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(93 products)
- Adiponectin receptor(5 products)
- CFTR(64 products)
- CGRP Receptor(52 products)
- Calcium Channel(496 products)
- Chloride channel(49 products)
- GABA Receptor(337 products)
- Monoamine Transporter(23 products)
- Monocarboxylate transporter(17 products)
- NKCC(2 products)
- NPC1L1(3 products)
- Na-K-Cl cotransporter(8 products)
- OAT(27 products)
- OCT(7 products)
- P-gp(53 products)
- Potassium Channel(277 products)
- Proton pump(39 products)
- SGLT(30 products)
- Sodium Channel(202 products)
- TRP/TRPV Channel(93 products)
Show 13 more subcategories
Found 2293 products of "Membrane Transporter/Ion Channel"
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HENA
CAS:<p>HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.</p>Formula:C30H48NaO3Purity:98%Color and Shape:SolidMolecular weight:479.701Lanceotoxin A
CAS:<p>Lanceotoxin A is a potent Ip blocker.</p>Formula:C32H44O12Purity:98%Color and Shape:SolidMolecular weight:620.68Dopropidil hydrochloride
CAS:<p>Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris.</p>Formula:C20H36ClNO2Color and Shape:SolidMolecular weight:357.96SCH00013
CAS:<p>SCH00013 is a cardiotonic that enhances myofibrillar Ca++ sensitivity, with notable effects at pH 7.2-7.4.</p>Formula:C18H20N4O2Purity:98%Color and Shape:SolidMolecular weight:324.38GZ4
CAS:<p>GZ4 is a Ca2+ currents inhibitor, acting on cell surface channels.</p>Formula:C11H17NO2Purity:98%Color and Shape:SolidMolecular weight:195.26AFD-21
CAS:<p>AFD-21 is a class I antiarrhythmic that inhibits sodium channels with moderate kinetics.</p>Formula:C28H39NO5Purity:98%Color and Shape:SolidMolecular weight:469.61Hexadecylphosphoserine
CAS:<p>Hexadecylphosphoserine is a representative growth inhibitor.</p>Formula:C19H40NO6PPurity:98%Color and Shape:SolidMolecular weight:409.5Metaphit
CAS:<p>Acylator of PCP and σ-receptors</p>Formula:C18H24N2SPurity:98%Color and Shape:SolidMolecular weight:300.46(S)-Baclofen
CAS:<p>(S)-Baclofen may treat hyperacusis and tinnitus by reducing auditory pathway excitation.</p>Formula:C10H12ClNO2Purity:98%Color and Shape:SolidMolecular weight:213.66AMG7905
CAS:AMG7905 is a modulator of transient receptor potential vanilloid type 1.Formula:C25H24F3N5SPurity:98%Color and Shape:SolidMolecular weight:483.55Ro18-5362
CAS:<p>Ro18-5362 is the less active prodrug of Ro 18-5364.</p>Formula:C22H25N3O2SPurity:98%Color and Shape:SolidMolecular weight:395.52Ceefourin-2
CAS:<p>Ceefourin-2 is a highly selective multidrug resistance protein 4 inhibitor.</p>Formula:C15H9ClF3N3O2Purity:98%Color and Shape:SolidMolecular weight:355.7BDF 9148
CAS:BDF 9148, a Na(+)-channel modulator, increases the contractile force of guinea-pig atria and papillary muscles.Formula:C28H27N3O3Purity:98%Color and Shape:SolidMolecular weight:453.53EO-122
CAS:<p>EO-122, a calcium channel antagonist and sodium channel antagonist, is used potentially for the treatment of arrhythmia.</p>Formula:C16H23ClN2OColor and Shape:SolidMolecular weight:294.82DAA-1097
