Transportador de Membranas/Canal Iónico
Os inibidores de transportadores de membrana e canais iônicos são compostos que bloqueiam a função de proteínas responsáveis pelo transporte de íons, nutrientes e outras moléculas através das membranas celulares. Esses inibidores são cruciais para o estudo da regulação da homeostase celular, transdução de sinais e neurotransmissão. Os inibidores de transportadores de membrana e canais iônicos também são importantes no desenvolvimento de tratamentos para distúrbios como epilepsia, doenças cardiovasculares e síndromes metabólicas. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade de transportadores de membrana e canais iônicos para apoiar sua pesquisa em fisiologia, neurociência e farmacologia.
Subcategorias de "Transportador de Membranas/Canal Iónico"
- ABC(3 produtos)
- ATPase(93 produtos)
- Receptor de adiponectina(5 produtos)
- CFTR(64 produtos)
- Receptor CGRP(51 produtos)
- Canais de Cálcio(494 produtos)
- Canal de cloreto(49 produtos)
- Receptor GABA(336 produtos)
- Transportador de monoamina(23 produtos)
- Transportador de monocarboxilato(17 produtos)
- NKCC(2 produtos)
- NPC1L1(3 produtos)
- Cotransportador Na-K-Cl(8 produtos)
- OAT(27 produtos)
- OCT(7 produtos)
- P-gp(53 produtos)
- Canal de Potássio(276 produtos)
- Bomba de prótons(39 produtos)
- SGLT(30 produtos)
- Canal de Sódio(202 produtos)
- Canal TRP/TRPV(93 produtos)
Exibir 13 mais subcategorias
Foram encontrados 2280 produtos de "Transportador de Membranas/Canal Iónico"
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Glisoxepide
CAS:<p>Glisoxepide: sulphonamide, oral K(ATP) blocker, antihyperglycemic, affects heart.</p>Fórmula:C20H27N5O5SPureza:98%Cor e Forma:SolidPeso molecular:449.52Tedisamil
CAS:<p>Tedisamil blocks cardiac K+ currents, slows heart rate, is a class III antiarrhythmic, and treats angina.</p>Fórmula:C19H32N2Pureza:98%Cor e Forma:SolidPeso molecular:288.47NP-252
CAS:<p>NP-252 is a calcium channel antagonist potentially for the treatment of angina pectoris and congestive heart failure.</p>Fórmula:C26H35N3O5Pureza:98%Cor e Forma:SolidPeso molecular:469.57UBP684
CAS:<p>UBP684 enhances NMDAR responses, boosts l-glutamate/glycine, and mildly affects subunit agonist potency.</p>Fórmula:C17H20O2Pureza:98%Cor e Forma:SolidPeso molecular:256.34Fenazinel Dihydrochloride
CAS:<p>Fenazinel Dihydrochloride, a N-methyl-D-aspartate (NMDA) receptor antagonist, is used potentially for the treatment of ischemic stroke.</p>Fórmula:C21H27Cl2N3O2Cor e Forma:SolidPeso molecular:424.36β-Neuroprotectin
CAS:<p>beta-Neuroprotectin is a (3H)TCP binding inhibitor and provides protection against NMDA mediated neuronal cell death at low concentration.</p>Fórmula:C37H60N8O10Pureza:98%Cor e Forma:SolidPeso molecular:776.92U 90042
CAS:<p>GABAA receptor ligand</p>Fórmula:C17H13ClN6OPureza:98%Cor e Forma:SolidPeso molecular:352.78MRS 2219
CAS:<p>P2X1 receptor potentiator</p>Fórmula:C8H10NO5PPureza:98%Cor e Forma:SolidPeso molecular:231.14COR627
CAS:<p>COR627 is the GABA receptor positive allosteric modulator.</p>Fórmula:C20H27NO3SPureza:98%Cor e Forma:SolidPeso molecular:361.5trans-4-Hydroxycrotonic acid
CAS:<p>ligand of γ-hydroxybutyric acid (GHB) receptor</p>Fórmula:C4H6O3Pureza:98%Cor e Forma:SolidPeso molecular:102.09LY 81067
CAS:<p>LY 81067, a new anticonvulsant, prevents PTZ- and picrotoxin-induced seizures in mice via picrotoxin site interaction.</p>Fórmula:C22H24N4OCor e Forma:SolidPeso molecular:360.45AMG8163
CAS:<p>AMG8163 is an antagonist of vanilloid receptor TRPV1.</p>Fórmula:C25H22F3N5O4SCor e Forma:SolidPeso molecular:545.53AH-1058 HCl
CAS:<p>AH-1058 HCl is a lipophilic antiarrhythmic calcium channel blocker.</p>Fórmula:C30H29ClN2O3Pureza:98%Cor e Forma:SolidPeso molecular:501.02Watanidipine dihydrochloride
CAS:<p>Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.</p>Fórmula:C41H44Cl2N4O6Pureza:98%Cor e Forma:SolidPeso molecular:759.73Kv1.5-IN-IIII
CAS:<p>Kv1.5-IN-IIII is a potent inhibitor of Kv1.5.</p>Fórmula:C25H23ClN4O4SCor e Forma:SolidPeso molecular:510.99Evenamide HCl
CAS:<p>Evenamide, a nav sodium channel blocker, is used potentially for the treatment of schizophrenia.</p>Fórmula:C16H27ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:314.85Gallopamil, (-)-
CAS:<p>Gallopamil, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.</p>Fórmula:C28H40N2O5Pureza:98%Cor e Forma:SolidPeso molecular:484.63DS1
CAS:<p>DS1 is a GABAA receptor agonist which can stimulate gonadotropin subunit gene expression in mouse.</p>Fórmula:C18H10Br2ClN3OSCor e Forma:SolidPeso molecular:511.62Pradigastat sodium
