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Home >> Signaling Pathways >> Membrane Transporter/Ion Channel

Membrane Transporter/Ion Channel

Products for  Membrane Transporter/Ion Channel

  1. Cat.No. Product Name Information
  2. GC16823 Enniatin Complex ionophore Enniatin Complex Chemical Structure
  3. GC18105 Enterostatin Enterostatin, human, mouse, rat is a pentapeptide that reduces fat intake. Enterostatin Chemical Structure
  4. GC43623 Erastin2 Erastin2 is a potent system xc- inhibitor and ferroptosis-inducing agent [1]. Erastin2 Chemical Structure
  5. GC13809 Eslicarbazepine acetate antiepileptic drug Eslicarbazepine acetate Chemical Structure
  6. GC48984 Esomeprazole An H+/K+-ATPase inhibitor Esomeprazole Chemical Structure
  7. GC14313 Esomeprazole Magnesium Proton pump inhibitor Esomeprazole Magnesium Chemical Structure
  8. GC36009 Esomeprazole magnesium salt Esomeprazole magnesium salt ((S)-Omeprazole magnesium salt) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole magnesium salt Chemical Structure
  9. GC13022 Esomeprazole Magnesium trihydrate An H+/K+-ATPase inhibitor Esomeprazole Magnesium trihydrate Chemical Structure
  10. GC33575 Esomeprazole potassium salt ((S)-Omeprazole potassium) Esomeprazole potassium salt ((S)-Omeprazole potassium) ((S)-Omeprazole potassium salt) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole potassium salt ((S)-Omeprazole potassium) Chemical Structure
  11. GC10599 Esomeprazole Sodium Proton pump inhibitor Esomeprazole Sodium Chemical Structure
  12. GC48979 Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate) A substrate of multidrug resistance protein 2 Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate) Chemical Structure
  13. GC10964 Estradiol 17-(β-D-Glucuronide) (sodium salt) Estradiol 17-(β-D-Glucuronide) sodium, a metabolite of estrogen, is well known to cause intrahepatic cholestasis in humans. Estradiol 17-(β-D-Glucuronide) (sodium salt) Chemical Structure
  14. GC17065 Estradiol 3-(β-D-Glucuronide) (sodium salt) substrate for multidrug resistance protein 2 (MRP2) Estradiol 3-(β-D-Glucuronide) (sodium salt) Chemical Structure
  15. GC64673 Etbicyphat Etbicyphat (Trimethylopropane phosphate) is a potent GABA(A) receptors competitive antagonist. Etbicyphat Chemical Structure
  16. GC25386 Ethacrynate Sodium Ethacrynate Sodium (ethacrynic acid sodium) is the sodium salt form of ethacrynic acid, which inhibits symport of sodium, potassium, and chloride primarily in the ascending limb of Henle, but also in the proximal and distal tubules. Ethacrynate Sodium Chemical Structure
  17. GC14041 Ethacrynic Acid Na+/K+/2Cl- cotransporter NKCC2 inhibitor Ethacrynic Acid Chemical Structure
  18. GC10519 Ethacrynic acid - d5 Used as an internal standard for GC- or LC-mass spectrometry Ethacrynic acid - d5 Chemical Structure
  19. GC33695 Ethosuximide An anticonvulsant Ethosuximide Chemical Structure
  20. GC15824 Ethyl 3-Aminobenzoate (methanesulfonate) Ethyl 3-Aminobenzoate (methanesulfonate) (MS-222) is common used to immobilize fish for marking or transport and to suppress sensory systems during invasive procedures. Ethyl 3-Aminobenzoate (methanesulfonate) Chemical Structure
  21. GC31023 Ethyl dirazepate Ethyl dirazepate is a drug which is a benzodiazepine derivative. Ethyl dirazepate Chemical Structure
  22. GC36012 Etifoxine A positive allosteric modulator of GABAA receptors Etifoxine Chemical Structure
  23. GC33700 Etiracetam (UCB 6474) Etiracetam (UCB 6474) (UCB 6474) is an acetylcholine agonist and a nootropic drug of the racetam family. Etiracetam (UCB 6474) Chemical Structure
  24. GC16134 Etomidate

