
Membrane Transporter/Ion Channel
Membrane transporter and ion channel inhibitors are compounds that block the function of proteins responsible for the transport of ions, nutrients, and other molecules across cell membranes. These inhibitors are crucial for studying the regulation of cellular homeostasis, signal transduction, and neurotransmission. Membrane transporter and ion channel inhibitors are also important in developing treatments for disorders such as epilepsy, cardiovascular diseases, and metabolic syndromes. At CymitQuimica, we provide a diverse selection of high-quality membrane transporter and ion channel inhibitors to support your research in physiology, neuroscience, and pharmacology.
Subcategories of "Membrane Transporter/Ion Channel"
- ABC(3 products)
- ATPase(101 products)
- Adiponectin receptor(5 products)
- CFTR(65 products)
- CGRP Receptor(54 products)
- Calcium Channel(541 products)
- Chloride channel(53 products)
- GABA Receptor(365 products)
- Monoamine Transporter(30 products)
- Monocarboxylate transporter(18 products)
- NKCC(2 products)
- NPC1L1(3 products)
- Na-K-Cl cotransporter(10 products)
- OAT(32 products)
- OCT(7 products)
- P-gp(54 products)
- Potassium Channel(280 products)
- Proton pump(42 products)
- SGLT(31 products)
- Sodium Channel(209 products)
- TRP/TRPV Channel(95 products)
Show 13 more subcategories
Found 2512 products of "Membrane Transporter/Ion Channel"
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(S)-(-)-5-Fluorowillardiine hydrochloride
CAS:(S)-(-)-5-Fluorowillardiine hydrochloride is a potent and specific agonist of AMPAR.Formula:C7H9ClFN3O4Color and Shape:SolidMolecular weight:253.62Delucemine Free Base
CAS:Delucemine Free Base is an NMDA Receptor AntagonistFormula:C16H17F2NColor and Shape:SolidMolecular weight:261.31VU0810464
CAS:VU0810464 is a non-ureaG protein-gated inwardly-rectifying potassium channels (GIRK, Kir3) activator.Formula:C18H21ClFN3OPurity:99.62%Color and Shape:SolidMolecular weight:349.83Ref: TM-T7899
1mg47.00€5mg95.00€10mg150.00€25mg245.00€50mg325.00€100mg434.00€200mg590.00€1mL*10mM (DMSO)104.00€Radiprodil
CAS:Radiprodil (RGH-896) is an oral NMDA NR2B antagonist for potential DPNP neuropathic pain treatment.Formula:C21H20FN3O4Purity:99.74%Color and Shape:SolidMolecular weight:397.4Ref: TM-T5385
1mg48.00€2mg65.00€5mg96.00€10mg153.00€25mg240.00€50mg354.00€100mg532.00€1mL*10mM (DMSO)96.00€Ralfinamide
CAS:Ralfinamide (Priralfinamide) is an orally available Na-channel blocker for the treatment of neuropathic pain and other pain conditions.Formula:C17H19FN2O2Purity:99.41%Color and Shape:SolidMolecular weight:302.34Loreclezole
CAS:Loreclezole is a selective GABAA receptor modulator and acts as a positive allosteric modulator of β2 or β3-subunit-containing receptors.Formula:C10H6Cl3N3Purity:99.78%Color and Shape:SolidMolecular weight:274.53KCNQ2/3 activator-1
CAS:KCNQ2/3 activator-1 is a Kv7.2/Kv7.3 (KCNQ2/3) potassium channel activator.Formula:C23H29FN2OPurity:99.16% - 99.47%Color and Shape:SolidMolecular weight:368.49Ref: TM-T9400
2mg40.00€5mg62.00€10mg94.00€25mg153.00€50mg235.00€100mg373.00€500mg938.00€1mL*10mM (DMSO)67.00€XEN907
CAS:XEN907 is a novel spiro oxindole NaV1.7 blocker. XEN907 also inhibits hNaV1.7 (IC50: 3 nM).Formula:C21H21NO4Purity:99.92%Color and Shape:SolidMolecular weight:351.4Tegoprazan
CAS:Tegoprazan is an orally active, highly selective gastric H+/K+-ATPase inhibitor.Cost-effective and quality-assured.Formula:C20H19F2N3O3Purity:98.22%Color and Shape:SolidMolecular weight:387.38Ref: TM-T17030
1mg52.00€5mg120.00€10mg180.00€25mg298.00€50mg393.00€100mg512.00€200mg727.00€1mL*10mM (DMSO)133.00€Esomeprazole magnesium salt
CAS:<p>Esomeprazole magnesium, an oral proton pump inhibitor, curbs gastric acid by blocking H+, K+-ATPase; used in treating GERD.</p>Formula:C17H21MgN3O3SColor and Shape:SolidMolecular weight:371.74GNE-131
CAS:GNE-131 is a potent and specific inhibitor of human sodium channel NaV1.7 (IC50: 3 nM).Formula:C23H30N4O3SPurity:98.54% - 99.59%Color and Shape:SolidMolecular weight:442.57Ref: TM-TQ0014
1mg111.00€5mg264.00€10mg376.00€25mg630.00€50mg880.00€100mg1,169.00€1mL*10mM (DMSO)283.00€Indecainide hydrochloride
CAS:Indecainide hydrochloride is a cardiac depressant.Formula:C20H25ClN2OColor and Shape:SolidMolecular weight:344.88AZD-9056 free base
CAS:AZD9056 is a potent, selective, orally bioavailable P2X7 receptor antagonist.Formula:C24H35ClN2O2Color and Shape:SolidMolecular weight:419Zosuquidar
CAS:Zosuquidar (RS 33295-198) is a potent P-glycoprotein inhibitor with antitumor activity that inhibits tumor growth.Formula:C32H31F2N3O2Purity:99.99%Color and Shape:SolidMolecular weight:527.6Ref: TM-T6018L
1mg78.00€5mg160.00€10mg233.00€25mg378.00€50mg567.00€100mg825.00€200mg1,130.00€1mL*10mM (DMSO)180.00€Cinacalcet metabolite M4
CAS:<p>Cinacalcet metabolite M4 (Rarechem AL BW 1078) is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.</p>Formula:C10H12F3NPurity:97.13%Color and Shape:SolidMolecular weight:203.2Acecainide hydrochloride
CAS:Acecainide hydrochloride (NAPA) is the major hepatic metabolite of procainamide.Cost-effective and quality-assured.Formula:C15H24ClN3O2Purity:98.023% - 99.81%Color and Shape:SolidMolecular weight:313.83PF 05089771
CAS:PF 05089771 is a Selective inhibitor of Nav1.7 (IC50 = 11 nM) that interacts with the voltage-sensor domain of domain IV.Formula:C18H12Cl2FN5O3S2Purity:99.03% - 99.42%Color and Shape:SolidMolecular weight:500.35Triclabendazole sulfoxide
CAS:<p>TCBZ-SO, a Triclabendazole metabolite, blocks ABCG2/BCRP and has anti-parasitic properties.</p>Formula:C14H9Cl3N2O2SPurity:98.02%Color and Shape:SolidMolecular weight:375.665,7-Dichlorokynurenic acid
CAS:5,7-Dichlorokynurenic acid (5,7-dichlorokynurenic acid sodium) is an NMDA receptor antagonist.Formula:C10H5Cl2NO3Purity:99.71%Color and Shape:SolidMolecular weight:258.06ML277
CAS:ML277 (CID-53347902) was identified as a potent activator of KCNQ1 channels (EC(50)=260 nM).Formula:C23H25N3O4S2Purity:99.35%Color and Shape:SolidMolecular weight:471.59
