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(97 products)
- Adiponectin receptor(5 products)
- CFTR(66 products)
- CGRP Receptor(51 products)
- Calcium Channel(573 products)
- Chloride channel(54 products)
- GABA Receptor(372 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(258 products)
- TRP/TRPV Channel(96 products)
Show 13 more subcategories
Found 2726 products of "Membrane Transporter/Ion Channel"
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GABAA receptor agent 7
CAS:Compound 5c, a GABAA receptor modulator with anticonvulsant properties and low neurotoxicity, is promising for epilepsy research.Formula:C18H13ClN4OColor and Shape:SolidMolecular weight:336.77ZK93423
CAS:ZK93423: potent benzodiazepine agonist, IC50=1nM, non-selective, Ki=4.1-6nM for α1-α5 GABAA subunits.Formula:C23H22N2O4Color and Shape:SolidMolecular weight:390.43AMG-1
CAS:AMG-1 inhibits CRAC channels, blocks effector T cells, not regulatory ones, and reduces EAE progression.Formula:C18H9ClF5N3OColor and Shape:SolidMolecular weight:413.73Efflux inhibitor-1
CAS:Efflux inhibitor-1 is a pyrazolopyrimidine efflux inhibitor.Formula:C28H25N5O3Color and Shape:SolidMolecular weight:479.53(Rac)-NMDAR antagonist 1
CAS:(Rac)-NMDAR antagonist 1 is a racemate of NMDAR antagonist 1. NMDAR antagonist 1 is a potent, orally active, NR2B-selective NMDAR antagonist.Formula:C20H20BrN3O2Color and Shape:SolidMolecular weight:414.3P-gp inhibitor 3
P-gp inhibitor 3 boosts Paclitaxel's effect by strongly reversing MDR via P-gp efflux blockade.Formula:C48H67N3O6Color and Shape:SolidMolecular weight:782.06Clobutinol
CAS:Clobutinol has anti-tussive effects. Clobutinol affects heart rate and blood pressure, it can be used for cough related research [1] [2] [3].Formula:C14H22ClNOColor and Shape:SolidMolecular weight:255.78(R)-Posenacaftor sodium
CAS:(R)-Posenacaftor sodium is a modulator for correcting cystic fibrosis protein folding.Formula:C27H27NNaO5Color and Shape:SolidMolecular weight:468.505P-CAB agent 2 hydrochloride
CAS:P-CAB agent 2 hydrochloride is a strong oral gastric acid secretion inhibitor with IC50 <100 nM on H+/K+ ATPase and 18.69 µM on hERG channel, non-toxic.Formula:C22H26ClFN2O4SColor and Shape:SolidMolecular weight:468.97SK3 Channel-IN-1
CAS:SK3 Channel-IN-1: Potent, selective SK3 modulator; inhibits MDA-MB-435 migration, low cytotoxicity.Formula:C25H49NOColor and Shape:SolidMolecular weight:379.66Xininurad
CAS:Xininurad (XNW3009) is a urate transporter (URAT) inhibitor.Formula:C15H10Br2FN3O2Color and Shape:SolidMolecular weight:443.07MRS-1477
CAS:MRS-1477 is used as a TRPV1 positive allosteric modulator (PAM).Formula:C21H27NO4SPurity:98%Color and Shape:SolidMolecular weight:389.51Cgp 31358
CAS:CGP 31358 is a new chemical that targets the NMDA receptor, potentially aiding in molecular pharmacology research.Formula:C19H19ClN4O2Color and Shape:SolidMolecular weight:370.83(1R,2R)-ML-SI3
CAS:(1R,2R)-ML-SI3 ((-)-trans-ML-SI3) is a selective TRPML1, TRPML2, and TRPML3 inhibitor for the study of neurodegenerative and cardiovascular diseases.Formula:C23H31N3O3SColor and Shape:SolidMolecular weight:429.58GLPG-3221
CAS:GLPG-3221, a potent oral CFTR corrector for cystic fibrosis treatment, has an EC50 of 105 nM.Formula:C30H37F3N2O6Purity:98%Color and Shape:SolidMolecular weight:578.62IDO1-IN-19
CAS:IDO1-IN-19 (Compound 17) is a potent inhibitor of IDO1 and has potential for cancer disease research.Formula:C25H22F4N2O3Color and Shape:SolidMolecular weight:474.45P2X7 receptor antagonist-3
CAS:P2X7 receptor antagonist-3 is a powerful inhibitor of the P2X7 receptor, exhibiting IC50 values of 4.2 nM in humans and 6.8 nM in rats, indicating its highFormula:C17H12ClF3N6OColor and Shape:SolidMolecular weight:408.77FFN200 dihydrochloride
CAS:FFN200 is a vesicular monoamine transporter 2 (VMAT2) substrate that selectively traces monoamine exocytosis in both neuronal cell culture and brain tissue.Formula:C11H14Cl2N2O2Color and Shape:SolidMolecular weight:277.15Ivabradine
CAS:Ivabradine: oral HCN blocker, lowers heart rate without affecting blood pressure, has anticonvulsant and anti-anginal properties.Formula:C27H36N2O5Color and Shape:SolidMolecular weight:468.59SN40
CAS:SN40: AAT inhibitor for cancer research; inhibits hASCT1 (7.29 μM), rASCT2 (2.42 μM), hASCT2 (2.94 μM), EAAT1/EAAC1/EAAT5 (5.55 μM), EAAT2 (24.43 μM).Formula:C18H20N2O2Color and Shape:SolidMolecular weight:296.36
