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Membrane Transporter/Ion Channel

Ion channels are pore-forming membrane proteins whose functions include establishing a resting membrane potential, shaping action potentials and other electrical signals by gating the flow of ions across the cell membrane, controlling the flow of ions across secretory and epithelial cells, and regulating cell volume. Ion channels are present in the membranes of all cells. Ion channels are one of the two classes of ionophoric proteins, along with ion transporters (including the sodium-potassium pump, sodium-calcium exchanger, and sodium-glucose transport proteins)

Products for Membrane Transporter/Ion Channel

  1. Cat.No. Product Name Information
  2. BCC3760 Dibucaine (Cinchocaine) HCl Dibucaine hydrochloride (Cinchocaine hydrochloride) is a sodium channel inhibitor. Dibucaine hydrochloride is a potent SChE inhibitor. Dibucaine (Cinchocaine) HCl
  3. BCC7373 TNP-ATP triethylammonium salt TNP-ATP triethylammonium salt
  4. BCC5492 Procainamide HCl Procainamide hydrochloride is an anti-arrhythmic agent and is used to treat cardiac arrhythmia; induces rapid block of the batrachotoxin(BTX)-activated sodium channels of the heart muscle and acts as antagonist to long gating closures. Procainamide HCl
  5. BCC6811 DHBP dibromide DHBP dibromide is an inhibitor for calcium release and a muscle relaxant. DHBP dibromide
  6. BCC5814 OMDM-2 OMDM-2 is a potent, selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 3.0 μM. OMDM-2
  7. BCC6621 W-5 hydrochloride W-5 hydrochloride
  8. BCC6622 W-7 hydrochloride W-7 hydrochloride
  9. BCC1986 Tariquidar methanesulfonate, hydrate Tariquidar methanesulfonate, hydrate (XR9576 methanesulfonate, hydrate) is a potent and specific inhibitor of P-glycoprotein (P-gp) with a Kd of 5.1 nM. Tariquidar methanesulfonate, hydrate
  10. BCC7043 NF 449 Highly selective P2X1 antagonist NF 449
  11. BCC6169 TP 003 TP 003
  12. BCC5069 Ouabain Ouabain is a selective Na+/K+, -ATPase inhibitor, binds to α2 /α3 subunit with Ki of 41 nM/15 nM. Ouabain
  13. BCC5071 Phenytoin sodium Phenytoin sodium is an inactive voltage-gated sodium channel stabilizer. Phenytoin sodium
  14. BCC6804 (±)-threo-3-Methylglutamic acid (±)-threo-3-Methylglutamic acid
  15. BCC8024 Rose Bengal Potent VGlut and VMAT inhibitor; cell permeable Rose Bengal
  16. BCC7140 8-CPT-2Me-cAMP, sodium salt Selective Epac activator 8-CPT-2Me-cAMP, sodium salt
  17. BCC4809 Nisoldipine Nisoldipine(BAY-k 5552; Sular) is a calcium channel blocker belonging to the dihydropyridines class, specific for L-type Cav1.2 with IC50 of 10 nM. Nisoldipine
  18. BCC4123 (R)-Baclofen hydrochloride (R)-Baclofen hydrochloride (STX 209 hydrochloride) is a selective GABAB receptor agonist. (R)-Baclofen hydrochloride
  19. BCC5001 Tolbutamide Tolbutamide is a first generation potassium channel blocker, sulfonylurea oral hypoglycemic drug. Tolbutamide
  20. BCC7234 Ro 04-5595 hydrochloride Ro 04-5595 hydrochloride
  21. BCC6595 L-trans-2,4-PDC L-trans-2,4-PDC
  22. BCC5004 Nicorandil Nicorandil (SG-75) is potassium channel activator. Nicorandil
  23. BCC1052 AMG-517 AMG 517 is a potent and selective vanilloid receptor-1 (TRPV1) antagonist with an IC50 of 0.5 nM. AMG-517
  24. BCC7914 GW 542573X GW 542573X
  25. BCC7162 CL 218872 CL 218872
  26. BCC7391 Talniflumate Talniflumate
  27. BCC6952 Thapsigargin Thapsigargin is an inhibitor of microsomal Ca2+-ATPase. Thapsigargin is a well characterized Endoplasmic Reticulum (ER) stress inducing agent. Thapsigargin
