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(52 products)
- Calcium Channel(562 products)
- Chloride channel(54 products)
- GABA Receptor(370 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(295 products)
- Proton pump(42 products)
- SGLT(31 products)
- Sodium Channel(241 products)
- TRP/TRPV Channel(96 products)
Show 13 more subcategories
Found 2675 products of "Membrane Transporter/Ion Channel"
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(R)-IDHP
CAS:(R)-IDHP, a salvia derivative, relaxes blood vessels by blocking calcium channels, aiding cardiovascular research.Formula:C12H16O5Color and Shape:SolidMolecular weight:240.2517R(18S)-EpETE
CAS:17R(18S)-EpETE: Oxylipin, eicosapentaenoic acid metabolite, activates BKCa channels, has negative chronotropic effects.Formula:C20H30O3Color and Shape:SolidMolecular weight:318.457TRPA1-IN-2
CAS:TRPA1-IN-2 is a potent and orally active TRPA1 inhibitor with an IC50 value of 0.04 µM.TRPA1-IN-2 has anti-inflammatory activity.Formula:C24H25F3N4OPurity:98.93%Color and Shape:SoildMolecular weight:442.48Ref: TM-T77511
1mg56.00€5mg129.00€10mg188.00€25mg319.00€50mg447.00€100mg600.00€200mg807.00€1mL*10mM (DMSO)142.00€Lifarizine FA
Lifarizine FA is a sodium channel blocker used in the treatment of neurological disorders and cardiovascular diseases, study of stroke.Formula:C30H34N4O2Purity:99.55%Color and Shape:SolidMolecular weight:482.62APETx2 TFA
APETx2 TFA from sea anemone is a selective ASIC3 inhibitor with a 63 nM IC50, reversing acid and inflammatory pain.Formula:C198H281F3N54O62S6Color and Shape:SolidMolecular weight:4675.02Jingzhaotoxin III
CAS:NaV1.5 channels blockerFormula:C174H241N47O46S6Purity:98%Color and Shape:SolidMolecular weight:3919.47N-Oleoyl Glutamine
CAS:N-Oleoyl Glutamine (Oleoyl-L-glutamine) antagonizes TRPV1 of the transient receptor potential (TRP) calcium channel.
Formula:C23H42N2O4Purity:99.61%Color and Shape:SolidMolecular weight:410.59Tiludronate disodium hemihydrate
CAS:Tiludronate: an oral bisphosphonate for bone disorder research; inhibits osteoclasts and reduces inflammation.Formula:C14H16Cl2Na4O13P4S2Color and Shape:SolidMolecular weight:743.16(2R,3S,11bS)-Dihydrotetrabenazine
CAS:(2R,3S,11bS)-Tetrabenazine impurity, VMAT inhibitor for movement disorders.
Formula:C19H29NO3Purity:99.29%Color and Shape:SolidMolecular weight:319.44BeKm-1
CAS:Potent, selective hERG (KV11.1) blocker; doesn't affect 14 other K+ channels; extends QTc in rabbit heart dose-dependently.Formula:C174H261N51O52S6Purity:98%Color and Shape:SolidMolecular weight:4091.65Chlorotoxin
CAS:Chlorotoxin: 36-amino acid peptide from deathstalker scorpion venom; blocks small chloride channels.Formula:C158H249N53O47S11Purity:98%Color and Shape:SolidMolecular weight:3995.71PtdIns-(1,2-dioctanoyl) (sodium salt)
CAS:PtdIns phosphates, a minor membrane lipid fraction, are vital for cell signaling. Synthetic PtdIns-(1,2-dioctanoyl) has C8:0 fatty acids and high solubility.Formula:C25H47NaO13PColor and Shape:SolidMolecular weight:609.602BDBM50597431
CAS:BDBM50597431 is an NMDA receptor modulator that may have can be used to study Alzheimer's disease and Parkinson's syndrome.Formula:C27H43F3O2Purity:98.64% - 99.28%Color and Shape:SoildMolecular weight:456.62NF110
CAS:P2X3 antagonistFormula:C41H32N6NaO17S4Purity:98%Color and Shape:SolidMolecular weight:1031.97AR-C141990 hydrochloride
CAS:AR-C141990 HCl inhibits MCT-1 (pKi 7.6) and MCT-2 (pKi 6.6), and has immunosuppressive effects.
Formula:C26H29ClN4O4SColor and Shape:SolidMolecular weight:529.05(S)-JNJ-54166060
CAS:(S)-JNJ-54166060, an enantiomer of JNJ-54166060, functions as a potent antagonist of P2X7 [1].Formula:C20H15ClF4N4OColor and Shape:SolidMolecular weight:438.81Venturicidin A
CAS:Venturicidin A is a macrolide antibiotic.Formula:C41H67NO11Purity:98%Color and Shape:SolidMolecular weight:749.97Brevetoxin-3
CAS:Brevetoxin-3 activates Na+ channels, binding strongly to site 5, preventing their inactivation.Formula:C50H72O14Purity:98%Color and Shape:SolidMolecular weight:897.112AmmTX3
KV4 channel blocker that inhibits A-type K+ current in mouse neurons; requires DPP6 and DPP10 for effect.Formula:C158H262N50O48S6Purity:98%Color and Shape:SolidMolecular weight:3822.47EVT-401
EVT-401 (P2X7 receptor antagonist-1), a purinergic P2X7 receptor antagonist, demonstrates efficacy in combating neuroinflammation [1].Formula:C22H20F4N2O3Color and Shape:SolidMolecular weight:436.4
