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Receptors and Channels Volume 10, 2004 - Issue 1
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Original Article

Comparison of the Pharmacological Properties of Rat NaV1.8 with Rat NaV1.2a and Human NaV1.5 Voltage-Gated Sodium Channel Subtypes Using a Membrane Potential Sensitive Dye and FLIPRR

R. G. Vickery Theravance Inc., South San Francisco, CA, USACorrespondenceE-mail: [email protected]
,
S. M. Amagasu Theravance Inc., South San Francisco, CA, USA
,
R. Chang Theravance Inc., South San Francisco, CA, USA
,
N. Mai Theravance Inc., South San Francisco, CA, USA
,
E. Kaufman Theravance Inc., South San Francisco, CA, USA
,
J. Martin Theravance Inc., South San Francisco, CA, USA
,
J. Hembrador Theravance Inc., South San Francisco, CA, USA
,
M. D. O'Keefe Theravance Inc., South San Francisco, CA, USA
,
C. Gee Theravance Inc., South San Francisco, CA, USA
,
D. Marquess Theravance Inc., South San Francisco, CA, USA
&
J. A. M. Smith Theravance Inc., South San Francisco, CA, USA
 show all
Pages 11-23 | Received 01 Mar 2003, Accepted 01 Nov 2003, Published online: 30 Dec 2011

Citations (7)

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Read on this site (2)

Edward C Emery, Ana Paula Luiz & John N Wood. (2016) Nav1.7 and other voltage-gated sodium channels as drug targets for pain relief. Expert Opinion on Therapeutic Targets 20:8, pages 975-983.
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Birgit T Priest & Gregory J Kaczorowski. (2007) Blocking sodium channels to treat neuropathic pain. Expert Opinion on Therapeutic Targets 11:3, pages 291-306.
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Articles from other publishers (5)

Alican Gulsevin, Andrew M. Glazer, Tiffany Shields, Brett M. Kroncke, Dan M. Roden & Jens Meiler. (2022) Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5. International Journal of Molecular Sciences 23:4, pages 2225.
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Yu Du, Emily Days, Ian Romaine, Kris K. Abney, Kristian Kaufmann, Gary Sulikowski, Shaun Stauffer, Craig W. Lindsley & C. David Weaver. (2015) Development and Validation of a Thallium Flux-Based Functional Assay for the Sodium Channel NaV1.7 and Its Utility for Lead Discovery and Compound Profiling. ACS Chemical Neuroscience 6:6, pages 871-878.
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Kun Liu, Manoj Samuel, Jeff Tillett, James K. Hennan, Belew Mekonnen, Veronica Soloveva, Richard K. Harrison, Jeff W. Paslay & James Larocque. (2010) High-Throughput Screening for Kv1.3 Channel Blockers Using an Improved FLIPR-Based Membrane-Potential Assay. SLAS Discovery 15:2, pages 185-195.
Crossref
Mauro Cataldi & Anna Cavaccini. 2010. xPharm: The Comprehensive Pharmacology Reference. xPharm: The Comprehensive Pharmacology Reference 1 26 .
Elfrida R. Benjamin, Farhana Pruthi, Shakira Olanrewaju, Victor I. Ilyin, Gregg Crumley, Elena Kutlina, Kenneth J. Valenzano & Richard M. Woodward. (2006) State-Dependent Compound Inhibition of Nav1.2 Sodium Channels Using the FLIPR Vm Dye: On-Target and Off-Target Effects of Diverse Pharmacological Agents. SLAS Discovery 11:1, pages 29-39.
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