  28. BCC7597 Polygodial Polygodial
  29. BCC7864 Bepridil hydrochloride Bepridil hydrochloride (CERM 1978) is a calcium channel blocker, with antianginal activity. Bepridil hydrochloride
  30. BCC2512 Zonisamide Zonisamide is a 1,2 benzisoxazole derivative and the first agent of this chemical class to be developed as an antiepileptic drug. Zonisamide
  31. BCC4240 Zonisamide sodium Zonisamide sodium is a 1,2 benzisoxazole derivative and the first agent of this chemical class to be developed as an antiepileptic drug. Zonisamide sodium
  32. BCC7388 Nonactin Nonactin is a naturally occurring macrotetrolide antibiotic from Streptomyces griseus. Nonactin acts as an ionophore for monovalent cations, including K+, and NH4+. Nonactin is able to uncouple the oxidative phosphorylation of mitochondria. Nonactin selectively induces apoptosis in cell lines harboring active mutant β-catenin. Nonactin inhibits the surface expression of endogenous HSP60. Nonactin
  33. BCC5918 PPDA PPDA
  34. BCC7543 WS 12 WS-12 is an agonist of TRPM8 with an EC50 of 39 nM. WS 12
  35. BCC2039 Vigabatrin Vigabatrin(γ-Vinyl-GABA; Sabril) is a structural analog of the inhibitory neurotransmitter γ-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase. Vigabatrin
  36. BCC6575 Isoguvacine hydrochloride Isoguvacine hydrochloride is a GABA receptor agonist. Isoguvacine hydrochloride
  37. BCC4503 (R)-baclofen (R)-Baclofen(STX209) is a selective GABAB receptor agonist. (R)-baclofen
  38. BCC7452 17-PA 17-PA
  39. BCC6623 W-9 hydrochloride W-9 hydrochloride
  40. BCC6111 TCN 237 dihydrochloride NMDA-IN-1 is a potent and NR2B-selective NMDA antagonist with Ki of 0.85 nM; NR2B Ca2+ influx IC50 is 9.7 nM; no activities on NR2A, NR2C, NR2D, hERG-channel and α1-adrenergic receptor. TCN 237 dihydrochloride
  41. BCC1251 Ivermectin Ivermectin (MK-933) is a broad-spectrum anti-parasite medication used in humans most commonly to treat nematode infections such as onchocerciasis, as well as scabies and lice. Ivermectin (MK-933) is a specific inhibitor of Impα/β1-mediated nuclear import and has potent antiviral activity towards both HIV-1 and dengue virus. It is a positive allosteric effector of P2X4 and the α7 neuronal nicotinic acetylcholine receptor (nAChRs). Ivermectin also inhibits bovine herpesvirus1 (BoHV-1) replication and inhibits BoHV-1 DNA polymerase nuclear import. Ivermectin
  42. BCC1288 (+)-MK 801 (+)-MK 801
  43. BCC7515 Veratridine Veratridine (3-Veratroylveracevine), a alkaloid derived from plants in the family Liliaceae, is a sodium channel agonist. Veratridine inhibits the peak current of Nav1.7, with an IC50 of 18.39 µM. Veratridine
  44. BCC6294 APETx2 APETx2
  45. BCC6629 3-Methyl-GABA 3-Methyl-GABA
  46. BCC7845 Org 24598 lithium salt Org 24598 lithium salt
  47. BCC6867 9-AC 9-AC
  48. BCC4219 Aniracetam Aniracetam(Ro 13-5057) is a nootropics and neuroprotective drug, which is selectively modulates the AMPA receptor and nAChR. Aniracetam
  49. BCC7927 Psora 4 Potent KV1.3 channel blocker Psora 4
  50. BCC7938 STF 31 STF-31 is an inhibitor of glucose transporter 1 (GLUT1, IC50 = 1 μM). STF 31
  51. BCC4402 Felodipine Felodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. Felodipine
  52. BCC7760 K858 K858 Racemic is an ATP-uncompetitive inhibitor of kinesin Eg5 with an IC50 of 1.3 μM. K858
  53. BCC6565 L-(-)-threo-3-Hydroxyaspartic acid L-(-)-threo-3-Hydroxyaspartic acid