CAS:<p>DAA-1097 is a novel ligand of peripheral benzodiazepine receptor.</p>Formula:C24H24ClNO3Purity:98%Color and Shape:SolidMolecular weight:409.91Levamlodipine gentisate
CAS:<p>Levamlodipine gentisate, an active amlodipine enantiomer, is a dihydropyridine calcium channel blocker for treating hypertension and angina.</p>Formula:C27H31ClN2O9Purity:98%Color and Shape:SolidMolecular weight:563JTT-552
CAS:<p>JTT-552, a uric acid transporter 1 (URAT1) inhibitor, is used potentially for the treatment of hyperuricemia.</p>Formula:C15H12ClNO3Purity:98%Color and Shape:SolidMolecular weight:289.71(S)-3-Carboxy-4-hydroxyphenylglycine
CAS:<p>group I metabotropic glutamate receptor antagonist and group II mGlu agonist</p>Formula:C9H9NO5Purity:98%Color and Shape:SolidMolecular weight:211.17TAS-4
CAS:<p>TAS-4 is a modulator of metabotropic glutamate receptor 4-positive allosteric.</p>Formula:C12H8Cl2N2OPurity:98%Color and Shape:SolidMolecular weight:267.11Hydroflumethiazide
CAS:<p>Hydroflumethiazide is a thiazide diuretic. It has also shown the activity of anti-hypertensive.</p>Formula:C8H8F3N3O4S2Color and Shape:Crystals SolidMolecular weight:331.29Lombazole
CAS:<p>Lombazole is an antimicrobial agent in the class of imidazole.</p>Formula:C22H17ClN2Color and Shape:SolidMolecular weight:344.84Aladorian
CAS:<p>Aladorian (ARM036), a benzothiazepine, has anti-arrhythmic properties for heart failure and CPVT research.</p>Formula:C12H13NO4SPurity:98%Color and Shape:SolidMolecular weight:267.3Arginylproline
CAS:<p>Arginylproline is a dipeptide composed of arginine and proline. It is an incomplete breakdown product of protein digestion or protein catabolism.</p>Formula:C11H21N5O3Color and Shape:SolidMolecular weight:271.32Ro 8-4304
CAS:Ro 8-4304 Hydrochloride is an antagonist of NMDA receptor with IC50 of 0.4 μMFormula:C21H23FN2O3Purity:98%Color and Shape:SolidMolecular weight:370.42CS476
CAS:<p>CS476 is a potent drug of hypoglycaemic.</p>Formula:C24H29N3O5SPurity:98%Color and Shape:SolidMolecular weight:471.57Fluzinamide
CAS:<p>Fluzinamide (AHR-8559) has anticonvulsant effects on ignited amygdala seizures.</p>Formula:C12H13F3N2O2Purity:99.38% - >99.99%Color and Shape:SolidMolecular weight:274.24Laurinterol
CAS:<p>Laurinterol is an antimicrobial from the marine alga Laurencia okamurai.</p>Formula:C15H19BrOColor and Shape:SolidMolecular weight:295.21BRL 55834
CAS:<p>BRL 55834, a potassium channel activator, has shown to relax airways and vasculature in vivo.</p>Formula:C18H20F5NO3Purity:98%Color and Shape:SolidMolecular weight:393.35S-312-d
CAS:<p>S-312d is a calcium channel antagonist. S-312-d can offer marked neuronal protective effects against ischemic injury.</p>Formula:C20H22N2O4SPurity:98%Color and Shape:SolidMolecular weight:386.46Niguldipine Free Base
CAS:<p>Niguldipine Free Base is a calcium channel blocker and a₁-adrenergic receptor antagonist and a clinical modulator of multidrug resistance.</p>Formula:C36H39N3O6Purity:98.97%Color and Shape:SolidMolecular weight:609.71CGP 28392
