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Douglas S. Krafte

Observed names: DOUGLAS S. KRAFTE, Doug Krafte, Douglas Krafte, Douglas S Krafte
ORCID: 0000-0002-4667-9069
Observed ORCID: 0000-0002-4667-9069
OpenAlex ID: A5110094654
A-803467, a potent and selective Na v 1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat
2007 · Michael F. Jarvis, Prisca Honore, et al. · Proceedings of the National Academy of Sciences · 536
A rat brain na+ channel α subunit with novel gating properties
1988 · Vanessa J. Auld, Alan L. Goldin, et al. · Neuron · 355
Voltage sensor interaction site for selective small molecule inhibitors of voltage-gated sodium channels
2013 · Ken McCormack, Sonia Santos, et al. · Proceedings of the National Academy of Sciences · 251
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Subtype-Selective Small Molecule Inhibitors Reveal a Fundamental Role for Nav1.7 in Nociceptor Electrogenesis, Axonal Conduction and Presynaptic Release
2016 · Aristos J. Alexandrou, Adam R. Brown, et al. · PLoS ONE · 195
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Involvement of the TTX-resistant sodium channel Nav 1.8 in inflammatory and neuropathic, but not post-operative, pain states
2006 · S. K. Joshi, Joseph P. Mikusa, et al. · Pain · 181
Discovery and Biological Evaluation of 5-Aryl-2-furfuramides, Potent and Selective Blockers of the Nav1.8 Sodium Channel with Efficacy in Models of Neuropathic and Inflammatory Pain
2008 · Michael E. Kort, Irene Drizin, et al. · Journal of Medicinal Chemistry · 89
Distribution and functional properties of human KCNH8 (Elk1) potassium channels
2003 · Anruo Zou, Zhixin Lin, et al. · American Journal of Physiology-Cell Physiology · 66
A-887826 is a structurally novel, potent and voltage-dependent Nav1.8 sodium channel blocker that attenuates neuropathic tactile allodynia in rats
2010 · Xu-Feng Zhang, Char-Chang Shieh, et al. · Neuropharmacology · 60
APOL1-mediated monovalent cation transport contributes to APOL1-mediated podocytopathy in kidney disease
2024 · Somenath Datta, Brett M. Antonio, et al. · Journal of Clinical Investigation · 52
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Direct Activation of an Inwardly Rectifying Potassium Channel by Arachidonic Acid
2001 · Yi Liu, Dong Liu, et al. · Molecular Pharmacology · 44
A comprehensive approach to identifying repurposed drugs to treat SCN 8A epilepsy
2018 · Talia A. Atkin, Chani M. Maher, et al. · Epilepsia · 36
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Novel Inhibitors of Potassium Ion Channels on Human T Lymphocytes
1995 · William F. Michne, Joseph W. Guiles, et al. · Journal of Medicinal Chemistry · 33
Voltage Dependence of Cardiac Delayed Rectifier Block by Methanesulfonamide Class III Antiarrhythmic Agents
1994 · Douglas S. Krafte, Walter A. Volberg · Journal of Cardiovascular Pharmacology · 33
Subtype-selective Nav1.8 sodium channel blockers: Identification of potent, orally active nicotinamide derivatives
2010 · Michael E. Kort, Robert N. Atkinson, et al. · Bioorganic & Medicinal Chemistry Letters · 30
Tenidap, a novel anti-inflammatory agent, is an opener of the inwardly rectifying K+ channel hKir2.3
2002 · Yi Liu, Dong Liu, et al. · European Journal of Pharmacology · 27
Pharmacological modulation of human cardiac Na+ channels
1994 · Douglas S. Krafte, Kathleen Davison, et al. · European Journal of Pharmacology Molecular Pharmacology · 26
Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic pain
2008 · Irene Drizin, Robert J. Gregg, et al. · Bioorganic & Medicinal Chemistry · 24
Expression of functional sodium channels in stage II–III Xenopus oocytes
1989 · Douglas S. Krafte, Henry A. Lester · Journal of Neuroscience Methods · 17
4,5-Dihydro-3-(methanesulfonamidophenyl)-1-phenyl-1H-2,4-benzodiazepines: A Novel Class III Antiarrhythmic Agents
1995 · Robert E. Johnson, Paul J. Silver, et al. · Journal of Medicinal Chemistry · 16
Properties of endogenous voltage-dependent sodium currents in Xenopus laevis oocytes
1992 · Douglas S. Krafte, Walter A. Volberg · Journal of Neuroscience Methods · 14
The Effect of κ-Opioid Receptor Agonists on Tetrodotoxin-Resistant Sodium Channels in Primary Sensory Neurons
2009 · Xin Su, Neil A. Castle, et al. · Anesthesia & Analgesia · 12
[20] Use of stage II–III Xenopus oocytes to study voltage-dependent ion channels
1992 · Douglas S. Krafte, Henry A. Lester · Methods in enzymology on CD-ROM/Methods in enzymology · 11
Decrease of inward rectification as a mechanism for arachidonic acid-induced potentiation of hKir2.3
2002 · Yi Liu, Dong Liu, et al. · European Biophysics Journal · 9
Stable expression and functional characterization of a human cardiac Na+ channel gene in mammalian cells
1995 · Douglas S. Krafte, Walter A. Volberg, et al. · Journal of Molecular and Cellular Cardiology · 9
Pharmacological Regulation of Smooth Muscle by Ion Channels, Kinases, and Cyclic Nucleotides
1996 · Paul J. Silver, Douglas S. Krafte · Elsevier eBooks · 7
Works count: 43
Citation count: 2,171
H-index: 17
I10-index: 22
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