CAS:<p>Pradigastat sodium is a novel inhibitor of DGAT-1.</p>Fórmula:C25H24F3N3NaO2Pureza:98%Cor e Forma:SolidPeso molecular:478.471KR-31378
CAS:<p>KR-31378, a K(ATP) channel activator, is used potentially for the treatment of ocular hypertension and glaucoma.</p>Fórmula:C22H27N5O4Cor e Forma:SolidPeso molecular:425.48MCC1189
CAS:<p>MCC1189 is a first-in-class MFS efflux pump CaMdr1p inhibitor.</p>Fórmula:C22H20N2O2Cor e Forma:SolidPeso molecular:344.41AK-2-38
CAS:<p>AK-2-38 is a nifedipine analogue with potent smooth muscle calcium antagonist action and partial agonist effects on isolated guinea pig left atrium.</p>Fórmula:C26H30N2O4Pureza:98%Cor e Forma:SolidPeso molecular:434.53Azeloprazole
CAS:<p>Azeloprazole, a proton pump inhibitor, is used potentially for the treatment of gastroesophageal reflux disease (GERD).</p>Fórmula:C22H27N3O4SPureza:98%Cor e Forma:SolidPeso molecular:429.53Falipamil
CAS:<p>Falipamil, a verapamil derivative, is a calcium channel blocker with antitachycardic and potential antianginal effects.</p>Fórmula:C24H32N2O5Pureza:98%Cor e Forma:SolidPeso molecular:428.52SGE-201
CAS:<p>SGE-201 is an NMDA receptor allosteric modulator, revealing blocker differences via activity suppression and neuroprotection.</p>Fórmula:C26H44O2Pureza:98%Cor e Forma:SolidPeso molecular:388.63Pentisomide
CAS:<p>Pentisomide: class-I antiarrhythmic, affects depolarization & repolarization, inhibits ischemia-reperfusion arrhythmias, in phase II trials.</p>Fórmula:C19H33N3OPureza:98%Cor e Forma:SolidPeso molecular:319.48NSC339614 potassium
CAS:<p>NSC339614 potassium is a selective GluN1/GluN2C and GluN1/GluN2D receptors potentiator.</p>Fórmula:C10H5KN3O6SPureza:98%Cor e Forma:SolidPeso molecular:334.32JY-XHe-053
CAS:<p>JY-XHe-053 is a selective modulator of GABAA receptors.</p>Fórmula:C22H16FN3O2Pureza:98%Cor e Forma:SolidPeso molecular:373.38HIE-124
CAS:<p>HIE-124 is a central cervous system active anticonvulsant and ultra-short acting hypnotic.</p>Fórmula:C10H12N2O3SPureza:98%Cor e Forma:SolidPeso molecular:240.28Gallopamil HCl, (-)-
CAS:<p>Gallopamil HCl, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.</p>Fórmula:C28H41ClN2O5Pureza:98%Cor e Forma:SolidPeso molecular:521.09Suclofenide
CAS:<p>Suclofenide: a benzenesulfonamide anticonvulsant, effective in mouse seizure models, with side effects like lethargy and diarrhea.</p>Fórmula:C16H13ClN2O4SPureza:98%Cor e Forma:SolidPeso molecular:364.8PD 122860
CAS:<p>PD 122860 is a dihydropyridine enhancing heart contractility, altering ECG, and relaxing aortic rings.</p>Fórmula:C23H20F3N3O4SPureza:98%Cor e Forma:SolidPeso molecular:491.48Oe-9000
CAS:<p>Oe-9000 blocks voltage-gated Na(+) currents in neurons at low µM, affecting both TTX-S and TTX-R types.</p>Fórmula:C21H29NO3Pureza:98%Cor e Forma:SolidPeso molecular:343.46A778317
CAS:<p>A778317 is a stereoselective, high-affinity antagonist.</p>Fórmula:C23H25N3OPureza:98%Cor e Forma:SolidPeso molecular:359.46AF-2785
CAS:<p>In epididymal epithelial cells, AF-2785 inhibits cystic fibrosis transmembrane conductance regulator Cl(-) channels.</p>Fórmula:C17H12Cl2N2O2Pureza:98%Cor e Forma:SolidPeso molecular:347.2A 80b
CAS:<p>A-80b: synthetic pyridazinoindole; potent, lasting antihypertensive; lowers diastolic more; no change in heart rate; inhibits Ca2+-induced contraction.</p>Fórmula:C16H17N7Pureza:98%Cor e Forma:SolidPeso molecular:307.35ABP-700
CAS:<p>ABP-700 is a positive allosteric modulator of the GABAA receptor.</p>Fórmula:C17H18N2O4Pureza:98%Cor e Forma:SolidPeso molecular:314.34NS4591
CAS:<p>NS4591 is a modulator of SK-IK channels.</p>Fórmula:C11H12Cl2N2OPureza:98%Cor e Forma:SolidPeso molecular:259.13NMDA receptor modulator 5
CAS:<p>NMDA receptor modulator 5 (Compound 195), a potent NMDA receptor modulator, exhibits potential for neurological disorder research [1].</p>Fórmula:C14H11F3N2O3SCor e Forma:SolidPeso molecular:344.31Methsuximide
CAS:Methsuximide is an anticonvulsant agent which appeared to be effective in petit mal, psychomotor and focal motor attacks [1].Fórmula:C12H13NO2Cor e Forma:Crystals From Dilute Alcohol SolidPeso molecular:203.24Carabersat
CAS:<p>Carabersat（SB 204269） is a novel and effective anticonvulsant and antiepileptic agent.</p>Fórmula:C20H20FNO4Pureza:>99.99%Cor e Forma:SolidPeso molecular:357.38ZAPA sulfate
CAS:<p>GABAA receptors agonist</p>Fórmula:C4H8N2O6S2Pureza:98%Cor e Forma:SolidPeso molecular:244.25Synthalin dihydrochloride
CAS:<p>Synthalin dihydrochloride is a channel blocker of K+.</p>Fórmula:C12H30Cl2N6Pureza:98%Cor e Forma:SolidPeso molecular:329.313',4'-Dichlorobenzamil HCl
