Schmutz M - Search Results

1

Quinazolinedione sulfonamides: a novel class of competitive AMPA receptor antagonists with oral activity.

Koller M, Lingenhoehl K, Schmutz M, Vranesic IT, Kallen J, Auberson YP, Carcache DA, Mattes H, Ofner S, Orain D, Urwyler S. Koller M, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 2011 Jun 1;21(11):3358-61. doi: 10.1016/j.bmcl.2011.04.017. Epub 2011 Apr 8. Bioorg Med Chem Lett. 2011. PMID: 21531559

2

5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition.

Auberson YP, Allgeier H, Bischoff S, Lingenhoehl K, Moretti R, Schmutz M. Auberson YP, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 2002 Apr 8;12(7):1099-102. doi: 10.1016/s0960-894x(02)00074-4. Bioorg Med Chem Lett. 2002. PMID: 11909726

3

AMPA receptor antagonists: potential therapeutic applications.

Mattes H, Lingenhoehl K, Kalkman H, Auberson Y, Renaud J, Schmutz M, Orain D. Mattes H, et al. Among authors: schmutz m. Recent Pat CNS Drug Discov. 2006 Nov;1(3):247-59. doi: 10.2174/157488906778773698. Recent Pat CNS Drug Discov. 2006. PMID: 18221206 Review.

4

5-Aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists.

Acklin P, Allgeier H, Auberson YP, Bischoff S, Ofner S, Sauer D, Schmutz M. Acklin P, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 1998 Mar 3;8(5):493-8. doi: 10.1016/s0960-894x(98)00055-9. Bioorg Med Chem Lett. 1998. PMID: 9871605

5

5-Aminomethylquinoxaline-2,3-diones. Part I: A novel class of AMPA receptor antagonists.

Auberson YP, Bischoff S, Moretti R, Schmutz M, Veenstra SJ. Auberson YP, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 1998 Jan 6;8(1):65-70. doi: 10.1016/s0960-894x(97)10186-x. Bioorg Med Chem Lett. 1998. PMID: 9871630

6

N-phosphonoalkyl-5-aminomethylquinoxaline-2,3-diones: in vivo active AMPA and NMDA(glycine) antagonists.

Auberson YP, Acklin P, Bischoff S, Moretti R, Ofner S, Schmutz M, Veenstra SJ. Auberson YP, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 1999 Jan 18;9(2):249-54. doi: 10.1016/s0960-894x(98)00720-3. Bioorg Med Chem Lett. 1999. PMID: 10021939

7

Synthesis, radiolabelling and biological characterization of (D)-7-iodo-N-(1-phosphonoethyl)-5-aminomethylquinoxaline-2,3-dione, a glycine-binding site antagonist of NMDA receptors.

Ametamey SM, Kokic M, Carrey-Rémy N, Bläuenstein P, Willmann M, Bischoff S, Schmutz M, Schubiger PA, Auberson YP. Ametamey SM, et al. Among authors: schmutz m. Bioorg Med Chem Lett. 2000 Jan 3;10(1):75-8. doi: 10.1016/s0960-894x(99)00576-4. Bioorg Med Chem Lett. 2000. PMID: 10636248

8

(R,S)-4-phosphonophenylglycine, a potent and selective group III metabotropic glutamate receptor agonist, is anticonvulsive and neuroprotective in vivo.

Gasparini F, Bruno V, Battaglia G, Lukic S, Leonhardt T, Inderbitzin W, Laurie D, Sommer B, Varney MA, Hess SD, Johnson EC, Kuhn R, Urwyler S, Sauer D, Portet C, Schmutz M, Nicoletti F, Flor PJ. Gasparini F, et al. Among authors: schmutz m. J Pharmacol Exp Ther. 1999 Jun;289(3):1678-87. J Pharmacol Exp Ther. 1999. PMID: 10336568

9

CGP 37849 and CGP 39551: novel and potent competitive N-methyl-D-aspartate receptor antagonists with oral activity.

Fagg GE, Olpe HR, Pozza MF, Baud J, Steinmann M, Schmutz M, Portet C, Baumann P, Thedinga K, Bittiger H, et al. Fagg GE, et al. Among authors: schmutz m. Br J Pharmacol. 1990 Apr;99(4):791-7. doi: 10.1111/j.1476-5381.1990.tb13008.x. Br J Pharmacol. 1990. PMID: 1972895 Free PMC article.

10

CGP 37849 and CGP 39551: novel competitive N-methyl-D-aspartate receptor antagonists with potent oral anticonvulsant activity.

Fagg GE, Olpe HR, Schmutz M, Pozza MF, van Riezen H, Bittiger H, Angst C, Brundish D, Allgeier H, Heckendorn R, et al. Fagg GE, et al. Among authors: schmutz m. Prog Clin Biol Res. 1990;361:421-7. Prog Clin Biol Res. 1990. PMID: 1981260 Review. No abstract available.

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