CAS:<p>CGP 28392 is used as a partial calcium channel agonist.</p>Formula:C18H17F2NO5Purity:98%Color and Shape:SolidMolecular weight:365.33RH01617
CAS:<p>RH01617 possesses potent inhibitory activities against Kv1.5.</p>Formula:C22H26N2O5SPurity:98%Color and Shape:SolidMolecular weight:430.52Glypromate
CAS:<p>Glypromate (Gly-Pro-Glu) is a neuroprotective agent, is a weak NMDA receptor agonist</p>Formula:C12H19N3O6Purity:98%Color and Shape:SolidMolecular weight:301.3SR57227A
CAS:<p>SR 57227A: Selective 5-HT3 receptor inhibitor, affects NMDA responses, has anti-depressant effects and reduces aggression in rats.</p>Formula:C10H14ClN3Purity:98%Color and Shape:SolidMolecular weight:211.69PNU-107484A
CAS:<p>PNU-107484A is a unique GABA(A) receptor ligand.</p>Formula:C18H23ClN6Purity:98%Color and Shape:SolidMolecular weight:358.87Guanosine 5'-diphosphate ditromethamine
CAS:Guanosine 5'-diphosphate ditromethamine (GDP ditromethamine) is a nucleoside diphosphate that activates ATP-sensitive K+ channels. It acts as a potential iron mobilizer, inhibiting the interaction between hepcidin and ferroportin, and modulating the IL-6/STAT-3 pathway. This compound finds application in inflammation research, such as studying anemia of inflammation (AI).Formula:C18H37N7O17P2Molecular weight:685.47GSK1702934A
CAS:GSK1702934A is a TRPC3 agonist with pro-arrhythmic and positive inotropic effects and is used in the study of diabetes mellitus.Formula:C22H25N3O2SPurity:98.15%Color and Shape:SolidMolecular weight:395.52N-Oleoyl Valine
CAS:N-Oleoyl valine, an N-acyl amine, antagonizes TRPV3 for thermoregulation; rises post-cold exposure; elevates in mouse lung injury.Formula:C23H43NO3Molecular weight:381.59GS 39783
CAS:<p>GS 39783 is a positive allosteric modulator (PAM) of GABABR, which reduces the motivational properties of alcohol and the conditioned reinforcement and</p>Formula:C15H23N5O2SPurity:99.92%Color and Shape:SolidMolecular weight:337.44SM-6586
CAS:SM-6586 is a potent calcium channel antagonist with inhibitory effects on Na+/H+ and Na+/Ca2+ exchange channels, and can be used in the study of cerebrovascularFormula:C26H27N5O5Purity:99.43%Color and Shape:SolidMolecular weight:489.52(5R)-BW-4030W92
CAS:<p>(5R)-BW-4030W92 is the R-type of BW-4030W92, the active enantiomer.</p>Formula:C11H9Cl2FN4Purity:98.27%Color and Shape:SolidMolecular weight:287.12MDL-29951
CAS:MDL-29951 is a novel glycine antagonist of NMDA receptor activation.Formula:C12H9Cl2NO4Purity:98.79% - 99.49%Color and Shape:SolidMolecular weight:302.11YM-900
CAS:YM-900, an AMPA receptor antagonist and glutamate receptor antagonist, is used potentially for the treatment of stroke.Formula:C11H7N5O4Purity:98%Color and Shape:SolidMolecular weight:273.2AM12
CAS:AM12 inhibits Lanthanide-evoked TRPC5 activity (IC50: 0.28 μM).Formula:C15H9BrO5Purity:98%Color and Shape:SolidMolecular weight:349.13ML402
CAS:<p>ML402 (ZINC3671497) is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.</p>Formula:C14H14ClNO2SPurity:99.71%Color and Shape:SolidMolecular weight:295.78Zatebradine hydrochloride
