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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12951 | Sodium Channel inhibitor 2 | Sodium Channel | |
Sodium Channel inhibitor 2 is a blocker of sodium channel. | |||
T7336 | ICA-121431 | 2,2-Diphenyl-N-[4-(thiazol-2-ylsulfamoyl | Sodium Channel |
ICA-121431 (2,2-Diphenyl-N-[4-(thiazol-2-ylsulfamoyl) is a nanomolar potent small molecule Nav1.7 channel inhibitor with IC50 of 19 nM for rat Nav1.7, with little or no activity against human Nav1.5 or Nav1.7 channels. | |||
T7806 | Licarbazepine | 10,11-hydroxy-10,11 Dihydrocarbamezer | Others |
Licarbazepine (10,11-hydroxy-10,11 Dihydrocarbamezer) is the pharmacologically active metabolite of oxcarbazepine, a drug indicated for the treatment of partial seizures and bipolar disorders. | |||
T7349 | Ralfinamide | Priralfinamide,FCE-26742A | Sodium Channel |
Ralfinamide (Priralfinamide) is an orally available Na-channel blocker for the treatment of neuropathic pain and other pain conditions. | |||
T3285 | Eslicarbazepine Acetate | Zebinix,Aptiom,BIA 2-093,Exalief,Stedesa | Beta-Secretase , Sodium Channel |
Eslicarbazepine Acetate (Zebinix) is an anticonvulsant medication approved for use in Europe, the United States and Canada as an adjunctive therapy for partial-onset seizures that are not adequately controlled with conve... | |||
T8579 | Nav1.8-IN-1 | 5-(4-Chlorophenyl)-N-[[2-(2,2,2-trifluoroethoxy)pyridin-3-yl]methyl]pyridine-3-carboxamide,CHEMBL1270208 | Sodium Channel |
Nav1.8-IN-1 (CHEMBL1270208) is an inhibitor of human NaV1.8 | |||
T2391 | Camostat mesylate | FOY-S980,FOY305,Camostat mesilate | Serine/threonin kinase , SARS-CoV , Sodium Channel |
Camostat mesylate (FOY-S980) is a trypsin-like protease inhibitor and inhibits airway epithelial sodium channel (ENaC) function. | |||
T80533 | Pterinotoxin-2 | Sodium Channel | |
Pterinotoxin-2 is a peptide toxin that acts as a sodium channel inhibitor [1]. | |||
T80451 | Ceratotoxin-2 | CcoTx2,β-TRTX-cm1b | Sodium Channel |
Ceratotoxin-2 (CcoTx2) is a voltage-gated sodium channel inhibitor, demonstrating half maximal inhibitory concentrations (IC50) of 8 nM for Na v 1.2/β 1 and 88 nM for Na v 1.3/β 1 [1]. | |||
T83739 | Myr-Tat-CBD3 TFA | Myr-Tat-Calcium Channel-binding Domain 3,N-myristate-Tat-CBD3 | |
Myr-Tat-CBD3 is a chemical compound that serves as an inhibitor of the protein-protein interaction between the N-type voltage-gated calcium channel Cav2.2 and collapsin response mediator protein 2 (CRMP2). This compound ... | |||
T37847 | Zonisamide-13C2,15N | Zonisamide-13C2,15N | |
Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels ... |