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(98 products)
- Adiponectin receptor(5 products)
- CFTR(66 products)
- CGRP Receptor(55 products)
- Calcium Channel(575 products)
- Chloride channel(54 products)
- GABA Receptor(373 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(55 products)
- Potassium Channel(304 products)
- Proton pump(42 products)
- SGLT(31 products)
- Sodium Channel(257 products)
- TRP/TRPV Channel(95 products)
Show 13 more subcategories
Found 2737 products of "Membrane Transporter/Ion Channel"
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(R)-Lercanidipine hydrochloride
CAS:(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.Formula:C36H42ClN3O6Purity:98%Color and Shape:SolidMolecular weight:648.2AMG8788
CAS:AMG8788 is a selective, potent and orally active TRPM8 antagonist (IC50: 63.2 nM).Formula:C23H18F4N2OColor and Shape:SolidMolecular weight:414.4V116517
CAS:V-116517, a TRPV1 antagonist, is used potentially for the treatment of severe pain due to osteoarthritis and chronic pain due postherpetic neuralgia (PHN).Formula:C19H18ClF3N4O3Color and Shape:SolidMolecular weight:442.82GSK-5498A
CAS:GSK-5498A: Selective CARC blocker, inhibits release of mediators from mast cells and cytokines from T-cells (IC50, 1 μM).Formula:C18H11F6N3OColor and Shape:SolidMolecular weight:399.29McN5691
CAS:McN5691 is a voltage sensitive calcium channel blocker.Formula:C30H35NO3Purity:98.93% - 99.38%Color and Shape:SolidMolecular weight:457.6Semotiadil recemate fumarate
CAS:Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel antagonist of vasoselective Ca2+ channel.Formula:C33H36N2O10SPurity:98%Color and Shape:SolidMolecular weight:652.71GW791343 trihydrochloride
CAS:GW791343 trihydrochloride (GW791343 3HCl) is aHCl salt form of GW791343, which is a non-competitive allosteric modulator of human P2X7 receptor inhibitor withFormula:C20H24F2N4O·3HClPurity:98%Color and Shape:SolidMolecular weight:483.81AMPA receptor modulator-4
CAS:AMPA Receptor Modulator-4, a 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide (BTD), serves as an orally active positive allosteric modulator of the AMPAFormula:C11H12ClFN2O2SPurity:98%Color and Shape:SolidMolecular weight:290.74GABAA receptor agent 6
CAS:GABAA receptor agent 6 (compound 2027) is a potent γ-GABAAR antagonist with low cellular membrane permeability (Ki = 0.56 μM) [1].Formula:C18H25N3O2Color and Shape:SolidMolecular weight:315.41Almokalant
CAS:Almokalant: Class III antiarrhythmic, K+ channel blocker, inhibits Ikr current.Formula:C18H28N2O3SPurity:98%Color and Shape:SolidMolecular weight:352.49FG8119
CAS:FG8119 is a novel benzodiazepine agonist with potential anticonvulsant and antiepileptic activity for the study of neurological disorders.Formula:C17H15N5O2Purity:>99.99%Color and Shape:SolidMolecular weight:321.33PF-05214030
CAS:PF-05214030 is a novel potent TRPV4 antagonist (hTRPV4 IC50 4nM; rTRPV4 IC50 27nM).Formula:C17H13Cl2FN2O4SColor and Shape:SolidMolecular weight:431.27UoS 12258
CAS:UoS 12258 is a positive allosteric modulator of AMPA receptors, used for studying cognitive impairments.Formula:C17H19FN2O2SPurity:99.84% - 99.89%Color and Shape:SolidMolecular weight:334.41CaV1.3 antagonist-1
CAS:CaV1.3 antagonist-1 is a selective CaV1.3L-type calcium channel antagonist useful for researching neurological disorders and cardiovascular diseases.Formula:C17H19ClN2O3Color and Shape:SolidMolecular weight:334.8(RS)-CPP
CAS:(RS)-CPP is a NMDA antagonist.Formula:C8H17N2O5PPurity:98%Color and Shape:SolidMolecular weight:252.2Quinine hemisulfate
CAS:Quinidine: antiarrhythmic, orally active, inhibits cytochrome P450db, blocks K+ channels (IC50: 19.9μM), may aid in malaria research.Formula:C40H50N4O8SPurity:98%Color and Shape:SolidMolecular weight:746.92Levosemotiadil
CAS:Levosemotiadil（SA 3212） is a novel calcium antagonist and a very potent inhibitor of low-density lipoprotein oxidation.Levosemotiadil may be used to preventFormula:C29H32N2O6SPurity:98.53% - 98.88%Color and Shape:SolidMolecular weight:536.64D-NMAPPD
CAS:Litifilimab (BIIB059) is a humanized antibody targeting BDCA2 and CLEC4C for the study of cutaneous lupus erythematosus.Formula:C23H38N2O5Color and Shape:SolidMolecular weight:422.56UT-B-IN-1
CAS:UT-B-IN-1: reversible UT-B inhibitor, IC50: 10 nM (human), 25 nM (mouse), low toxicity, diuretic research tool.Formula:C20H17N5O2S3Color and Shape:SolidMolecular weight:455.58GSK-5503A
CAS:GSK-5503A is a novel channel blocker of CRAC.Formula:C23H17F2N3O2Purity:98%Color and Shape:SolidMolecular weight:405.4