CAS:<p>Zatebradine hydrochloride (UL-FS-49CL) inhibits HCN channels (IC50: ~1.9 µM) blocking human HCN1-4 currents effectively.</p>Formula:C26H37ClN2O5Purity:97%Color and Shape:SolidMolecular weight:493.04Cyclic ADP-ribose
CAS:<p>cADPR, made from NAD+, boosts calcium in cells via Ryanodine receptors and TRPM2 channels.</p>Formula:C15H21N5O13P2Purity:98%Color and Shape:Lyophilized PowderMolecular weight:541.3Bifenazate
CAS:<p>Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.</p>Formula:C17H20N2O3Purity:99.62%Color and Shape:Solid CrystallineMolecular weight:300.35BMS-919373
CAS:<p>BMS-919373 is a potassium channel Kv1.5 (KCNA5) inhibitor for atrial fibrillation and acute coronary syndrome.</p>Formula:C25H20N6O2SPurity:98.51% - 99.01%Color and Shape:SolidMolecular weight:468.53McN5691
CAS:McN5691 is a voltage sensitive calcium channel blocker.Formula:C30H35NO3Purity:98.93% - 99.38%Color and Shape:SolidMolecular weight:457.6Levosemotiadil
CAS:<p>Levosemotiadil（SA 3212） is a novel calcium antagonist and a very potent inhibitor of low-density lipoprotein oxidation.Levosemotiadil may be used to prevent</p>Formula:C29H32N2O6SPurity:98.53% - 99.47%Color and Shape:SolidMolecular weight:536.64(R)-Baclofen hydrochloride
CAS:<p>Arbaclofen HCl, a GABA-B agonist, treats spasticity from spinal injury by reducing excitatory transmission.</p>Formula:C10H13Cl2NO2Purity:98%Color and Shape:SolidMolecular weight:250.12Vernakalant
CAS:<p>Vernakalant (RSD-1235) is a mixed ion channel blocker.</p>Formula:C20H31NO4Purity:98%Color and Shape:SolidMolecular weight:349.46Amsacrine
CAS:<p>Amsacrine (AMSA) (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.</p>Formula:C21H19N3O3SPurity:99.2%Color and Shape:Yellow Crystalline Powder SolidMolecular weight:393.46SCH 50911
CAS:<p>SCH 50911 is a selective GABA(B) receptor antagonist with IC50: 1.1 μM, boosting 3H overflow at IC50: 3 μM.</p>Formula:C8H15NO3Purity:98%Color and Shape:SolidMolecular weight:173.21Phenamil
CAS:<p>Phenamil is an inhibitor of epithelial sodium channels, activates the osteomorphin protein pathway to promote bone repair and induces significant fat formation.</p>Formula:C12H12ClN7OPurity:99.07%Color and Shape:SolidMolecular weight:305.72B-TPMF
CAS:<p>B-TPMF is a highly efficient and selective KCa2.1 channel inhibitor with an IC50 of 31 nM, interacting with serine residue at position 293 to inhibit KCa2.1.</p>Formula:C19H24N6O2Purity:99.82%Color and Shape:SolidMolecular weight:368.43CM-TPMF
CAS:<p>CM-TPMF is a highly efficient and potent activator of the K(Ca)2.1 channel, Ser293 in the transmembrane segment 5, neurological disorders.</p>Formula:C16H17ClN6O2Purity:99.94%Color and Shape:SolidMolecular weight:360.8TTA-Q6
CAS:<p>TTA-Q6 is a T-type Ca2+ channel antagonist that inhibits the uptake of extracellular calcium ions by tumour cells for the treatment of neurological diseases.</p>Formula:C20H15ClF3N3OPurity:99.97%Color and Shape:SolidMolecular weight:405.818:0 LYSO-PE
CAS:<p>18:0 LYSO-PE is a compound that induces an increase in [Ca2+]i and can be used as a phospholipid (PL) standard for lipid analysis by electrospray mass spectrometry (ESI-MS)/MS.</p>Formula:C23H48NO7PPurity:98%Color and Shape:SolidMolecular weight:481.6ABCG2-IN-1
