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Sodium Channel

Sodium channel are integral membrane proteins that form ion channels, conducting sodium ions (Na+) through a cell plasma membrane.

Products for  Sodium Channel

  1. Cat.No. Product Name Information
  2. GC45985 (±)-Indoxacarb (±)-Indoxacarb  Chemical Structure
  3. GC30933 (+)-Kavain (+)-Kavain  Chemical Structure
  4. GC34952 (-)-Sparteine sulfate pentahydrate (-)-Sparteine sulfate pentahydrate  Chemical Structure
  5. GC62739 (R)-Funapide (R)-Funapide  Chemical Structure
  6. GC42327 4,9-Anhydrotetrodotoxin

    4,9-Anhydrotetrodotoxin (4,9-anhydro-TTX) is a derivative of TTX that selectively blocks inward sodium current through Nav1.6 voltage-activated sodium channels (IC50 = 7.8 nM in Xenopus oocytes).

    4,9-Anhydrotetrodotoxin  Chemical Structure
  7. GC35147 5-(N,N-Hexamethylene)-amiloride 5-(N,N-Hexamethylene)-amiloride  Chemical Structure
  8. GC14481 A 887826 voltage-dependent Nav1.8 sodium channel blocker A 887826  Chemical Structure
  9. GC15701 A-803467 NaV1.8 channel blocker,potent and selective A-803467  Chemical Structure
  10. GC35273 Ajmaline Ajmaline  Chemical Structure
  11. GC30917 AM-2099 AM-2099  Chemical Structure
  12. GC15458 Ambroxol HCl TTX-resistant Na+ currents inhibitor Ambroxol HCl  Chemical Structure
  13. GC31431 Amiloride (MK-870) Amiloride (MK-870)  Chemical Structure
  14. GC17853 Amiloride HCl epithelial sodium channel (ENaC) inhibitor, selective Amiloride HCl  Chemical Structure
  15. GC12051 Amiloride HCl dihydrate potent epithelial sodium channel (ENaC) blocker Amiloride HCl dihydrate  Chemical Structure
  16. GC13723 Amitriptyline HCl Serotonin /norepinephrine receptor/5-HT4/5-HT2 inhibitor Amitriptyline HCl  Chemical Structure
  17. GC18203 Annonacin Annonacin is a potent and lipophilic acetogenin from A. Annonacin  Chemical Structure
  18. GC63799 AZ194 AZ194  Chemical Structure
  19. GC11693 Benzamil hydrochloride

    Na+/Ca2+ exhanger (NCX) inhibitor

    Benzamil hydrochloride  Chemical Structure
  20. GC13125 Benzocaine Sodium channel inhibitor Benzocaine  Chemical Structure
  21. GC34486 BI 01383298 BI 01383298  Chemical Structure
  22. GC34492 BI-9627 BI-9627  Chemical Structure
  23. GC60642 Bifenthrin Bifenthrin  Chemical Structure
  24. GC64658 Bliretrigine Bliretrigine  Chemical Structure
  25. GC42976 Brevetoxin B Brevetoxin B is a polyketide neurotoxin produced by Karenia species and other dinoflagellates. Brevetoxin B  Chemical Structure
  26. GC35568 Bulleyaconitine A Bulleyaconitine A  Chemical Structure
  27. GC12410 Bupivacaine HCl Anaesthetic drug Bupivacaine HCl  Chemical Structure
  28. GC17340 Carbamazepine Inhibitor of neuronal voltage-gated Na+ channels Carbamazepine  Chemical Structure
  29. GC17842 CARIPORIDE Potent NHE inhibitor CARIPORIDE  Chemical Structure
  30. GC30798 Cenobamate (YKP3089) Cenobamate (YKP3089)  Chemical Structure
  31. GC30280 Chlorpromazine D6 hydrochloride Chlorpromazine D6 hydrochloride  Chemical Structure
  32. GC14216 Chlorpromazine HCl