    General anesthetic with GABA modulatory and GABA-mimetic actions

     Etomidate Chemical Structure
  25. GC16985 Etomidate hydrochloride

    GABAA receptors agonist

     Etomidate hydrochloride Chemical Structure
  26. GC65248 Etripamil Etripamil (MSP-2017) is a short-acting L-type calcium-channel antagonist, can be used for the research of Paroxysmal Supraventricular Tachycardia (PSVT). Etripamil Chemical Structure
  27. GC30910 Eucalyptol (1,8-Cineole) A bicyclic monoterpene with diverse biological activities Eucalyptol (1,8-Cineole) Chemical Structure
  28. GC13947 Evans Blue tetrasodium salt Evans Blue tetrasodium salt is a potent inhibitor of L-glutamate uptake via the membrane bound excitatory amino acid transporter (EAAT). Evans Blue tetrasodium salt Chemical Structure
  29. GC38389 Evenamide Evenamide (NW-3509) is an orally available voltage-gated sodium channel (VGSC) blocker (Ki=0.4 ?M) for the research of schizophrenia. Evenamide Chemical Structure
  30. GC66016 Evifacotrep Evifacotrep, a short transient receptor potential channel 5 (TRPC5) antagonist (WO2020061162, compound 100), can be used for the research of neurological diseases. Evifacotrep Chemical Structure
  31. GC25405 Evodine Evodine, a natural product extracted from Evodiae fructus (EF), is a biomarker for quality assessment of EF in the Chinese Pharmacopoeia. Evodine is a potent P-gp inhibitor. Evodine Chemical Structure
  32. GC15941 EVP-6124 A partial agonist of α7 subunit-containing nAChRs EVP-6124 Chemical Structure
  33. GC11091 EVP-6124 hydrochloride A partial agonist of α7 subunit-containing nAChRs EVP-6124 hydrochloride Chemical Structure
  34. GC67895 EVT-401 EVT-401 Chemical Structure
  35. GC39748 Facinicline hydrochloride Facinicline hydrochloride (RG3487 hydrochloride) is an orally active nicotinic α7 receptor partial agonist, with a Ki of 6 nM for α7 human nAChR. Facinicline hydrochloride Chemical Structure
  36. GC36027 Fanapanel hydrate Fanapanel hydrate (ZK200775 hydrate) is a highly selective AMPA/kainate antagonist with little activity against NMDA; have Ki values of 3.2 nM, 100 nM, and 8.5 μM against quisqualate, kainate, and NMDA, respectively. Fanapanel hydrate Chemical Structure
  37. GC19152 Fantofarone Fantofarone is a highly potent Calcium Channel antagonist. Fantofarone Chemical Structure
  38. GC18223 Farampator Farampator is a positive allosteric modulator of AMPA receptors that has an EC50 value greater than 32 uM for evoking glutamate currents in isolated pyramidal neurons. Farampator Chemical Structure
  39. GC43654 Fasentin Fasentin is an inhibitor of glucose transport. Fasentin Chemical Structure
  40. GC13869 Fasudil Calcium antagonist Fasudil Chemical Structure
  41. GC14289 Fasudil (HA-1077) HCl Fasudil (HA-1077; AT877) Hydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil (HA-1077) HCl is also a potent Ca2+ channel antagonist and vasodilator. Fasudil (HA-1077) HCl Chemical Structure
  42. GC36034 FD 12-9 FD 12-9 is a flavonoid dimer, acts as a dual inhibitor of P-gp and BCRP, with EC50s of 285 nM and 0.9 nM, respectively. Anti-glioblastoma activity. FD 12-9 Chemical Structure
  43. GC10522 Felbamate antagonist at the NMDA-associated glycine binding site Felbamate Chemical Structure
  44. GC15363 Felbamate hydrate N-methyl-D-aspartate (NMDA) inhibitor Felbamate hydrate Chemical Structure
  45. GC17173 Felodipine Selective L-type Ca2+ channel blocker Felodipine Chemical Structure
  46. GC66436 FEMA 4809 FEMA 4809 is a TRPM8 receptor agonist (EC50=0.2 nM) for use as a cooling agent. TRPM8 is the ion channel responsible for the cool perception. FEMA 4809 Chemical Structure
  47. GC60834 Fenamic acid Fenamic acid (N-Phenylanthranilic acid, NPAA) is an orally active chloride channel blocker. Fenamic acid Chemical Structure
  48. GC18086 Fendiline (hydrochloride) α2-adrenergic receptor antagonist Fendiline (hydrochloride) Chemical Structure
  49. GC47338 Fenoxycarb A non-neurotoxic carbamate insecticide Fenoxycarb Chemical Structure
  50. GC49278 Fenpropathrin A pyrethroid insecticide Fenpropathrin Chemical Structure
  51. GC60165 Ferulamide Ferulamide is a Ferulic acid derivative isolated from Portulaca oleracea L. Ferulamide Chemical Structure
  52. GC18641 Ferutinin Ferutinin is a plant-derived ester of a sesquiterpenic alcohol that acts as an agonist for estrogen receptor (ER) α (IC50 = 33.1 nM) and an agonist/antagonist for ERβ (IC50 = 180.5 nM). Ferutinin Chemical Structure
  53. GC50649 FFN 200 dihydrochloride FFN 200 dihydrochloride Chemical Structure
  54. GC12568 FG 7142 benzodiazepine inverse agonist and anxiogenic agent FG 7142 Chemical Structure
  55. GC33754 FG8119 (NNC13-8119) FG8119 (NNC13-8119) is a novel benzodiazepine agonist extracted from patent US 4745112 A. FG8119 (NNC13-8119) Chemical Structure
  56. GC14017 FGIN-1-27