CAS:<p>ABCG2-IN-1 (compound K2), an analog of Ko143, constitutes an orally active inhibitor targeting ABCG2 with an inhibitory concentration (IC50) of 0.13 μM.</p>Formula:C26H36N4O4Purity:98%Color and Shape:SolidMolecular weight:468.59E2730
CAS:<p>E2730 is a non-competitive GABA transporter 1 (GAT1) inhibitor with anti-epileptic activity, useful in studying neurological disorders.</p>Formula:C9H8F4N2O2SPurity:98.22% - 98.54%Color and Shape:SolidMolecular weight:284.23TWIK-1/TREK-1-IN-2
CAS:<p>TWIK-1/TREK-1-IN-2 (Compound 2g) serves as an inhibitor of both TWIK-1 and TREK-1, targeting the TREK-1 homodimer and TWIK-1/TREK-1 heterodimer with IC50 values</p>Formula:C20H29F3N2O2Purity:98%Color and Shape:SolidMolecular weight:386.45ABCG2-IN-2
CAS:<p>ABCG2-IN-2 is a potent inhibitor of ABCG2, exhibiting favorable oral pharmacokinetic profiles in mice, and is applicable for investigating tumor multidrug</p>Formula:C25H34N4O4Purity:98%Color and Shape:SolidMolecular weight:454.56U-89843A
CAS:<p>U-89843A is an allosteric modulator of the GABA_A receptor, known to enhance GABA-induced Cl^- currents [1].</p>Formula:C16H24ClN5Purity:98%Color and Shape:SolidMolecular weight:321.85TWIK-1/TREK-1-IN-1
CAS:<p>Compound 2a, identified as TWIK-1/TREK-1-IN-1, acts as an inhibitor of the TREK-1, a two-pore domain potassium channel (K2p) that forms TREK-1 homodimers and</p>Formula:C21H24F3NO3Purity:98%Color and Shape:SolidMolecular weight:395.42D-3263 hydrochloride
CAS:<p>D-3263 hydrochloride (D3263 HCl salt) is enteric-coated, orally bioavailable transient receptor potential melatonin member 8 (TRPM8) agonist.</p>Formula:C21H32ClN3O3Purity:99.93%Color and Shape:SolidMolecular weight:409.95Vernakalant Hydrochloride
CAS:<p>Vernakalant Hydrochloride (RSD1235 hydrochloride) is a mixed voltage- and frequency-dependent Na+ and atria-preferred K+ channel blocker.</p>Formula:C20H32ClNO4Purity:99.89%Color and Shape:SolidMolecular weight:385.93YHO-13351 free base
CAS:<p>YHO-13351 free base is the water-soluble prodrug of YHO-13177 which is an inhibitor of BCRP .</p>Formula:C26H33N3O4SPurity:99.89%Color and Shape:SolidMolecular weight:483.62Pinacidil
CAS:<p>Pinacidil (P 1134) is a guanidine that opens potassium channels and directly dilates peripheral blood vessels in small arteries, lowering blood pressure and</p>Formula:C13H19N5Purity:99.9%Color and Shape:SolidMolecular weight:245.32TRPV4 agonist-1
CAS:TRPV4 agonist-1 is an agonist of TRPV4 (EC50: 60 nM in the hTRPV4 Ca2+ assay).Formula:C25H23ClF2N4O2Purity:98%Color and Shape:SolidMolecular weight:484.93PF 05089771 tosylate
CAS:<p>PF-05089771 inhibits Nav1.7 channels (IC50: 11-33 nM), selective over Nav1.1-1.6/1.8, Ca+, K+ channels, TRPV1; 1000x affinity for half-inactivated state.</p>Formula:C18H12Cl2FN5O3S2·C7H8O3SPurity:98.55%Color and Shape:SolidMolecular weight:672.56Lesogaberan
CAS:<p>Lesogaberan: selective GABAB agonist, EC50 8.6 nM, Ki 5.1 nM in rats, weak GABAA affinity (Ki 1.4 μM).</p>Formula:C3H9FNO2PPurity:98%Color and Shape:SolidMolecular weight:141.08UK 78282 hydrochloride