    dopamine receptor antagonist

    Chlorpromazine HCl  Chemical Structure
  33. GC16182 Co 102862 voltage-gated sodium channel blocker Co 102862  Chemical Structure
  34. GC15915 Dibucaine Local anesthetic Dibucaine  Chemical Structure
  35. GC16696 Dibucaine (Cinchocaine) HCl Sodium channel inhibitor Dibucaine (Cinchocaine) HCl  Chemical Structure
  36. GC35860 Dibucaine hydrochloride Dibucaine hydrochloride  Chemical Structure
  37. GC38484 Dimethyl lithospermate B Dimethyl lithospermate B  Chemical Structure
  38. GC43478 Disopyramide Disopyramide is a sodium channel blocker that, in rabbit ventricular myocytes, binds and dissociates from open channels more quickly than from resting channels. Disopyramide  Chemical Structure
  39. GC35903 DSP-2230 DSP-2230  Chemical Structure
  40. GC15893 EIPA

    TRPP3 channel inhibitor

    EIPA  Chemical Structure
  41. GC35970 EIPA hydrochloride EIPA hydrochloride  Chemical Structure
  42. GC30063 Eleclazine hydrochloride (GS 6615 hydrochloride) Eleclazine hydrochloride (GS 6615 hydrochloride)  Chemical Structure
  43. GC35993 Eniporide hydrochloride Eniporide hydrochloride  Chemical Structure
  44. GC13809 Eslicarbazepine acetate antiepileptic drug Eslicarbazepine acetate  Chemical Structure
  45. GC15824 Ethyl 3-Aminobenzoate (methanesulfonate) block the generation of action potentials through voltage-dependent Na+-channels Ethyl 3-Aminobenzoate (methanesulfonate)  Chemical Structure
  46. GC38389 Evenamide Evenamide  Chemical Structure
  47. GC15823 Flecainide acetate Antiarrhythmic drug Flecainide acetate  Chemical Structure
  48. GC33895 FR183998 free base FR183998 free base  Chemical Structure
  49. GC30628 Funapide (TV 45070) Funapide (TV 45070)  Chemical Structure
  50. GC64206 GDC-0310 GDC-0310  Chemical Structure
  51. GN10799 Ginsenoside Rg3 Ginsenoside Rg3 affects endothelium dependent relaxation in the aorta. Ginsenoside Rg3  Chemical Structure
  52. GC31065 GNE-131 GNE-131  Chemical Structure
  53. GC10830 GS967 inhibitor of cardiac late sodium current GS967  Chemical Structure
  54. GC10234 GSK1014802(CNV1014802) Novel sodium channel blocker GSK1014802(CNV1014802)  Chemical Structure
  55. GC50707 GX 201 GX 201  Chemical Structure
  56. GC39792 Halazone Halazone  Chemical Structure
  57. GC12806 Huwentoxin IV NaV1.7 channel blocker Huwentoxin IV  Chemical Structure
  58. GC15860 Ibutilide Fumarate Class III antiarrhythmic agent Ibutilide Fumarate  Chemical Structure
  59. GC17395 ICA 121431 human NaV1.3 and NaV1.1 channels inhibitor ICA 121431  Chemical Structure
  60. GC10836 Jingzhaotoxin III NaV1.5 channels blocker Jingzhaotoxin III  Chemical Structure
  61. GC16786 KC 12291 hydrochloride voltage-gated sodium channel blocker KC 12291 hydrochloride  Chemical Structure
  62. GC14764 Lamotrigine 5-HT inhibitor, sodium channel blocker Lamotrigine  Chemical Structure
  63. GC64113 Lamotrigine-13C3,d3 Lamotrigine-13C3,d3  Chemical Structure
  64. GC15978 Levobupivacaine HCl Sodium channel inhibitor Levobupivacaine HCl  Chemical Structure
  65. GC13505 Licarbazepine voltage-gated sodium channel blocker Licarbazepine  Chemical Structure
  66. GC17608 Lidocaine Anasthetic and class Ib antiarrhythmic agent Lidocaine  Chemical Structure
  67. GC33831 Lidocaine hydrochloride (Lignocaine hydrochloride) Lidocaine hydrochloride (Lignocaine hydrochloride)  Chemical Structure
  68. GC61594 Lu AE98134 Lu AE98134  Chemical Structure
  69. GC63063 Mebeverine hydrochloride Mebeverine hydrochloride  Chemical Structure
  70. GC41540 Mepivacaine Mepivacaine is an analytical reference standard that is categorized as an anesthetic. Mepivacaine  Chemical Structure
  71. GC10224 Mepivacaine HCl

