doi: 10.1016/j.ejmech.2020.112232. Epub 2020 Mar 13. Eur J Med Chem. 2020. PMID: 32199135

8

Theoretical studies on the interaction of partial agonists with the 5-HT2A receptor.

Silva ME, Heim R, Strasser A, Elz S, Dove S. Silva ME, et al. Among authors: elz s. J Comput Aided Mol Des. 2011 Jan;25(1):51-66. doi: 10.1007/s10822-010-9400-2. Epub 2010 Nov 19. J Comput Aided Mol Des. 2011. PMID: 21088982

9

Frontiers in medicinal chemistry in Regensburg.

Dove S, Seifert R, Elz S, Buschauer A. Dove S, et al. Among authors: elz s. ChemMedChem. 2008 Aug;3(8):1181-4. doi: 10.1002/cmdc.200800114. ChemMedChem. 2008. PMID: 18655207 No abstract available.

10

Structural modifications in the distal, regulatory region of histamine H₃ receptor antagonists leading to the identification of a potent anti-obesity agent.

Szczepańska K, Pockes S, Podlewska S, Höring C, Mika K, Latacz G, Bednarski M, Siwek A, Karcz T, Nagl M, Bresinsky M, Mönnich D, Seibel U, Kuder KJ, Kotańska M, Stark H, Elz S, Kieć-Kononowicz K. Szczepańska K, et al. Among authors: elz s. Eur J Med Chem. 2021 Mar 5;213:113041. doi: 10.1016/j.ejmech.2020.113041. Epub 2020 Nov 24. Eur J Med Chem. 2021. PMID: 33261900

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