CAS:UK-78282 hydrochloride, a Kv1.3 blocker.UK-78282 hydrochloride inhibits Kv1.3 voltage-gated potassium channels and suppresses human T cell activation.Formula:C29H36ClNO2Purity:99.89%Color and Shape:SolidMolecular weight:466.05Puliginurad
CAS:<p>Puliginurad (YL-90148) is a urate transporter protein inhibitor that inhibits the reabsorption of uric acid.Puliginurad is used in the treatment of gout.</p>Formula:C19H16N2O2SPurity:99.96% - 99.96%Color and Shape:SolidMolecular weight:336.41GX-674
CAS:<p>GX-674 is a highly potent and selective voltage-gated sodium channel 1.7 (Nav1.7) antagonist with an IC50 value of 0.1 nM measured at -40 mV for the study of</p>Formula:C21H13ClF2N6O3S2Purity:98.60%Color and Shape:SolidMolecular weight:534.95TRAM 39
CAS:<p>TRAM 39 (2-Chloro-α,α-diphenylbenzeneacetonitrile) is a selective blocker of intermediate-conductance Ca2+-activated K+channels.</p>Formula:C20H14ClNPurity:99.97%Color and Shape:SolidMolecular weight:303.78Tracazolate hydrochloride
CAS:<p>Tracazolate hydrochloride (Tracazolate (hydrochloride)) is a modulator of the GABAA receptor with anxiolytic and anticonvulsant activity.</p>Formula:C16H25ClN4O2Purity:99.52%Color and Shape:SolidMolecular weight:340.85TRPM4-IN-2
CAS:NBA, or TRPM4-IN-2, is a potent TRPM4 inhibitor with IC50 of 0.16 μM, used in prostate and colorectal cancer research.Formula:C19H14ClNO4Purity:99.21%Color and Shape:SolidMolecular weight:355.77RO 4938581
CAS:RO 4938581: potent GABAA α5 inverse agonist (Ki 4.6 nM); lower affinity for α1β3γ2a, α2β3γ2a, α3β3γ2a (Ki: 174, 185, 80 nM).Formula:C13H8BrF2N5Purity:98%Color and Shape:SolidMolecular weight:352.14JYL 1421
CAS:<p>JYL 1421 (SC 0030) is an antagonist of TRPV1 receptor (IC50 = 8 nM).</p>Formula:C20H26FN3O2S2Purity:98.83%Color and Shape:SolidMolecular weight:423.57GDC-0276
CAS:<p>GDC-0276 is an orally active, selective, and potent NaV1.7 inhibitor that can be used for the study of pain-related diseases.</p>Formula:C24H31FN2O4SPurity:99.77%Color and Shape:SolidMolecular weight:462.58RY796
CAS:<p>RY796 is a selective voltage-gated potassium (KV2) channel inhibitor that inhibits KV2.1 and KV2.2, used in research on neurological disorders.</p>Formula:C21H27N3O2Purity:98.59%Color and Shape:SolidMolecular weight:353.46RN9893
CAS:RN9893 is a selective and potent TRPV4 receptor antagonist with IC50 values of 320, 420 and 660 nM for TRPV4 receptors in mouse, human and rat, respectively.Formula:C21H23F3N4O5SPurity:99.99%Color and Shape:SolidMolecular weight:500.49ATX-II TFA
<p>ATX-II TFA, a specific Na+ channel modulator toxin, is derived from the venom of the sea anemone (Anemonia sulcata).</p>Purity:98%Color and Shape:Odour SolidAZD 3043
CAS:<p>AZD 3043 (THRX 918661) is a modulator of the gamma-aminobutyric acid type A receptor, a novel sedative-hypnotic, and a potential short-acting anesthetic.</p>Formula:C19H29NO5Purity:98.19% - 99.55%Color and Shape:SolidMolecular weight:351.44E 0747
