Menge WM[au] - Search Results

Year	Number of Results
1994	2
1995	4
1996	2
1997	1
1998	2
1999	6
2000	8
2001	7
2002	1
2003	3
2004	2
2005	3
2006	1
2007	1
2009	1
2015	1
2024	0

1

A third life for burimamide. Discovery and characterization of a novel class of non-opioid analgesics derived from histamine antagonists.

Hough LB, Nalwalk JW, Barnes WG, Leurs R, Menge WM, Timmerman H, Wentland M. Hough LB, et al. Among authors: menge wm. Ann N Y Acad Sci. 2000;909:25-40. doi: 10.1111/j.1749-6632.2000.tb06674.x. Ann N Y Acad Sci. 2000. PMID: 10911922 Review.

2

Antinociceptive activity of furan-containing congeners of improgan and ranitidine.

Hough LB, Menge WM, van de Stolpe AC, Nalwalk JW, Leurs R, de Esch IJ. Hough LB, et al. Among authors: menge wm. Bioorg Med Chem Lett. 2007 Oct 15;17(20):5715-9. doi: 10.1016/j.bmcl.2007.07.060. Epub 2007 Aug 19. Bioorg Med Chem Lett. 2007. PMID: 17766108 Free PMC article.

3

A new potent and selective histamine H3 receptor agonist, 4-(1H-imidazol-4-ylmethyl)piperidine.

Vollinga RC, de Koning JP, Jansen FP, Leurs R, Menge WM, Timmerman H. Vollinga RC, et al. Among authors: menge wm. J Med Chem. 1994 Feb 4;37(3):332-3. doi: 10.1021/jm00029a002. J Med Chem. 1994. PMID: 8308858 No abstract available.

4

New synthetic flavonoids as potent protectors against doxorubicin-induced cardiotoxicity.

van Acker FA, Hulshof JW, Haenen GR, Menge WM, van der Vijgh WJ, Bast A. van Acker FA, et al. Among authors: menge wm. Free Radic Biol Med. 2001 Jul 1;31(1):31-7. doi: 10.1016/s0891-5849(01)00546-9. Free Radic Biol Med. 2001. PMID: 11425487

5

Design, Synthesis, and Evaluation of Linker-Duocarmycin Payloads: Toward Selection of HER2-Targeting Antibody-Drug Conjugate SYD985.

Elgersma RC, Coumans RG, Huijbregts T, Menge WM, Joosten JA, Spijker HJ, de Groot FM, van der Lee MM, Ubink R, van den Dobbelsteen DJ, Egging DF, Dokter WH, Verheijden GF, Lemmens JM, Timmers CM, Beusker PH. Elgersma RC, et al. Among authors: menge wm. Mol Pharm. 2015 Jun 1;12(6):1813-35. doi: 10.1021/mp500781a. Epub 2015 Feb 18. Mol Pharm. 2015. PMID: 25635711

6

Histamine as a marker for hydroxyl radicals.

Ching TL, Hee RM, Bhoelan NM, Blauw J, Menge WM, de Jong J, Bast A. Ching TL, et al. Among authors: menge wm. Mediators Inflamm. 1995;4(5):339-43. doi: 10.1155/S0962935195000548. Mediators Inflamm. 1995. PMID: 18475661 Free PMC article.

7

Fluorescent ligands for the histamine H2 receptor: synthesis and preliminary characterization.

Malan SF, van Marle A, Menge WM, Zuliani V, Hoffman M, Timmerman H, Leurs R. Malan SF, et al. Among authors: menge wm. Bioorg Med Chem. 2004 Dec 15;12(24):6495-503. doi: 10.1016/j.bmc.2004.09.018. Bioorg Med Chem. 2004. PMID: 15556766

8

Evaluation of [18F]VUF 5000 as a potential PET ligand for brain imaging of the histamine H3 receptor.

Windhorst AD, Timmerman H, Klok RP, Menge WM, Leurs R, Herscheid JD. Windhorst AD, et al. Among authors: menge wm. Bioorg Med Chem. 1999 Sep;7(9):1761-7. doi: 10.1016/s0968-0896(99)00108-x. Bioorg Med Chem. 1999. PMID: 10530922

9

Development of a pharmacophore model for histamine H3 receptor antagonists, using the newly developed molecular modeling program SLATE.

De Esch IJ, Mills JE, Perkins TD, Romeo G, Hoffmann M, Wieland K, Leurs R, Menge WM, Nederkoorn PH, Dean PM, Timmerman H. De Esch IJ, et al. Among authors: menge wm. J Med Chem. 2001 May 24;44(11):1666-74. doi: 10.1021/jm001109k. J Med Chem. 2001. PMID: 11356102

10

Clobenpropit analogs as dual activity ligands for the histamine H3 and H4 receptors: synthesis, pharmacological evaluation, and cross-target QSAR studies.

Lim HD, Istyastono EP, van de Stolpe A, Romeo G, Gobbi S, Schepers M, Lahaye R, Menge WM, Zuiderveld OP, Jongejan A, Smits RA, Bakker RA, Haaksma EE, Leurs R, de Esch IJ. Lim HD, et al. Among authors: menge wm. Bioorg Med Chem. 2009 Jun 1;17(11):3987-94. doi: 10.1016/j.bmc.2009.04.007. Epub 2009 Apr 11. Bioorg Med Chem. 2009. PMID: 19414267

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