  54. BCC7526 CyPPA CyPPA
  55. BCC5692 SCH 50911 SCH 50911, (+)-(S)-5,5-dimethylmorpholinyl-2-acetic acid, a selective, orally-active and competitive γ-Aminobutyric acid B GABA(B) receptor antagonist, binds to GABA(B) receptor with IC50 of 1.1 μM. SCH 50911 antagonizes GABA(B) autoreceptors, increasing the electrically-stimulated 3H overflow with an IC50 of 3 μM. SCH 50911
  56. BCC6587 cis-ACBD cis-ACBD
  57. BCC6555 (-)-Bicuculline methobromide (-)-Bicuculline methobromide (l-Bicuculline methobromide) is a potent GABAA receptor antagonist. (-)-Bicuculline methobromide blocks afterhyperpolarizations (AHPs) mediated by Ca2+-activated K+ channels in various types of neurons. (-)-Bicuculline methobromide
  58. BCC6560 (RS)-AMPA (RS)-AMPA
  59. BCC2037 Vernakalant Hydrochloride Vernakalant hydrochloride is a mixed voltage- and frequency-dependent Na+ and atria-preferred K+ channel blocker. IC50 for block by Vernakalant of wild-type and mutant Kv1.5 channels Fractional block is 13.35±0.93 μM, 0.61±0.03 μM, and 1.63±0.09 μM for Kv1.5 channelwt, Kv1.5 channelI508F, Kv1.5 channelT479A, respectively. Vernakalant Hydrochloride
  60. BCC6943 CGP 37157 CGP37157 is a potent, selective inhibitor of Na+/Ca2+ exchanger, inhibiting the Na+-induced Ca2+-release from guinea-pig heart mitochondria, with an IC50 of 0.8 μM. CGP 37157
  61. BCC4456 Flupirtine maleate Flupirtine Maleate(D 9998) is a selective neuronal potassium channel opener that also has NMDA receptor antagonist properties. Flupirtine maleate
  62. BCC3799 Nilvadipine Nilvadipine is a potent calcium channel antagonist, and the IC50 value is around 0.1 nM. Nilvadipine
  63. BCC3797 Isradipine (Dynacirc) Isradipine(Dynacirc) is a calcium channel blocker with an IC50 of 34±8 μM. Isradipine (Dynacirc)
  64. BCC7154 SCH 28080 SCH28080 inhibits gastric H+/K+-ATPase by K+-competitive binding, with an IC50 value of 20 nM in rabbit microsomal membranes. Antisecretory and cytoprotective activities. SCH 28080
  65. BCC6552 DL-AP5 DL-AP5
  66. BCC7717 5-BDBD 5-BDBD
  67. BCC4649 Chlorthalidone Chlorthalidone is a thiazide-like diuretic used to treat hypertension. Chlorthalidone
  68. BCC4014 (+)-MK 801 Maleate Dizocilpine maleate (MK-801 maleate) is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes. (+)-MK 801 Maleate
  69. BCC1327 Acamprosate calcium Acamprosate calcium(Campral EC) is a GABA receptor agonist and modulator of glutamatergic systems; reduces alcohol consumption in animal models of alcohol addiction. Acamprosate calcium
  70. BCC7578 KM 11060 KM11060 is a novel corrector of the F508del-CFTR trafficking defect. KM 11060
  71. BCC3881 PTC124 (Ataluren) Ataluren (PTC124) is an orally available CFTR-G542X nonsense allele inhibitor. PTC124 (Ataluren)
  72. BCC6070 MRK 016 MRK 016
  73. BCC7416 PSB 069 PSB 069
  74. BCC6694 FG 7142 FG 7142 (ZK 39106; LSU-65), a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM). FG 7142 (ZK 39106; LSU-65) also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM). FG 7142 (ZK 39106; LSU-65) can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex. FG 7142
  75. BCC6551 DL-AP7 DL-AP7
  76. BCC6554 L-AP5 L-AP5
  77. BCC6553 D-AP5 D-AP5 is a NMDA receptor antagonist. D-AP5
  78. BCC6625 A-7 hydrochloride A-7 hydrochloride
  79. BCC2036 Vernakalant Vernakalant(RSD-1235) is an investigational mixed ion channel blocker that can terminate acute atrial fibrillation (AF) in humans at 2 to 5 mg/kg and may be more atrial-selective than available agents; in treatment of antiarrhythmic. Vernakalant
