A small family of novel 2,4(5)-diarylimidazoles were prepared through a simple and efficient synthesis and evaluated as potential inhibitors of hNav1.2 sodium channel currents. One member of this series (4) exhibited profound inhibition of Nav1.2 currents, emerging as a promising lead compound for further structure–activity relationship studies for the development of novel sodium channel blockers
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na$_V$) chan...
In the present investigation, the rationale for the design, synthesis, and biological evaluation of ...
Previously identified potent and/or use-dependent mexiletine (Mex) analogs were used as template for...
Sodium (Na) channels continue to represent an important target for the development of novel anticonv...
2,4(1H)-Diarylimidazoles have been previously shown to inhibit hNaV1.2 sodium (Na) channel currents....
We previously reported the discovery of diphenylimidazoles as potent sodium channel blockers, potent...
2,4(1H)-Diarylimidazoles have been previously shown to inhibit hNaV1.2 sodium (Na) channel currents....
Voltage-gated sodium channels play an integral part in neurotransmission and their dysfunction is fr...
We previously reported that a lipophilic N-(4'-hydroxy-3',5'-di-tert-butylbenzyl) derivative (1) of ...
We have synthesized and evaluated a series of 1,4-disubstituted-triazole derivatives for inhibition ...
Sponges of the genus Agelas produce compounds that modulate the activity of voltage-gated sodium ion...
Voltage-gated sodium channels (VGSC) are responsible for the selective influx of sodium ions in exci...
Voltage-gated sodium channels (VGSC) are responsible for the selective influx of sodium ions in exci...
Drug screening on sodium currents of native myofibers by means of voltage-clamp recordings is predic...
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (NaV) channel...
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na$_V$) chan...
In the present investigation, the rationale for the design, synthesis, and biological evaluation of ...
Previously identified potent and/or use-dependent mexiletine (Mex) analogs were used as template for...
Sodium (Na) channels continue to represent an important target for the development of novel anticonv...
2,4(1H)-Diarylimidazoles have been previously shown to inhibit hNaV1.2 sodium (Na) channel currents....
We previously reported the discovery of diphenylimidazoles as potent sodium channel blockers, potent...
2,4(1H)-Diarylimidazoles have been previously shown to inhibit hNaV1.2 sodium (Na) channel currents....
Voltage-gated sodium channels play an integral part in neurotransmission and their dysfunction is fr...
We previously reported that a lipophilic N-(4'-hydroxy-3',5'-di-tert-butylbenzyl) derivative (1) of ...
We have synthesized and evaluated a series of 1,4-disubstituted-triazole derivatives for inhibition ...
Sponges of the genus Agelas produce compounds that modulate the activity of voltage-gated sodium ion...
Voltage-gated sodium channels (VGSC) are responsible for the selective influx of sodium ions in exci...
Voltage-gated sodium channels (VGSC) are responsible for the selective influx of sodium ions in exci...
Drug screening on sodium currents of native myofibers by means of voltage-clamp recordings is predic...
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (NaV) channel...
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na$_V$) chan...
In the present investigation, the rationale for the design, synthesis, and biological evaluation of ...
Previously identified potent and/or use-dependent mexiletine (Mex) analogs were used as template for...