    high affinity agonist of the translocator protein (TSPO,peripheral benzodiazepine receptor)

     FGIN-1-27 Chemical Structure
  57. GC16238 FGIN-1-43 ligand as probe for the mitochondial DBI receptor (peripheral benzodiazepine receptor) FGIN-1-43 Chemical Structure
  58. GC63444 Filapixant Filapixant is a purinoreceptor antagonist extracted from patent WO2016091776A1, example 348. Filapixant Chemical Structure
  59. GC47352 FK-506-13C-d2 An internal standard for the quantification of FK-506 FK-506-13C-d2 Chemical Structure
  60. GC49102 Flavoxate-d5 An internal standard for the quantification of flavoxate Flavoxate-d5 Chemical Structure
  61. GC65416 Flecainide Flecainide is a potent and orally active antiarrhythmic agent. Flecainide Chemical Structure
  62. GC15823 Flecainide acetate An inhibitor of cardiac late sodium current Flecainide acetate Chemical Structure
  63. GC65150 Flecainide hydrochloride Flecainide hydrochloride is a potent and orally active antiarrhythmic agent. Flecainide hydrochloride Chemical Structure
  64. GC47354 Flonicamid A pyridinecarboxamide insecticide Flonicamid Chemical Structure
  65. GC13466 Flufenamic acid

    TRPC activator

     Flufenamic acid Chemical Structure
  66. GC10772 Flumazenil

    Benzodiazepine antagonist

     Flumazenil Chemical Structure
  67. GC36058 Flumazenil acid Flumazenil acid is a metabolite of Flumazenil. Flumazenil acid Chemical Structure
  68. GC16532 Flunarizine 2HCl Flunarizine 2HCl is a potent dual Na+/Ca2+ channel (T-type) blocker. Flunarizine 2HCl Chemical Structure
  69. GC49739 Fluo-2 (potassium salt) A cell-impermeable fluorescent calcium indicator Fluo-2 (potassium salt) Chemical Structure
  70. GC49458 Fluo-2 AM A cell-permeable fluorescent calcium indicator Fluo-2 AM Chemical Structure
  71. GC43681 Fluo-3 (ammonium salt)

    Fluo-3 (ammonium salt) is a fluorescent calcium indicator commonly used in flow cytometry and cell-based experiments to detect changes in intracellular calcium levels.

     Fluo-3 (ammonium salt) Chemical Structure
  72. GC43682 Fluo-3 (potassium salt) Fluo-3 (potassium salt) is a fluorescent calcium indicator commonly used in flow cytometry and cell-based experiments to detect changes in intracellular calcium levels. Fluo-3 (potassium salt) Chemical Structure
  73. GC43683 Fluo-3 (sodium salt) Fluo-3 is a fluorescent calcium indicator commonly used in flow cytometry and cell-based experiments to detect changes in intracellular calcium levels. Fluo-3 (sodium salt) Chemical Structure
  74. GC43684 Fluo-3FF (potassium salt) Fluo-3FF is a fluorescent calcium indicator. Fluo-3FF (potassium salt) Chemical Structure
  75. GC49741 Fluo-4 (potassium salt) A cell-impermeable fluorescent calcium indicator Fluo-4 (potassium salt) Chemical Structure
  76. GC36060 Flupirtine Flupirtine(D 9998) is a selective neuronal potassium channel opener that also has NMDA receptor antagonist properties. Flupirtine Chemical Structure
  77. GC11470 Flupirtine maleate NMDA receptor antagonist Flupirtine maleate Chemical Structure
  78. GC66073 Flupyradifurone Flupyradifurone is a systemic nAChR agonist that interferes with signal transduction in the central nervous system of sucking pests. Flupyradifurone can be used as a butenolide insecticide. Flupyradifurone Chemical Structure
  79. GC64394 Flupyrimin Flupyrimin acts as an antagonist at the insect nicotinic acetylcholine receptor (nAChR). Flupyrimin Chemical Structure
  80. GC11492 Fluspirilene potent, non-competitive antagonist of agonist-activated L-type calcium channels Fluspirilene Chemical Structure
  81. GC49397 Fluvoxamine-d4 (maleate) An internal standard for the quantification of fluvoxamine Fluvoxamine-d4 (maleate) Chemical Structure
  82. GC30088 Fluxametamide Fluxametamide is an insecticide with wide spectrum, acts as an antagonist of GABA- and glutamate-gated chloride channels, with IC50 of 1.95 nM and 225 nM for M. Fluxametamide Chemical Structure
  83. GC10506 FPL 64176 L-type Ca2+ channels activator FPL 64176 Chemical Structure
  84. GC33895 FR183998 free base FR183998 free base is a potent Na+/H+-exchange inhibitor, with IC50s of 0.3 nM, 3.1 nM and 6.5 nM by measurement of pHi change in rat lymphocytes, rat and human platelets, respectively. FR183998 free base Chemical Structure
  85. GC49089 FR900359