CAS:<p>E 0747 is an antiarrhythmic agent of class 1C type. E-0747 suppresses arrhythmia by inhibiting the Na channels of cardiac cells.</p>Formula:C21H28ClN3O4Purity:95.17%Color and Shape:SolidMolecular weight:421.92TRPV3 antagonist 74a
CAS:<p>TRPV3 antagonist 74a (TRPV3 74a) is a specific TRPV3 antagonist for the study of neurological disorders.</p>Formula:C17H17F3N2O2Purity:≥98.0%Color and Shape:SolidMolecular weight:338.32AVE1231
CAS:AVE1231 is a TASK-1 channel blocker that inhibits TASK-1 and can be used in the study of atrial fibrillation.Formula:C20H27N3O4SPurity:98.03%Color and Shape:SolidMolecular weight:405.51Phaclofen
CAS:<p>GABAB antagonist</p>Formula:C9H13ClNO3PPurity:99.32%Color and Shape:White SolidMolecular weight:249.63GAL-021 sulfate
CAS:GAL-021 sulfate is a BKCa channel blocker that inhibits the analgesic effects of opioids and is used in the study of respiratory control diseases.Formula:C11H24N6O5SPurity:99.92%Color and Shape:SolidMolecular weight:352.41Istaroxime hydrochloride
CAS:<p>Istaroxime hydrochloride (PST2744 hydrochloride) is a Na+/K+-ATPase inhibitor and SERCA 2 activator, and is a novel positive inotropic compound.</p>Formula:C21H33ClN2O3Color and Shape:SolidMolecular weight:396.95GX-585
CAS:<p>GX-585 is a novel potent inhibitor of NaV1.7 and highly selective against NaV1.5, having limited selectivity against NaV1.1 and NaV1.2.</p>Formula:C24H25Cl2FN4O3SPurity:99.02% - 99.03%Color and Shape:SolidMolecular weight:539.45SRI-37240
CAS:SRI-37240 suppresses CFTR nonsense mutations, aids in fixing premature termination codons, works with G418.Formula:C24H23N3O2Purity:98.73%Color and Shape:SolidMolecular weight:385.46AGN-201904
CAS:AGN-201904 is a proton pump inhibitor, an omeprazole prodrug, which delays aging and may be used for the prevention and treatment of peptic ulcers.Formula:C25H25N3O8S2Purity:97.32%Color and Shape:SolidMolecular weight:559.61Ani9
CAS:<p>Ani9 selectively blocks ANO1/TMEM16A with a 77 nM IC50, useful for ANO1 research and treating cancer, hypertension, pain, diarrhea, asthma.</p>Formula:C17H17ClN2O3Purity:99.73%Color and Shape:SolidMolecular weight:332.78Suriclone
CAS:<p>Suriclone (RP 31264), a cyclic pyrrolidone for anxiety, modulates GABA-A receptors without major sedation.</p>Formula:C20H20ClN5O3S2Purity:99.21% - 99.73%Color and Shape:SolidMolecular weight:477.99S 18986
CAS:<p>S 18986 is a selective, orally active, brain penetrant positive allosteric modulator of AMPA-type receptors, showcasing cognitive-enhancing properties in</p>Formula:C10H12N2O2SPurity:99.64%Color and Shape:SolidMolecular weight:224.28Quinabactin
CAS:<p>Quinabactin (LC-66C6): ABA agonist, induces guard cell closure, reduces water loss, hinders germination, boosts drought resistance in Arabidopsis/soybean.</p>Formula:C20H24N2O3SPurity:99.63%Color and Shape:SolidMolecular weight:372.48AV-101
CAS:<p>AV-101 (4-Cl-KYN) is a prodrug antagonist at the glycine site of the NMDA receptor with antidepressant activity that reduces dyskinesia.</p>Formula:C10H11ClN2O3Purity:97.78% - 98.27%Color and Shape:SolidMolecular weight:242.66
