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(259 products)
- TRP/TRPV Channel(96 products)
Show 13 more subcategories
Found 2722 products of "Membrane Transporter/Ion Channel"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
TRPC6-IN-1
CAS:TRPC6-IN-1 is an inhibitor of the Transient Receptor Potential Canonical 6 Channel (TRPC6) (EC50: 4.66 μM).Formula:C21H23FN4O3Purity:98%Color and Shape:SolidMolecular weight:398.43F15845
CAS:F 15845: potent sodium current blocker, anti-ischemic, offers short/long-term post-infarction cardioprotection.Formula:C20H25NO2S2Color and Shape:SolidMolecular weight:375.55SNAP
CAS:NO donorFormula:C7H12N2O4SPurity:99.49%Color and Shape:Green Crystalline SolidMolecular weight:220.255,7-Dichlorokynurenic acid sodium salt
CAS:5,7-Dichlorokynurenic acid sodium salt is a NMDA receptor antagonist.Formula:C10H5Cl2NNaO3Purity:98%Color and Shape:SolidMolecular weight:281.05Traxoprodil Mesylate
CAS:Traxoprodil Mesylate is a potent noncompetitive N-methyl-D-aspartate (NMDA) receptors antagonist and has selective for the NR2B subunit.Formula:C21H29NO6SPurity:98%Color and Shape:SolidMolecular weight:423.52Ro 04-5595 free base
CAS:"Ro 04-5595: Selective NMDA NR2B antagonist, EC50 186nmol/L; binds EVT-101 site; hierarchy of inhibition affinity observed."Formula:C19H22ClNO2Color and Shape:SolidMolecular weight:331.84AM12
CAS:AM12 inhibits Lanthanide-evoked TRPC5 activity (IC50: 0.28 μM).Formula:C15H9BrO5Purity:98%Color and Shape:SolidMolecular weight:349.13NS 3763
CAS:NS 3763 is a kainate receptor antagonist.Formula:C22H16N2O6Purity:98%Color and Shape:SolidMolecular weight:404.37RS-93522
CAS:RS-93522: Calcium channel antagonist, inhibits phosphodiesterase (IC50=1.6x10^-5M), like milrinone, and has a negative inotropic effect.Formula:C27H30N2O9Purity:98%Color and Shape:SolidMolecular weight:526.54Remacemide hydrochloride
CAS:Remacemide hydrochloride is a NMDA receptor antagonist.Formula:C17H21ClN2OPurity:98%Color and Shape:SolidMolecular weight:304.81ARN23746
CAS:ARN23746 is a NKCC1 Inhibitor for the Treatment of Core Symptoms in Down Syndrome.Formula:C17H25F3N2O4SColor and Shape:SolidMolecular weight:410.45LY382884
CAS:LY382884 is a selective and potent GluR5 kainate receptor antagonist with anxiolytic activity.LY382884 blocks blockade of mossy fibre LTP induction.Formula:C18H23NO4Purity:98.32% - 98.71%Color and Shape:SolidMolecular weight:317.38Ciclotizolam
CAS:Ciclotizolam, a thienotriazolodiazepine derivative and partial GABAA receptor agonist, has low efficacy but similar affinity as brotizolam.Formula:C20H18BrClN4SColor and Shape:SolidMolecular weight:461.81CGS8216
CAS:CGS8216 shows analgesic activity at high doses, has anxiolytic activity, and can be used to study immune system disorders.Formula:C16H11N3OPurity:98.53%Color and Shape:SolidMolecular weight:261.28Besonprodil
CAS:Besonprodil is a drug that acts as an NMDA antagonist and is selective for the NR2B subunit.Formula:C21H23FN2O3SColor and Shape:SolidMolecular weight:402.48ATPase-IN-2
CAS:ATPase-IN-2: ATPase inhibitor (IC50 = 0.9μM), also blocks C. difficile toxin B (AC50 = 30.91μM). Used in ATP research.Formula:C22H20N2O4Color and Shape:SolidMolecular weight:376.41Ro 19-4603
CAS:Benzodiazepine inverse agonistFormula:C15H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:319.38Budipine Hydrochloride
CAS:Budipine is an antiparkinsonian that enhances dopamine release, inhibits MAO-B, blocks dopamine reuptake, and stimulates AADC.Formula:C21H28ClNPurity:98%Color and Shape:SolidMolecular weight:329.91ATPA
CAS:ATPA activates GluR5 glutamate receptors; EC50s range 0.66-32 μM across GluR5 variants.Formula:C10H16N2O4Purity:98%Color and Shape:SolidMolecular weight:228.24AJG-049 free base
CAS:AJG-049 free base is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).Formula:C27H30N2O2Color and Shape:SolidMolecular weight:414.54