    local anesthetic

    Mepivacaine HCl  Chemical Structure
  72. GC34665 Metaflumizone Metaflumizone  Chemical Structure
  73. GC61046 Methocarbamol D5 Methocarbamol D5  Chemical Structure
  74. GC11069 Meticrane Peripheral-type benzodiazepine receptor (PBR) inhibitor Meticrane  Chemical Structure
  75. GC44189 Mexiletine (hydrochloride) Mexiletine is a voltage-gated sodium channel blocker and class Ib antiarrhythmic agent that preferentially binds to open/inactive channels. Mexiletine (hydrochloride)  Chemical Structure
  76. GC39618 Mexiletine D6 hydrochloride Mexiletine D6 hydrochloride  Chemical Structure
  77. GC36648 Moricizine Moricizine  Chemical Structure
  78. GC31200 Myomodulin Myomodulin  Chemical Structure
  79. GC50071 NAV 26 Selective Nav1.7 channel blocker NAV 26  Chemical Structure
  80. GC61110 Nav1.1 activator 1 Nav1.1 activator 1  Chemical Structure
  81. GC36697 Nav1.7 inhibitor Nav1.7 inhibitor  Chemical Structure
  82. GC36698 NaV1.7 inhibitor-1 NaV1.7 inhibitor-1  Chemical Structure
  83. GC31002 Nav1.7-IN-2 Nav1.7-IN-2  Chemical Structure
  84. GC64072 NBI-921352 NBI-921352  Chemical Structure
  85. GC31302 NHE3-IN-1 NHE3-IN-1  Chemical Structure
  86. GC63108 NHE3-IN-2 NHE3-IN-2  Chemical Structure
  87. GC31216 Nicainoprol (RU-42924) Nicainoprol (RU-42924)  Chemical Structure
  88. GC39719 Nigericin

    K+/H+ ionophore,promoting K+/H+ exchange across mitochondrial membrane

    Nigericin  Chemical Structure
  89. GC50299 OD1 Potent hNav1.4, rNav1.6 and rNav1.7 channel activator OD1  Chemical Structure
  90. GC10500 Oxcarbazepine BTX inhibitor Oxcarbazepine  Chemical Structure
  91. GC11271 Oxybuprocaine HCl Local anesthetic Oxybuprocaine HCl  Chemical Structure
  92. GC31206 PF 04531083 PF 04531083  Chemical Structure
  93. GC12109 PF 04885614 NaV1.8 inhibitor PF 04885614  Chemical Structure
  94. GC36877 PF 05089771 PF 05089771  Chemical Structure
  95. GC19281 PF-01247324 PF-01247324 is a selective and orally bioavailable Nav1.8 channel blocker with an IC50 of 196 nM for recombinant human Nav1.8 channel. PF-01247324  Chemical Structure
  96. GC18947 PF-05089771 (tosylate) PF-05089771 is a voltage-gated sodium channel 1.7 (Nav1.7) blocker (IC50s = 11, 16, 33, and 20 nM for 5N11S, 5A11L, 5A11S, and 5A11L Nav1.7 splice variants, respectively). PF-05089771 (tosylate)  Chemical Structure
  97. GC30322 PF-05241328 PF-05241328  Chemical Structure
  98. GC31095 PF-06305591 PF-06305591  Chemical Structure
  99. GC61175 PF-06305591 dihydrate PF-06305591 dihydrate  Chemical Structure
  100. GC19289 PF-06869206 PF-06869206 is an orally bioavailable selective inhibitor of the sodium-phosphate cotransporter NaPi2a (SLC34A1) with an IC50 of 380 nM. PF-06869206  Chemical Structure
  101. GC16086 Phenytoin inactive voltage-gated sodium channel stabilizer Phenytoin  Chemical Structure

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