CAS:<p>3',4'-Dichlorobenzamil HCl is an inhibitor of Na+ transport, Na+/Ca2+ exchanger, sarcoplasmic reticulum Ca2+ release channels.</p>Fórmula:C13H12Cl3N7OPureza:98%Cor e Forma:Yellow SolidPeso molecular:388.64BAY-Y-5959
CAS:<p>BAY-Y-5959, a calcium channel agonist, is used potentially for the treatment of arrhythmia, heart failure and myocardial.</p>Fórmula:C26H24N4O2Cor e Forma:SolidPeso molecular:424.49VU0183254
CAS:<p>VU0183254, an insect OR agonist, inhibits odor-driven OR complex activation by targeting the Orco subunit.</p>Fórmula:C22H18N4O2S2Pureza:98%Cor e Forma:SolidPeso molecular:434.53AHR-9294
CAS:<p>AHR-9294 is a novel inhibitor of H, K-ATPase. It also antagonizes gastric HCl secretion in vivo.</p>Fórmula:C22H24N2O3Cor e Forma:SolidPeso molecular:364.44NSC103054
CAS:<p>NSC103054 is an ABCG2 transporter function inhibitor.</p>Fórmula:C18H22Br2O2Pureza:98%Cor e Forma:SolidPeso molecular:430.17AHR-10718
CAS:<p>AHR-10718 has an antiarrhythmic effect.</p>Fórmula:C22H35N3O7SPureza:98%Cor e Forma:SolidPeso molecular:485.6SOCE inhibitor 1
CAS:<p>SOCE inhibitor 1 is a inhibitor of store-operated calcium entry (SOCE)(IC50 of 4.4 μM).</p>Fórmula:C25H22F3N5O4Pureza:98%Cor e Forma:SolidPeso molecular:513.47(RS)-3,4-DCPG
CAS:<p>antagonist of AMPA receptors and agonist of mGluR8</p>Fórmula:C10H9NO6Pureza:98%Cor e Forma:SolidPeso molecular:239.18Lubeluzole
CAS:<p>Lubeluzole, a well-known neuroprotective agent, is recently proved useful to potentiate the activity of anti-cancer drugs.</p>Fórmula:C22H25F2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:433.51HENA
CAS:<p>HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.</p>Fórmula:C30H48NaO3Pureza:98%Cor e Forma:SolidPeso molecular:479.701NMDA receptor potentiator-1
CAS:<p>Compound 1368 is a selective NMDA receptor enhancer; IC50s: 4 μM for NR2C, 5 μM for NR2D.</p>Fórmula:C26H26ClNO5Cor e Forma:SolidPeso molecular:467.94KC 12291 hydrochloride
CAS:<p>voltage-gated sodium channel blocker</p>Fórmula:C22H28ClN3O3SPureza:98%Cor e Forma:SolidPeso molecular:449.99Lanceotoxin A
CAS:<p>Lanceotoxin A is a potent Ip blocker.</p>Fórmula:C32H44O12Pureza:98%Cor e Forma:SolidPeso molecular:620.68Dopropidil hydrochloride
CAS:<p>Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris.</p>Fórmula:C20H36ClNO2Cor e Forma:SolidPeso molecular:357.96MPO-IN-5
CAS:<p>MPO-IN-5: strong, irreversible MPO blocker; IC50s: 0.22 μM for peroxidation, 2.8 μM for hERG.</p>Fórmula:C24H24N6O2Cor e Forma:SolidPeso molecular:428.49SCH00013
CAS:<p>SCH00013 is a cardiotonic that enhances myofibrillar Ca++ sensitivity, with notable effects at pH 7.2-7.4.</p>Fórmula:C18H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:324.38GZ4
CAS:<p>GZ4 is a Ca2+ currents inhibitor, acting on cell surface channels.</p>Fórmula:C11H17NO2Pureza:98%Cor e Forma:SolidPeso molecular:195.26AFD-21
CAS:<p>AFD-21 is a class I antiarrhythmic that inhibits sodium channels with moderate kinetics.</p>Fórmula:C28H39NO5Pureza:98%Cor e Forma:SolidPeso molecular:469.61Hexadecylphosphoserine
CAS:<p>Hexadecylphosphoserine is a representative growth inhibitor.</p>Fórmula:C19H40NO6PPureza:98%Cor e Forma:SolidPeso molecular:409.54-(Phenyldiazenyl)benzoic acid
CAS:<p>4-(Phenyldiazenyl)benzoic acid is a photosensitive and photoswitchable TRPA1 agonist that can be used as pharmacological tool to study pain signaling.</p>Fórmula:C13H10N2O2Cor e Forma:SolidPeso molecular:226.23Metaphit
CAS:<p>Acylator of PCP and σ-receptors</p>Fórmula:C18H24N2SPureza:98%Cor e Forma:SolidPeso molecular:300.46(S)-Baclofen
CAS:<p>(S)-Baclofen may treat hyperacusis and tinnitus by reducing auditory pathway excitation.</p>Fórmula:C10H12ClNO2Pureza:98%Cor e Forma:SolidPeso molecular:213.66AMG7905
CAS:<p>AMG7905 is a modulator of transient receptor potential vanilloid type 1.</p>Fórmula:C25H24F3N5SPureza:98%Cor e Forma:SolidPeso molecular:483.55Ro18-5362
CAS:<p>Ro18-5362 is the less active prodrug of Ro 18-5364.</p>Fórmula:C22H25N3O2SPureza:98%Cor e Forma:SolidPeso molecular:395.52Ceefourin-2
CAS:<p>Ceefourin-2 is a highly selective multidrug resistance protein 4 inhibitor.</p>Fórmula:C15H9ClF3N3O2Pureza:98%Cor e Forma:SolidPeso molecular:355.7BDF 9148
CAS:<p>BDF 9148, a Na(+)-channel modulator, increases the contractile force of guinea-pig atria and papillary muscles.</p>Fórmula:C28H27N3O3Pureza:98%Cor e Forma:SolidPeso molecular:453.53JTV-519 fumarate
CAS:<p>Ryanodine receptor (RyR) inhibitor; stabilizes RyR2 in a closed conformation. Exhibits antiarrhythmic and cardioprotective properties in vivo.</p>Fórmula:C29H36N2O6SCor e Forma:SolidPeso molecular:540.67EO-122