  80. BCC5859 Norketamine hydrochloride Norketamine hydrochloride
  81. BCC1301 20-HETE 20-HETE (20-hydroxy Arachidonic Acid) is a CYP450 metabolite and a potent vasoconstrictor. 20-HETE is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles. 20-HETE constricts smooth muscles, stimulates smooth muscle proliferation and migration. 20-HETE increases NADPH oxidase, ROS, and NF-κB activity. 20-HETE also inhibits endothelial NO synthase and inhibits apoptosis of pulmonary artery smooth muscle cells. 20-HETE
  82. BCC6671 Dihydroergotoxine mesylate Dihydroergotoxine mesylate is a complex of closely related alkaloid salts; Binds with high affinity to the GABAA receptor Cl- channel, producing an allosteric interaction with the benzodiazepine site. Dihydroergotoxine mesylate
  83. BCC6559 D-AP7 D-AP7
  84. BCC7668 JNJ 17203212 JNJ-17203212 is a novel and selective TRPV1 antagonist, with IC50 of 65 nM and 102 nM for human TRPV1 and rat TRPV1. JNJ 17203212
  85. BCC6325 SN 2 SN 2 is a novel and potent activator of TRPML3 ion channel with EC50 of 1.8±0.13 μM. SN 2
  86. BCC6140 A 784168 Potent and selective TRPV1 antagonist A 784168
  87. BCC7105 DCPIB DCPIB is a selective, reversible and potent inhibitor of volume-regulated anion channels (VRAC), voltage-dependently activates potassium channels TREK1 and TRAAK, inhibits TRESK, TASK1 and TASK3 (IC50s, 0.14, 0.95, 50.72 μM, respectively). DCPIB is also a selective blocker of swelling-induced chloride current (ICl,swell), with an IC50 of 4.1 μM in CPAE cells. DCPIB
  88. BCC6583 (S)-AMPA (S)-AMPA
  89. BCC6582 (R)-AMPA (R)-AMPA
  90. BCC6222 YM 244769 YM 244769
  91. BCC5051 Lamotrigine Lamotrigine(BW430C) is a novel anticonvulsant drug for inhibition of 5-HT and sodium channel Target: Sodium Channel Lamotrigine stabilises presynaptic neuronal membranes by blockade of voltage-dependent sodium channels, thus preventing the release of excitatory neurotransmitters, particularly glutamate and aspartate [1]. Lamotrigine
  92. BCC7711 Bretazenil Bretazenil
  93. BCC6635 β-CCB β-CCB
  94. BCC5896 MNI-caged-D-aspartate MNI-caged-D-aspartate
  95. BCC1419 Bitopertin Bitopertin is a potent, noncompetitive glycine reuptake inhibitor, inhibits glycine uptake at human GlyT1 with a concentration exhibiting IC50 of 25 nM. Bitopertin
  96. BCC1420 Bitopertin (R enantiomer) Bitopertin R enantiomer (RG1678 R enantiomer; RO4917838 R enantiomer) is the R-enantiomer of Bitopertin. Bitopertin is a potent, noncompetitive glycine reuptake inhibitor, inhibits glycine uptake at human GlyT1 with a concentration exhibiting IC50 of 25 nM. Bitopertin (R enantiomer)
  97. BCC5970 Lorazepam Lorazepam
  98. BCC4277 NBI-98782 NBI-98782(alpha-dihydrotetrabenazine) is a vesicular monoamine transporter (VMAT2) inhibtior with an Ki value of 0.97 nM. NBI-98782
  99. BCC6803 THIP hydrochloride Gaboxadol hydrochloride (Lu 02-030 hydrochloride; THIP hydrochloride) is a potent agonist of the GABAA receptor and an antagonist of GABAC receptors (IC50=25 μM). Gaboxadol hydrochloride displays a partial agonist efficacy on subunit α1β2γ2 with an ED50 value of 143 µM, a full agonist efficacy at α5 subunit (ED50=28-129 µM) and a superagonist efficacy at α4β3δ (ED50=6 µM). Gaboxadol hydrochloride is a non-opioid analgesic and has hypnotic activities. THIP hydrochloride
  100. BCC6044 RuBi-4AP RuBi-4AP
  101. BCC6122 TCN 201 TCN 201

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