Gnerre C - Search Results

1

Inhibition of monoamine oxidases by functionalized coumarin derivatives: biological activities, QSARs, and 3D-QSARs.

Gnerre C, Catto M, Leonetti F, Weber P, Carrupt PA, Altomare C, Carotti A, Testa B. Gnerre C, et al. J Med Chem. 2000 Dec 14;43(25):4747-58. doi: 10.1021/jm001028o. J Med Chem. 2000. PMID: 11123983

2

Interaction of psychotropic drugs with monoamine oxidase in rat brain.

Gnerre C, Kosel M, Baumann P, Carrupt PA, Testa B. Gnerre C, et al. J Pharm Pharmacol. 2001 Aug;53(8):1125-30. doi: 10.1211/0022357011776513. J Pharm Pharmacol. 2001. PMID: 11518022

3

Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studies.

Carotti A, Carrieri A, Chimichi S, Boccalini M, Cosimelli B, Gnerre C, Carotti A, Carrupt PA, Testa B. Carotti A, et al. Among authors: gnerre c. Bioorg Med Chem Lett. 2002 Dec 16;12(24):3551-5. doi: 10.1016/s0960-894x(02)00798-9. Bioorg Med Chem Lett. 2002. PMID: 12443774

4

Lipophilicity plays a major role in modulating the inhibition of monoamine oxidase B by 7-substituted coumarins.

Carotti A, Altomare C, Catto M, Gnerre C, Summo L, De Marco A, Rose S, Jenner P, Testa B. Carotti A, et al. Among authors: gnerre c. Chem Biodivers. 2006 Feb;3(2):134-49. doi: 10.1002/cbdv.200690017. Chem Biodivers. 2006. PMID: 17193252

5

Monoamine oxidase inhibitory activity of some Hypericum species native to South Brazil.

Gnerre C, von Poser GL, Ferraz A, Viana A, Testa B, Rates SM. Gnerre C, et al. J Pharm Pharmacol. 2001 Sep;53(9):1273-9. doi: 10.1211/0022357011776568. J Pharm Pharmacol. 2001. PMID: 11578110

6

Monoamine oxidase inhibitor properties of some benzazoles: structure-activity relationships.

Grandi T, Sparatore F, Gnerre C, Crivori P, Carrupt PA, Testa B. Grandi T, et al. Among authors: gnerre c. AAPS PharmSci. 1999;1(4):E16. doi: 10.1208/ps010416. AAPS PharmSci. 1999. PMID: 11741212 Free PMC article.

7

In vitro biotransformation of the selective serotonin reuptake inhibitor citalopram, its enantiomers and demethylated metabolites by monoamine oxidase in rat and human brain preparations.

Kosel M, Gnerre C, Voirol P, Amey M, Rochat B, Bouras C, Testa B, Baumann P. Kosel M, et al. Among authors: gnerre c. Mol Psychiatry. 2002;7(2):181-8. doi: 10.1038/sj.mp.4000946. Mol Psychiatry. 2002. PMID: 11840311

8

Novel 2-(2-(benzylthio)-1H-benzo[d]imidazol-1-yl)acetic acids: discovery and hit-to-lead evolution of a selective CRTh2 receptor antagonist chemotype.

Pothier J, Riederer MA, Peter O, Leroy X, Valdenaire A, Gnerre C, Fretz H. Pothier J, et al. Among authors: gnerre c. Bioorg Med Chem Lett. 2012 Jul 15;22(14):4660-4. doi: 10.1016/j.bmcl.2012.05.087. Epub 2012 Jun 1. Bioorg Med Chem Lett. 2012. PMID: 22726929

9

Evolution of novel tricyclic CRTh2 receptor antagonists from a (E)-2-cyano-3-(1H-indol-3-yl)acrylamide scaffold.

Valdenaire A, Pothier J, Renneberg D, Riederer MA, Peter O, Leroy X, Gnerre C, Fretz H. Valdenaire A, et al. Among authors: gnerre c. Bioorg Med Chem Lett. 2013 Feb 15;23(4):944-8. doi: 10.1016/j.bmcl.2012.12.050. Epub 2012 Dec 25. Bioorg Med Chem Lett. 2013. PMID: 23324405

10

Discovery of the Potent, Selective, Orally Available CXCR7 Antagonist ACT-1004-1239.

Richard-Bildstein S, Aissaoui H, Pothier J, Schäfer G, Gnerre C, Lindenberg E, Lehembre F, Pouzol L, Guerry P. Richard-Bildstein S, et al. Among authors: gnerre c. J Med Chem. 2020 Dec 24;63(24):15864-15882. doi: 10.1021/acs.jmedchem.0c01588. Epub 2020 Dec 14. J Med Chem. 2020. PMID: 33314938

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