CAS:<p>EO-122, a calcium channel antagonist and sodium channel antagonist, is used potentially for the treatment of arrhythmia.</p>Fórmula:C16H23ClN2OCor e Forma:SolidPeso molecular:294.82DAA-1097
CAS:<p>DAA-1097 is a novel ligand of peripheral benzodiazepine receptor.</p>Fórmula:C24H24ClNO3Pureza:98%Cor e Forma:SolidPeso molecular:409.91Levamlodipine gentisate
CAS:<p>Levamlodipine gentisate, an active amlodipine enantiomer, is a dihydropyridine calcium channel blocker for treating hypertension and angina.</p>Fórmula:C27H31ClN2O9Pureza:98%Cor e Forma:SolidPeso molecular:563JTT-552
CAS:<p>JTT-552, a uric acid transporter 1 (URAT1) inhibitor, is used potentially for the treatment of hyperuricemia.</p>Fórmula:C15H12ClNO3Pureza:98%Cor e Forma:SolidPeso molecular:289.71TRPC5-IN-1
CAS:<p>TRPC5-IN-1 is a TRPC5 inhibitor active in various animal models of chronic kidney disease.</p>Fórmula:C20H16N4OCor e Forma:SolidPeso molecular:328.37(S)-3-Carboxy-4-hydroxyphenylglycine
CAS:<p>group I metabotropic glutamate receptor antagonist and group II mGlu agonist</p>Fórmula:C9H9NO5Pureza:98%Cor e Forma:SolidPeso molecular:211.17PNU 37883 hydrochloride
CAS:<p>Kir6 (KATP) channel antagonist</p>Fórmula:C21H36ClN3OPureza:98%Cor e Forma:SolidPeso molecular:381.98TAS-4
CAS:<p>TAS-4 is a modulator of metabotropic glutamate receptor 4-positive allosteric.</p>Fórmula:C12H8Cl2N2OPureza:98%Cor e Forma:SolidPeso molecular:267.11N20C hydrochloride
CAS:<p>N20C hydrochloride (2-((3,3-diphenylpropyl)amino)acetamide hydrochloride) is a non-competitive NMDA receptor open-channel blocker.</p>Fórmula:C17H21ClN2OPureza:99.9%Cor e Forma:SolidPeso molecular:304.81Hydroflumethiazide
CAS:<p>Hydroflumethiazide is a thiazide diuretic. It has also shown the activity of anti-hypertensive.</p>Fórmula:C8H8F3N3O4S2Cor e Forma:Crystals SolidPeso molecular:331.29Gea 857
CAS:<p>Gea 857 is a potassium conductance putative blocker.</p>Fórmula:C15H22ClNO2Pureza:98%Cor e Forma:SolidPeso molecular:283.79Lombazole
CAS:<p>Lombazole is an antimicrobial agent in the class of imidazole.</p>Fórmula:C22H17ClN2Cor e Forma:SolidPeso molecular:344.84D-3263
CAS:<p>D-3263 is an agonist of transient receptor potential melatonin member 8 (TRPM8) with potential antitumor activity.</p>Fórmula:C21H31N3O3Pureza:98%Cor e Forma:SolidPeso molecular:373.49TB 21007
CAS:<p>GABAA receptor inverse agonist</p>Fórmula:C15H17NO2S3Pureza:98%Cor e Forma:SolidPeso molecular:339.5Aladorian
CAS:<p>Aladorian (ARM036), a benzothiazepine, has anti-arrhythmic properties for heart failure and CPVT research.</p>Fórmula:C12H13NO4SPureza:98%Cor e Forma:SolidPeso molecular: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>Fórmula:C11H21N5O3Cor e Forma:SolidPeso molecular:271.32GSK-5498A
CAS:<p>GSK-5498A: Selective CARC blocker, inhibits release of mediators from mast cells and cytokines from T-cells (IC50, 1 μM).</p>Fórmula:C18H11F6N3OCor e Forma:SolidPeso molecular:399.29Ro 8-4304
CAS:<p>Ro 8-4304 Hydrochloride is an antagonist of NMDA receptor with IC50 of 0.4 μM</p>Fórmula:C21H23FN2O3Pureza:98%Cor e Forma:SolidPeso molecular:370.42GABAA receptor agent 6
CAS:<p>GABAA receptor agent 6 (compound 2027) is a potent γ-GABAAR antagonist with low cellular membrane permeability (Ki = 0.56 μM) [1].</p>Fórmula:C18H25N3O2Cor e Forma:SolidPeso molecular:315.41AMG8788
CAS:<p>AMG8788 is a selective, potent and orally active TRPM8 antagonist (IC50: 63.2 nM).</p>Fórmula:C23H18F4N2OCor e Forma:SolidPeso molecular:414.4CS476
CAS:<p>CS476 is a potent drug of hypoglycaemic.</p>Fórmula:C24H29N3O5SPureza:98%Cor e Forma:SolidPeso molecular:471.57Fluzinamide
CAS:<p>Fluzinamide (AHR-8559) has anticonvulsant effects on ignited amygdala seizures.</p>Fórmula:C12H13F3N2O2Pureza:99.38% - >99.99%Cor e Forma:SolidPeso molecular:274.24Laurinterol
CAS:<p>Laurinterol is an antimicrobial from the marine alga Laurencia okamurai.</p>Fórmula:C15H19BrOCor e Forma:SolidPeso molecular:295.21BRL 55834
CAS:<p>BRL 55834, a potassium channel activator, has shown to relax airways and vasculature in vivo.</p>Fórmula:C18H20F5NO3Pureza:98%Cor e Forma:SolidPeso molecular: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>Fórmula:C20H22N2O4SPureza:98%Cor e Forma:SolidPeso molecular:386.46FG8119
CAS:<p>FG8119 is a novel benzodiazepine agonist with potential anticonvulsant and antiepileptic activity for the study of neurological disorders.</p>Fórmula:C17H15N5O2Pureza:>99.99%Cor e Forma:SolidPeso molecular:321.33PF-05214030
