Odermatt A - Search Results

1

In silico methods in the discovery of endocrine disrupting chemicals.

Vuorinen A, Odermatt A, Schuster D. Vuorinen A, et al. Among authors: odermatt a. J Steroid Biochem Mol Biol. 2013 Sep;137:18-26. doi: 10.1016/j.jsbmb.2013.04.009. Epub 2013 May 17. J Steroid Biochem Mol Biol. 2013. PMID: 23688835 Review.

2

Comparative enzymology of 11beta-hydroxysteroid dehydrogenase type 1 from six species.

Arampatzis S, Kadereit B, Schuster D, Balazs Z, Schweizer RA, Frey FJ, Langer T, Odermatt A. Arampatzis S, et al. Among authors: odermatt a. J Mol Endocrinol. 2005 Aug;35(1):89-101. doi: 10.1677/jme.1.01736. J Mol Endocrinol. 2005. PMID: 16087724

3

Why is 11beta-hydroxysteroid dehydrogenase type 1 facing the endoplasmic reticulum lumen? Physiological relevance of the membrane topology of 11beta-HSD1.

Odermatt A, Atanasov AG, Balazs Z, Schweizer RA, Nashev LG, Schuster D, Langer T. Odermatt A, et al. Mol Cell Endocrinol. 2006 Mar 27;248(1-2):15-23. doi: 10.1016/j.mce.2005.11.040. Epub 2006 Jan 10. Mol Cell Endocrinol. 2006. PMID: 16412558 Review.

4

The discovery of new 11beta-hydroxysteroid dehydrogenase type 1 inhibitors by common feature pharmacophore modeling and virtual screening.

Schuster D, Maurer EM, Laggner C, Nashev LG, Wilckens T, Langer T, Odermatt A. Schuster D, et al. Among authors: odermatt a. J Med Chem. 2006 Jun 15;49(12):3454-66. doi: 10.1021/jm0600794. J Med Chem. 2006. PMID: 16759088

5

Discovery of nonsteroidal 17beta-hydroxysteroid dehydrogenase 1 inhibitors by pharmacophore-based screening of virtual compound libraries.

Schuster D, Nashev LG, Kirchmair J, Laggner C, Wolber G, Langer T, Odermatt A. Schuster D, et al. Among authors: odermatt a. J Med Chem. 2008 Jul 24;51(14):4188-99. doi: 10.1021/jm800054h. Epub 2008 Jun 6. J Med Chem. 2008. PMID: 18533708

6

Selective inhibition of 11beta-hydroxysteroid dehydrogenase 1 by 18alpha-glycyrrhetinic acid but not 18beta-glycyrrhetinic acid.

Classen-Houben D, Schuster D, Da Cunha T, Odermatt A, Wolber G, Jordis U, Kueenburg B. Classen-Houben D, et al. Among authors: odermatt a. J Steroid Biochem Mol Biol. 2009 Feb;113(3-5):248-52. doi: 10.1016/j.jsbmb.2009.01.009. Epub 2009 Feb 7. J Steroid Biochem Mol Biol. 2009. PMID: 19429429

7

The UV-filter benzophenone-1 inhibits 17beta-hydroxysteroid dehydrogenase type 3: Virtual screening as a strategy to identify potential endocrine disrupting chemicals.

Nashev LG, Schuster D, Laggner C, Sodha S, Langer T, Wolber G, Odermatt A. Nashev LG, et al. Among authors: odermatt a. Biochem Pharmacol. 2010 Apr 15;79(8):1189-99. doi: 10.1016/j.bcp.2009.12.005. Epub 2009 Dec 11. Biochem Pharmacol. 2010. PMID: 20005209

8

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches.

Rollinger JM, Kratschmar DV, Schuster D, Pfisterer PH, Gumy C, Aubry EM, Brandstötter S, Stuppner H, Wolber G, Odermatt A. Rollinger JM, et al. Among authors: odermatt a. Bioorg Med Chem. 2010 Feb 15;18(4):1507-15. doi: 10.1016/j.bmc.2010.01.010. Epub 2010 Jan 11. Bioorg Med Chem. 2010. PMID: 20100662

9

Characterization of activity and binding mode of glycyrrhetinic acid derivatives inhibiting 11β-hydroxysteroid dehydrogenase type 2.

Kratschmar DV, Vuorinen A, Da Cunha T, Wolber G, Classen-Houben D, Doblhoff O, Schuster D, Odermatt A. Kratschmar DV, et al. Among authors: odermatt a. J Steroid Biochem Mol Biol. 2011 May;125(1-2):129-42. doi: 10.1016/j.jsbmb.2010.12.019. Epub 2011 Jan 12. J Steroid Biochem Mol Biol. 2011. PMID: 21236343

10

Identification of chemically diverse, novel inhibitors of 17β-hydroxysteroid dehydrogenase type 3 and 5 by pharmacophore-based virtual screening.

Schuster D, Kowalik D, Kirchmair J, Laggner C, Markt P, Aebischer-Gumy C, Ströhle F, Möller G, Wolber G, Wilckens T, Langer T, Odermatt A, Adamski J. Schuster D, et al. Among authors: odermatt a. J Steroid Biochem Mol Biol. 2011 May;125(1-2):148-61. doi: 10.1016/j.jsbmb.2011.01.016. Epub 2011 Feb 12. J Steroid Biochem Mol Biol. 2011. PMID: 21300150

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