    A cyclic depsipeptide and an inhibitor of Gαq, Gα11, and Gα14

     FR900359 Chemical Structure
  86. GC18260 FTase Inhibitor I FTase inhibitor I is a potent inhibitor of farnesyltransferase (FTase; IC50 = 21 nM) that is greater than 30-fold selective for FTase over geranylgeranyl transferase (GGTase; IC50 = 790 nM). FTase Inhibitor I Chemical Structure
  87. GC52503 FTase Inhibitor II (trifluoroacetate salt) A potent, selective inhibitor of farnesyltransferase FTase Inhibitor II (trifluoroacetate salt) Chemical Structure
  88. GC10874 Fumitremorgin C multidrug transporter inhibitor Fumitremorgin C Chemical Structure
  89. GC30628 Funapide (TV 45070) Funapide (TV 45070) (TV 45070; XEN402) is a potent Sodium Channel Nav1.7 inhibitor. Funapide (TV 45070) Chemical Structure
  90. GC43711 Fura-2 (potassium salt) Fura-2 (potassium salt) is a scaled fluorescent dye that can be used for intracellular calcium imaging with the Kd value of 140 nM. Fura-2 (potassium salt) Chemical Structure
  91. GC43712 Fura-2 (sodium salt) Fura-2 is a ratiometric fluorescent calcium indicator that can be used to detect calcium in cells. Fura-2 (sodium salt) Chemical Structure
  92. GC49462 Fura-2 Leakage Resistant (potassium salt) A cell-impermeable, ratiometric fluorescent calcium indicator Fura-2 Leakage Resistant (potassium salt) Chemical Structure
  93. GC49465 Fura-2 Leakage Resistant AM A cell-permeable, ratiometric fluorescent calcium indicator Fura-2 Leakage Resistant AM Chemical Structure
  94. GC43713 Fura-FF (potassium salt) Fura-FF (potassium salt) is a low-affinity fluorescent dye for calcium (Ex/Em: 365/514 nm in the absence of calcium; 339/507 nm in the presence of a high calcium concentration). Fura-FF (potassium salt) Chemical Structure
  95. GC43714 Fura-FF AM Fura-FF AM is a cell-permeable acetoxymethyl ester of the fluorescence calcium indicator fura-FF (potassium salt). Fura-FF AM Chemical Structure
  96. GC12970 Furosemide GABAA receptors antagonist Furosemide Chemical Structure
  97. GC36091 Furosemide sodium A loop diuretic inhibitor of Na+/2Cl-/K+ (NKCC) cotransporter Furosemide sodium Chemical Structure
  98. GC12714 Gabapentin

    GABA enhancer

     Gabapentin Chemical Structure
  99. GC36097 Gabapentin enacarbil Gabapentin enacarbil (XP-13512) is a prodrug for the anticonvulsant and analgesic drug gabapentin. Gabapentin enacarbil Chemical Structure
  100. GC17316 Gabapentin HCl Gabapentin HCl is a potent, orally active P/Q type Ca2+ channel blocker. Gabapentin HCl Chemical Structure
  101. GC38543 Gaboxadol hydrochloride A GABAA receptor agonist and GABAC receptor antagonist Gaboxadol hydrochloride Chemical Structure

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