CAS:<p>PF-05214030 is a novel potent TRPV4 antagonist (hTRPV4 IC50 4nM; rTRPV4 IC50 27nM).</p>Fórmula:C17H13Cl2FN2O4SCor e Forma:SolidPeso molecular:431.27(RS)-CPP
CAS:<p>(RS)-CPP is a NMDA antagonist.</p>Fórmula:C8H17N2O5PPureza:98%Cor e Forma:SolidPeso molecular:252.2V116517
CAS:<p>V-116517, a TRPV1 antagonist, is used potentially for the treatment of severe pain due to osteoarthritis and chronic pain due postherpetic neuralgia (PHN).</p>Fórmula:C19H18ClF3N4O3Cor e Forma:SolidPeso molecular:442.82Quinine hemisulfate
CAS:<p>Quinidine: antiarrhythmic, orally active, inhibits cytochrome P450db, blocks K+ channels (IC50: 19.9μM), may aid in malaria research.</p>Fórmula:C40H50N4O8SPureza:98%Cor e Forma:SolidPeso molecular:746.92Niguldipine 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>Fórmula:C36H39N3O6Pureza:98.97%Cor e Forma:SolidPeso molecular:609.71CGP 28392
CAS:<p>CGP 28392 is used as a partial calcium channel agonist.</p>Fórmula:C18H17F2NO5Pureza:98%Cor e Forma:SolidPeso molecular:365.33Almokalant
CAS:<p>Almokalant: Class III antiarrhythmic, K+ channel blocker, inhibits Ikr current.</p>Fórmula:C18H28N2O3SPureza:98%Cor e Forma:SolidPeso molecular:352.49UT-B-IN-1
CAS:<p>UT-B-IN-1: reversible UT-B inhibitor, IC50: 10 nM (human), 25 nM (mouse), low toxicity, diuretic research tool.</p>Fórmula:C20H17N5O2S3Cor e Forma:SolidPeso molecular:455.58RH01617
CAS:<p>RH01617 possesses potent inhibitory activities against Kv1.5.</p>Fórmula:C22H26N2O5SPureza:98%Cor e Forma:SolidPeso molecular:430.52GSK-5503A
CAS:<p>GSK-5503A is a novel channel blocker of CRAC.</p>Fórmula:C23H17F2N3O2Pureza:98%Cor e Forma:SolidPeso molecular:405.4Glypromate
CAS:<p>Glypromate (Gly-Pro-Glu) is a neuroprotective agent, is a weak NMDA receptor agonist</p>Fórmula:C12H19N3O6Pureza:98%Cor e Forma:SolidPeso molecular:301.3D-AP4
CAS:<p>broad spectrum excitatory amino acid receptor antagonist</p>Fórmula:C4H10NO5PPureza:98%Cor e Forma:White PowderPeso molecular:183.1SR57227A
CAS:<p>SR 57227A: Selective 5-HT3 receptor inhibitor, affects NMDA responses, has anti-depressant effects and reduces aggression in rats.</p>Fórmula:C10H14ClN3Pureza:98%Cor e Forma:SolidPeso molecular:211.69L-701252
CAS:<p>L-701252, a potent glycine site NMDA receptor antagonist, exhibits an inhibition concentration (IC50) of 420 nM.</p>Fórmula:C13H10ClNO3Pureza:97.7%Cor e Forma:White Crystalline SolidPeso molecular:263.68PNU-107484A
CAS:<p>PNU-107484A is a unique GABA(A) receptor ligand.</p>Fórmula:C18H23ClN6Pureza:98%Cor e Forma:SolidPeso molecular:358.87LY 233536
CAS:<p>LY 233536 is a novel, competitive antagonist of NMDA receptor.</p>Fórmula:C12H19N5O2Pureza:98%Cor e Forma:SolidPeso molecular:265.31BK 129
CAS:BK 129 is a local anesthetic with relaxant properties. BK 129 inhibits Ca2+ entry into the smooth muscle cell and Ca2+ release from sarcoplasmic reticulum.Fórmula:C22H36N2O4Pureza:98%Cor e Forma:SolidPeso molecular:392.53H100
CAS:<p>H100 inhibits Cl- transport, mildly affects NaK2Cl cotransporter and Band 3 anion exchanger, not KCl cotransporter.</p>Fórmula:C18H16N2O6SPureza:98%Cor e Forma:SolidPeso molecular:388.4Dicirenone
CAS:<p>Dicirenone (SC26304) inhibits the Mineralocorticoid receptor (MR), aldosterone regulation of the urinary K+:Na+ ratio, and aldosterone binding to renal</p>Fórmula:C26H36O5Pureza:99.1%Cor e Forma:SolidPeso molecular:428.56Guanosine 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).Fórmula:C18H37N7O17P2Peso molecular:685.47KMUP-4
CAS:<p>Kmup-4 is an enhancer of cGMP activity and an aortic smooth muscle relaxant.</p>Fórmula:C19H23N7O4Cor e Forma:SolidPeso molecular:413.43GSK1702934A
CAS:<p>GSK1702934A is a TRPC3 agonist with pro-arrhythmic and positive inotropic effects and is used in the study of diabetes mellitus.</p>Fórmula:C22H25N3O2SPureza:98.15%Cor e Forma:SolidPeso molecular:395.52Eltanexor Z-isomer
CAS:<p>Eltanexor Z-isomer, less active than KPT-8602, inhibits Z138, MM1S, and 3T3 cells with IC50s: 100 nM-50 μM, <100 nM, >30 μM.</p>Fórmula:C17H10F6N6OCor e Forma:SolidPeso molecular:428.29N-Oleoyl Valine
CAS:N-Oleoyl valine, an N-acyl amine, antagonizes TRPV3 for thermoregulation; rises post-cold exposure; elevates in mouse lung injury.Fórmula:C23H43NO3Peso molecular: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>Fórmula:C15H23N5O2SPureza:99.92%Cor e Forma:SolidPeso molecular:337.443-Chlorodiphenylamine
CAS:3-Cl-DPA, a cardiac troponin activator, acts by a mechanism distinct from bepridil or TFP.Fórmula:C12H10ClNCor e Forma:SolidPeso molecular:203.67SM-6586
