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Brian E Marron

Showing results (1-10 of 16) with videos related to

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Current Opinion in Chemical Biology|June 27, 2003
Going to the well no more: lawn format assays for ultra-high-throughput screeningBrian E Marron, Channa K Jayawickreme
Channels (Austin, Tex.)|December 10, 2015
Voltage gated sodium channels as drug discovery targetsSharan K Bagal, Brian E Marron, Robert M Owen, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2014
Recent progress in sodium channel modulators for painSharan K Bagal, Mark L Chapman, Brian E Marron, et al.
ACS Medicinal Chemistry Letters|April 16, 2021
Discovery of the First Orally Available, Selective K<sub>Na</sub>1.1 Inhibitor: <i>In Vitro</i> and <i>In Vivo</i> Activity of an Oxadiazole SeriesAndrew M Griffin, Kristopher M Kahlig, Robert John Hatch, et al.
Neuropharmacology|June 23, 2010
A-887826 is a structurally novel, potent and voltage-dependent Na(v)1.8 sodium channel blocker that attenuates neuropathic tactile allodynia in ratsXu-Feng Zhang, Char-Chang Shieh, Mark L Chapman, et al.
ACS Medicinal Chemistry Letters|June 20, 2017
Discovery of a Series of Indazole TRPA1 AntagonistsDavid C Pryde, Brian E Marron, Christopher W West, et al.
Journal of Combinatorial Chemistry|March 11, 2003
High-throughput manual parallel synthesis using SynPhase crowns and lanternsSamuel W Gerritz, Mark H Norman, Lee A Barger, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 3, 2013
Voltage sensor interaction site for selective small molecule inhibitors of voltage-gated sodium channelsKen McCormack, Sonia Santos, Mark L Chapman, et al.
ACS Chemical Neuroscience|March 28, 2020
Discovery, Radiolabeling, and Evaluation of Subtype-Selective Inhibitors for Positron Emission Tomography Imaging of Brain Phosphodiesterase-4DYuichi Wakabayashi, Sanjay Telu, Rachel M Dick, et al.
Bioorganic & Medicinal Chemistry|October 23, 2010
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic painMarc J C Scanio, Lei Shi, Irene Drizin, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Current Opinion in Chemical Biology|June 27, 2003
Going to the well no more: lawn format assays for ultra-high-throughput screeningBrian E Marron, Channa K Jayawickreme
Channels (Austin, Tex.)|December 10, 2015
Voltage gated sodium channels as drug discovery targetsSharan K Bagal, Brian E Marron, Robert M Owen, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2014
Recent progress in sodium channel modulators for painSharan K Bagal, Mark L Chapman, Brian E Marron, et al.
ACS Medicinal Chemistry Letters|April 16, 2021
Discovery of the First Orally Available, Selective K<sub>Na</sub>1.1 Inhibitor: <i>In Vitro</i> and <i>In Vivo</i> Activity of an Oxadiazole SeriesAndrew M Griffin, Kristopher M Kahlig, Robert John Hatch, et al.
Neuropharmacology|June 23, 2010
A-887826 is a structurally novel, potent and voltage-dependent Na(v)1.8 sodium channel blocker that attenuates neuropathic tactile allodynia in ratsXu-Feng Zhang, Char-Chang Shieh, Mark L Chapman, et al.
ACS Medicinal Chemistry Letters|June 20, 2017
Discovery of a Series of Indazole TRPA1 AntagonistsDavid C Pryde, Brian E Marron, Christopher W West, et al.
Journal of Combinatorial Chemistry|March 11, 2003
High-throughput manual parallel synthesis using SynPhase crowns and lanternsSamuel W Gerritz, Mark H Norman, Lee A Barger, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 3, 2013
Voltage sensor interaction site for selective small molecule inhibitors of voltage-gated sodium channelsKen McCormack, Sonia Santos, Mark L Chapman, et al.
ACS Chemical Neuroscience|March 28, 2020
Discovery, Radiolabeling, and Evaluation of Subtype-Selective Inhibitors for Positron Emission Tomography Imaging of Brain Phosphodiesterase-4DYuichi Wakabayashi, Sanjay Telu, Rachel M Dick, et al.
Bioorganic & Medicinal Chemistry|October 23, 2010
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic painMarc J C Scanio, Lei Shi, Irene Drizin, et al.
Pageof 2