Valentin K. Gribkoff
Affiliations: | Knopp Neurosciences Inc., Pittsburgh, PA, United States |
Google:
"Valentin Gribkoff"Mean distance: 14.19 (cluster 19) | S | N | B | C | P |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Sacchetti S, Dworetzky SI, Alavian KN, et al. (2011) Decrease in a Leak Conductance Associated with Mitochondrial Complex V and Improved Bioenergetic Efficiency may Underlie Cytoprotection of at-Risk Neurons by Dexpramipexole Biophysical Journal. 100: 459a |
Romine JL, Martin SW, Meanwell NA, et al. (2007) 3-[(5-Chloro-2-hydroxyphenyl)methyl]-5-[4-(trifluoromethyl)phenyl ]-1,3,4-oxadiazol-2(3H)-one, BMS-191011: opener of large-conductance Ca(2+)-activated potassium (maxi-K) channels, identification, solubility, and SAR. Journal of Medicinal Chemistry. 50: 528-42 |
Lindner MD, Hogan JB, Hodges DB, et al. (2006) Donepezil primarily attenuates scopolamine-induced deficits in psychomotor function, with moderate effects on simple conditioning and attention, and small effects on working memory and spatial mapping. Psychopharmacology. 188: 629-40 |
Yang B, Gribkoff VK, Pan J, et al. (2006) Pharmacological activation and inhibition of Slack (Slo2.2) channels. Neuropharmacology. 51: 896-906 |
Lindner MD, Hogan JB, Krause RG, et al. (2006) Soluble Abeta and cognitive function in aged F-344 rats and Tg2576 mice. Behavioural Brain Research. 173: 62-75 |
Vrudhula VM, Dasgupta B, Boissard CG, et al. (2005) Analogs of a potent maxi-K potassium channel opener with an improved inhibitory profile toward cytochrome P450 isozymes. Bioorganic & Medicinal Chemistry Letters. 15: 4286-90 |
Gribkoff VK, Winquist RJ. (2005) Voltage-gated cation channel modulators for the treatment of stroke. Expert Opinion On Investigational Drugs. 14: 579-92 |
Boy KM, Guernon JM, Sit SY, et al. (2004) 3-Thio-quinolinone maxi-K openers for the treatment of erectile dysfunction. Bioorganic & Medicinal Chemistry Letters. 14: 5089-93 |
Wu YJ, He H, Sun LQ, et al. (2004) Synthesis and structure-activity relationship of acrylamides as KCNQ2 potassium channel openers. Journal of Medicinal Chemistry. 47: 2887-96 |
Wu YJ, Boissard CG, Chen J, et al. (2004) (S)-N-[1-(4-cyclopropylmethyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-ethyl]-3-(2-fluoro-phenyl)-acrylamide is a potent and efficacious KCNQ2 opener which inhibits induced hyperexcitability of rat hippocampal neurons. Bioorganic & Medicinal Chemistry Letters. 14: 1991-5 |