CAS:<p>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 cerebrovascular</p>Fórmula:C26H27N5O5Pureza:99.43%Cor e Forma:SolidPeso molecular:489.52(5R)-BW-4030W92
CAS:<p>(5R)-BW-4030W92 is the R-type of BW-4030W92, the active enantiomer.</p>Fórmula:C11H9Cl2FN4Pureza:98.27%Cor e Forma:SolidPeso molecular:287.12NHE3-IN-3
CAS:<p>NHE3-IN-3 inhibits human/rat NHE3 with pIC50s 6.2/6.6; 98% oral bioavailability in rats.</p>Fórmula:C16H16Cl2N2O2SCor e Forma:SolidPeso molecular:371.28Bamaluzole
CAS:<p>Bamaluzole is an agonist of GABA receptor.</p>Fórmula:C14H12ClN3OPureza:98%Cor e Forma:SolidPeso molecular:273.72UBP141
CAS:<p>UBP141 is a antagonist of N-methyl-D-aspartate (NMDA) receptor.</p>Fórmula:C21H18N2O5Pureza:98%Cor e Forma:SolidPeso molecular:378.38Aprindine hydrochloride
CAS:<p>Aprindine HCl, a Class 1b antiarrhythmic, treats heart arrhythmias, outperforming digoxin in delaying atrial fibrillation. It's effective orally.</p>Fórmula:C22H31ClN2Cor e Forma:SolidPeso molecular:358.95TC-AQP1-1
CAS:<p>TC-AQP1-1 blocks aquaporin 1; found via virtual screening; hinders water flux in Xenopus oocytes at low µM.</p>Fórmula:C12H10O4Pureza:97.59%Cor e Forma:SolidPeso molecular:218.21GABAA receptor agent 8
CAS:<p>Compound 5e, a GABAA receptor modulator, shows potent anticonvulsant effects with low neurotoxicity for epilepsy research.</p>Fórmula:C19H16N4OCor e Forma:SolidPeso molecular:316.36AM12
CAS:<p>AM12 inhibits Lanthanide-evoked TRPC5 activity (IC50: 0.28 μM).</p>Fórmula:C15H9BrO5Pureza:98%Cor e Forma:SolidPeso molecular:349.13KRP-199
CAS:<p>KRP-199, a highly potent and selective antagonist for the AMPA receptors, exhibits good neuroprotective effects in vivo.</p>Fórmula:C22H14F3N5O7Pureza:98%Cor e Forma:SolidPeso molecular:517.37Nav1.7-IN-2
CAS:<p>Nav1.7-IN-2 is avoltage-gated sodium channels (Nav) inhibitor in particular Nav 1.7(IC50 of 80 nM).</p>Fórmula:C22H22FN5O2Pureza:98%Cor e Forma:SolidPeso molecular:407.44Cilobradine hydrochloride
CAS:<p>Cilobradine hydrochloride (DK-AH 269) is an HCN Channel blocker and an open channel blocker of neuronal Ih and related cardiac If channels.</p>Fórmula:C28H39ClN2O5Pureza:98.40%Cor e Forma:SolidPeso molecular:519.07(S)-(-)-HA 966
CAS:<p>(S)-(-)-HA 966 is a NMDA receptor antagonist.</p>Fórmula:C4H8N2O2Pureza:98%Cor e Forma:SolidPeso molecular:116.12Sodium Channel inhibitor 2
CAS:<p>Sodium Channel inhibitor 2 is a blocker of sodium channel.</p>Fórmula:C26H25Cl2N3OPureza:98%Cor e Forma:SolidPeso molecular:466.4NMDA receptor antagonist 5
CAS:<p>Compound 10e: potent, non-toxic, brain-permeable NMDA receptor antagonist; key for neurological research.</p>Fórmula:C19H16BrNO2Cor e Forma:SolidPeso molecular:370.24Nav1.1 activator 1
CAS:<p>Nav1.1 activator 1 is a highly potent activator of Nav1.1 with BBB penetration.</p>Fórmula:C24H23F3N4OPureza:98%Cor e Forma:SolidPeso molecular:440.46Diproteverine
CAS:<p>Diproteverine is a calcium antagonist, it has antianginal property.</p>Fórmula:C26H35NO4Pureza:98%Cor e Forma:SolidPeso molecular:425.56FSBA hydrochloride
CAS:<p>FSBA hydrochloride(5'-p-Fluorosulfonylbenzoyladenosine) is an ATP analogue serving as an affinity probe for the ATP site of Na/K-ATPase.</p>Fórmula:C17H17ClFN5O7SPureza:97.96%Cor e Forma:SolidPeso molecular:489.86GNE-6901
CAS:<p>GNE-6901 is a selective GluN2A PAM.</p>Fórmula:C18H17FN2O3SCor e Forma:SolidPeso molecular:360.4TC-T 6000
CAS:<p>TC-T 6000 (hENT4-IN-1) is an ENT4 inhibitor with vasodilator activity that inhibits hENT1 and hENT2 for the study of cancer and cardiovascular damage.</p>Fórmula:C26H48N8O2Pureza:98.14%Cor e Forma:SolidPeso molecular:504.71CP-465022 (maleate)
CAS:<p>CP-465022 Maleate: A selective noncompetitive AMPA antagonist with IC50 of 25 nM, showing anticonvulsant effects and useful for AMPA-related studies.</p>Fórmula:C30H28ClFN4O5Cor e Forma:SolidPeso molecular:579.02CGP 36216 hydrochloride
CAS:<p>CGP 36216 hydrochloride is a potent and selective antagonist of GABAB receptors (IC50: 43 μM).</p>Fórmula:C5H14NO2PPureza:98%Cor e Forma:SolidPeso molecular:151.14CP-457920
CAS:<p>CP-457920 is a selective α5 GABAA receptor inverse agonist that is suitable for investigating dementia in Alzheimer's disease.</p>Fórmula:C18H17N3O3Pureza:99.06% - 99.74%Cor e Forma:SolidPeso molecular:323.35ML402
CAS:<p>ML402 (ZINC3671497) is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.</p>Fórmula:C14H14ClNO2SPureza:99.71%Cor e Forma:SolidPeso molecular:295.78ATX-II TFA
<p>ATX-II TFA, a specific Na+ channel modulator toxin, is derived from the venom of the sea anemone (Anemonia sulcata).</p>Pureza:98%Cor e Forma:Odour SolidLemildipine
