21 results for "Voltage-gated Sodium Channel Blockers" in Products
Voltage-gated Sodium Channel Blockers Products
Voltage-gated sodium channels (NaV) are responsible for action potential initiation and propagation in excitable cells, including nerve, muscle, and neuroendocrine cell types. They are also expressed at low levels in non-excitable cells, where their physiological role is unclear.
Structurally, NaV channels are composed of one pore-forming α-subunit, which may be associated with either one or more β-subunits. α-subunits are composed of four homologous domains, each of which contains six transmembrane segments. The fourth transmembrane loop (S4) acts as the 'voltage sensor' and is activated by changes in membrane potential. S4 is also involved in channel gating.
Na+ channel blocker
| Alternate Names: | TTx |
| Chemical Name: | (4R,4aR,5R,7S,9S,10S,10aR,11S,12S)-Octahydro-12-(hydroxymethyl)-2-imino-5,9:7,10a-dimethano-10aH-[1,3]dioxocino[6,5-d]pyrimidine-4,7,10,11,12-pentol |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker; citrate salt of tetrodotoxin (Cat. No. 1078)
| Alternate Names: | TTx citrate |
| Chemical Name: | (4R,4aR,5R,7S,9S,10S,10aR,11S,12S)-Octahydro-12-(hydroxymethyl)-2-imino-5,9:7,10a-dimethano-10aH-[1,3]dioxocino[6,5-d]pyrimidine-4,7,10,11,12-pentol citrate |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker
| Chemical Name: | N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium chloride |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker
| Chemical Name: | N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium bromide |
| Purity: | ≥98% (HPLC) |
Cardiac Na+ channel blocker. Antiarrhythmic
| Chemical Name: | N-(2-Piperidylmethyl)-2,5-bis-(2,2,2-trifluoroethoxy)benzamide acetate |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker; also I2 imidazoline ligand
| Chemical Name: | 3,5-Diamino-N-(aminoiminomethyl)-6-chloropyrazinecarboxamide hydrochloride |
| Purity: | ≥98% (HPLC) |
Selective NaV1.8 channel blocker
| Chemical Name: | 5-(4-Chlorophenyl)-N-(3,5-dimethoxyphenyl)-2-furancarboxamide |
| Purity: | ≥98% (HPLC) |
Potent and selective NaV1.8 channel blocker; active in vivo
| Chemical Name: | 1-Methyl-1-[4-(4-trifluoromethoxy-phenyl)-1H-imidazol-2-yl]-ethylamine |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker; antiarrhythmic agent
| Alternate Names: | Ko 1173 |
| Chemical Name: | 1-(2,6-Dimethylphenoxy)-2-propanamine hydrochloride |
| Purity: | ≥98% (HPLC) |
Potent and selective Nav1.7 channel blocker
| Chemical Name: | 4-[2-(3-Amino-1H-pyrazol-4-yl)-4-chlorophenoxy]-5-chloro-2-fluoro-N-4-thiazolylbenzenesulfonamide tosylate |
| Purity: | ≥98% (HPLC) |
NaV channel blocker
| Chemical Name: | N-[2-Methyl-3-[[4-[4-[[4-(trifluoromethoxy)phenyl]methoxy]-1-piperidinyl]-1,3,5-triazin-2-yl]amino]phenyl]acetamide |
| Purity: | ≥98% (HPLC) |
Na+ channel blocker
| Chemical Name: | 2-Diethylamino-N-(2,6-dimethylphenyl)acetamide |
| Purity: | ≥98% (HPLC) |
Potent and selective NaV1.3 and NaV1.1 channel blocker
| Chemical Name: | α-Phenyl-N-[4-[(2-thiazolylamino)sulfonyl]phenyl]benzeneacetamide |
| Purity: | ≥98% (HPLC) |
GABA uptake inhibitor; also inhibits glutamate release and blocks NaV channels
| Chemical Name: | 2-Amino-6-trifluoromethoxybenzothiazole hydrochloride |
| Purity: | ≥98% (HPLC) |
Selective NaV1.5 channel blocker
| Purity: | ≥95% (HPLC) |
Potent voltage-dependent NaV1.8 channel blocker
| Chemical Name: | 5-(4-Butoxy-3-chlorophenyl)-N-[[2-(4-morpholinyl)-3-pyridinyl]methyl-3-pyridine carboxamide |
| Purity: | ≥97% (HPLC) |
Selective NaV1.7 channel blocker
| Purity: | ≥95% (HPLC) |
ASIC3 channel blocker
| Purity: | ≥95% (HPLC) |
NaV blocker; neuroprotective
| Alternate Names: | 619C89 |
| Chemical Name: | 2-(4-Methyl-1-piperazinyl)-5-(2,3,5-trichlorophenyl)-4-pyrimidinamine |
| Purity: | ≥98% (HPLC) |
Potent hNav1.4, rNav1.6 and rNav1.7 channel activator
| Purity: | ≥95% (HPLC) |
Potent and selective Nav1.7 blocker; analgesic
| Chemical Name: | 4-[[1-[[2-Chloro-5-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]methoxy]-5-cyclopropyl-2-fluoro-N-(methylsulfonyl)benzamide |
| Purity: | ≥98% (HPLC) |