CAS:<p>Lemildipine is a new blocker of dihydropyridine calcium entry.</p>Fórmula:C20H22Cl2N2O6Cor e Forma:SolidPeso molecular:457.3Zatebradine hydrochloride
CAS:<p>Zatebradine hydrochloride (UL-FS-49CL) inhibits HCN channels (IC50: ~1.9 µM) blocking human HCN1-4 currents effectively.</p>Fórmula:C26H37ClN2O5Pureza:97%Cor e Forma:SolidPeso molecular:493.04Nav1.7 inhibitor
CAS:<p>Nav1.7 inhibitor is a Nav1.7 inhibitor for research in the field of pain and anesthesia.</p>Fórmula:C15H11Cl3FNO4SPureza:97.52%Cor e Forma:SolidPeso molecular:426.68CP-100356 hydrochloride
CAS:<p>CP-100356 hydrochloride is an MDR1 (P-gp) and BCRP inhibitor, a nucleotide-derived substrate analog that induces stomatal opening in the dark.</p>Fórmula:C31H37ClN4O6Pureza:99.19%Cor e Forma:SolidPeso molecular:597.1Cyclic ADP-ribose
CAS:<p>cADPR, made from NAD+, boosts calcium in cells via Ryanodine receptors and TRPM2 channels.</p>Fórmula:C15H21N5O13P2Pureza:98%Cor e Forma:Lyophilized PowderPeso molecular: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>Fórmula:C17H20N2O3Pureza:99.62%Cor e Forma:Solid CrystallinePeso molecular:300.35BMS-919373
CAS:<p>BMS-919373 is a potassium channel Kv1.5 (KCNA5) inhibitor for atrial fibrillation and acute coronary syndrome.</p>Fórmula:C25H20N6O2SPureza:98.51% - 99.01%Cor e Forma:SolidPeso molecular:468.53PKF050-638
CAS:<p>PKF050-638 disrupts CRM1-NES, inhibits HIV-1 Rev export; selective with IC50=0.04 μM.</p>Fórmula:C13H13ClN4O2Pureza:98%Cor e Forma:SolidPeso molecular:292.72Nav1.7-IN-6
CAS:<p>Nav1.7-IN-6, a selective inhibitor of Nav1.7.</p>Fórmula:C25H25ClF6N2O4SPureza:98%Cor e Forma:SolidPeso molecular:598.99Terodiline hydrochloride
CAS:<p>Terodiline hydrochloride is an antagonist of M1-selective muscarinic receptor (mAChR)(Kbs of 15, 160, 280, and 198 nM in rabbit vas deferens (M1), atria (M2),</p>Fórmula:C20H28ClNPureza:98%Cor e Forma:SolidPeso molecular:317.9Istaroxime oxalate
CAS:<p>Istaroxime (PST-2744) is a positive inotrope that inhibits Na+/K+ ATPase, raising intracellular sodium and calcium levels.</p>Fórmula:C23H34N2O7Cor e Forma:SolidPeso molecular:450.53FR-168888 mesylate
CAS:<p>FR-168888, a new Na+/H+ exchange inhibitor, can protect the heart from arrhythmia and myocardial cell death in ischemic and reperfused situations.</p>Fórmula:C14H18N4O5SPureza:98%Cor e Forma:SolidPeso molecular:354.38TRPC6-PAM-C20
CAS:<p>TRPC6-PAM-C20, a selective enhancer for TRPC6, boosts calcium in HEK cells and OAG-related platelet clumping, EC50: 2.37μM.</p>Fórmula:C22H21NO4Pureza:98.16%Cor e Forma:SolidPeso molecular:363.41Nav1.8-IN-2
CAS:<p>Nav1.8-IN-2 (compound 35A) strongly inhibits Nav1.8 (IC50: 0.4 nM), useful for researching pain, cough, and pruritus.</p>Fórmula:C18H13Cl2F3N2O3Cor e Forma:SolidPeso molecular:433.21McN5691
CAS:<p>McN5691 is a voltage sensitive calcium channel blocker.</p>Fórmula:C30H35NO3Pureza:98.93% - 99.38%Cor e Forma:SolidPeso molecular: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>Fórmula:C29H32N2O6SPureza:98.53% - 99.47%Cor e Forma:SolidPeso molecular:536.64Picoprazole
CAS:<p>Picoprazole is a specific H+/K+-ATPase inhibitor (IC50 of 3.1±0.4 μM).</p>Fórmula:C17H17N3O3SPureza:98%Cor e Forma:SolidPeso molecular:343.4Farnesyl pyrophosphate
CAS:<p>Farnesyl pyrophosphate: 15-C isoprenoid, TRPM2 agonist, crucial for cholesterol, ubiquinones, protein farnesylation, and GGPP synthesis.</p>Fórmula:C15H28O7P2Cor e Forma:SolidPeso molecular:382.33(R)-Baclofen hydrochloride
CAS:<p>Arbaclofen HCl, a GABA-B agonist, treats spasticity from spinal injury by reducing excitatory transmission.</p>Fórmula:C10H13Cl2NO2Pureza:98%Cor e Forma:SolidPeso molecular:250.12KRN4884
CAS:<p>KRN 4884 activates KATP channels (EC50=0.55 μM) at 0.1-3 μM with 1 mM ATP.</p>Fórmula:C15H14ClN5Pureza:98%Cor e Forma:SolidPeso molecular:299.76Vernakalant
CAS:<p>Vernakalant (RSD-1235) is a mixed ion channel blocker.</p>Fórmula:C20H31NO4Pureza:98%Cor e Forma:SolidPeso molecular:349.46GABA-AT-IN-1
CAS:<p>GABA-AT-IN-1 (Compound 6) is an inhibitor of γ-aminobutyric acid transaminase (GABA-AT) that crosses the blood-brain barrier.</p>Fórmula:C23H18N2O6Cor e Forma:SolidPeso molecular:418.4CCD-3693
CAS:<p>CCD-3693 is a gamma-aminobutyric acid (GABA) receptor agonist.</p>Fórmula:C21H31F3O2Pureza:98%Cor e Forma:SolidPeso molecular:372.46L-4FPG
CAS:<p>L-4FPG is a Glycine derivative, inhibits the neutral amino acid transporters ASCT1 and ASCT2.</p>Fórmula:C8H8FNO2Pureza:99.26%Cor e Forma:SolidPeso molecular:169.15Amsacrine
CAS:<p>Amsacrine (AMSA) (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.</p>Fórmula:C21H19N3O3SPureza:99.2%Cor e Forma:Yellow Crystalline Powder SolidPeso molecular:393.46CFTR corrector 9
CAS:<p>CFTR corrector 9 is a CF modulator used to research cystic fibrosis and related disorders.</p>Fórmula:C16H14N2O4Pureza:98.24%Cor e Forma:SolidPeso molecular:298.29Nifekalant hydrochloride
CAS:<p>Nifekalant hydrochloride is an IKr potassium channel blocker with an IC50 of 10 µM.</p>Fórmula:C19H28ClN5O5Pureza:99.91%Cor e Forma:SolidPeso molecular:441.91V-9302
CAS:<p>V-9302 (V9302) is a competitive antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 (IC50: 9.6 uM</p>Fórmula:C34H38N2O4Pureza:98% - 99.54%Cor e Forma:SolidPeso molecular:538.68Benzamil hydrochloride
CAS:<p>Benzamil hydrochloride is a specific and potent sodium channel (ENaC) blocker.</p>Fórmula:C13H15Cl2N7OPureza:98%Cor e Forma:SolidPeso molecular:356.21Homoquinolinic acid
CAS:<p>NMDA receptor agonist</p>Fórmula:C8H7NO4Pureza:98%Cor e Forma:SolidPeso molecular:181.15SCH 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>Fórmula:C8H15NO3Pureza:98%Cor e Forma:SolidPeso molecular:173.21Abeprazan
CAS:<p>Abeprazan is a potassium-competitive acid blocker targeting acid-related diseases without acid activation.</p>Fórmula:C19H17F3N2O3SPureza:98%Cor e Forma:SolidPeso molecular:410.41ICA
CAS:<p>ICA (N-[4-(2-Pyridinyl)-2-thiazolyl]-2-pyridinamine) is a SK channel inhibitor and exhibits antileishmanial activity (IC50: 2.1 µM).</p>Fórmula:C13H10N4SPureza:99.68%Cor e Forma:SolidPeso molecular:254.31LY339434
CAS:<p>LY339434 is a potent and selective agonist of the kainate receptor GluK1, GluR5.</p>Fórmula:C18H19NO4Pureza:98%Cor e Forma:SolidPeso molecular:313.35Sabiporide
CAS:<p>Sabiporide is a NHE-1 inhibitor and a cardioprotective agent.</p>Fórmula:C18H20ClF3N6O2Cor e Forma:SolidPeso molecular:444.84Biricodar dicitrate
CAS:<p>Biricodar dicitrate (VX-710) is a potent MDR inhibitor with no anticancer activity and can be used to study prostate cancer.</p>Fórmula:C46H57N3O21Pureza:97.78% - 99.78%Cor e Forma:SolidPeso molecular:987.95Ro 25-6981 HCl
CAS:<p>Ro 25-6981 HCl is an effective and selective NMDA glutamate receptors containing the NR2B subunit antagonist.</p>Fórmula:C22H30ClNO2Pureza:98%Cor e Forma:SolidPeso molecular:375.93RH 3421
CAS:<p>RH 3421 is used as a neuroactive dihydropyrazole insecticide.</p>Fórmula:C20H17ClF3N3O3Pureza:98%Cor e Forma:SolidPeso molecular:439.82Phenamil
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>Fórmula:C12H12ClN7OPureza:99.07%Cor e Forma:SolidPeso molecular: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>Fórmula:C19H24N6O2Pureza:99.82%Cor e Forma:SolidPeso molecular:368.43WX-081
CAS:<p>WX-081 is an anti-TB drug effective against DS-TB (MIC: 0.083 μg/ml) and MDR-TB strains (MIC: 0.11 μg/ml) with hERG inhibition (IC50: 1.89 μM).</p>Fórmula:C34H33ClN2O2Cor e Forma:SolidPeso molecular:537.09CM-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>Fórmula:C16H17ClN6O2Pureza:99.94%Cor e Forma:SolidPeso molecular:360.8YM 244769 hydrochloride
CAS:<p>inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)</p>Fórmula:C26H23ClFN3O3Pureza:98%Cor e Forma:SolidPeso molecular:479.93Ro 8-4304 hydrochloride
CAS:<p>Ro 8-4304 hydrochloride is a NMDA receptor antagonist.</p>Fórmula:C21H24ClFN2O3Pureza:98%Cor e Forma:SolidPeso molecular:406.88ZD-9379
CAS:<p>ZD-9379 is a NMDA receptor antagonist.</p>Fórmula:C19H14ClN3O4Pureza:98%Cor e Forma:SolidPeso molecular:383.79UBP714
CAS:<p>UBP714, derived from UBP608, boosts NMDAR in CA1 hippocampus, promising for schizophrenia and cognitive deficits treatment.</p>Fórmula:C11H7BrO4Pureza:98%Cor e Forma:SolidPeso molecular:283.07TTA-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>Fórmula:C20H15ClF3N3OPureza:99.97%Cor e Forma:SolidPeso molecular: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>Fórmula:C23H48NO7PPureza:98%Cor e Forma:SolidPeso molecular: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>Fórmula:C26H36N4O4Pureza:98%Cor e Forma:SolidPeso molecular:468.59UCL-1848 trifluoroacetate salt
CAS:<p>UCL-1848 trifluoroacetate salt is a selective Ca2+-activated, SK potassium channel blocker.</p>Fórmula:C32H34F6N4O4Pureza:98%Cor e Forma:SolidPeso molecular:652.638E2730
CAS:<p>E2730 is a non-competitive GABA transporter 1 (GAT1) inhibitor with anti-epileptic activity, useful in studying neurological disorders.</p>Fórmula:C9H8F4N2O2SPureza:98.22% - 98.54%Cor e Forma:SolidPeso molecular: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>Fórmula:C20H29F3N2O2Pureza:98%Cor e Forma:SolidPeso molecular:386.45
