Canal de calcio
Los canales de calcio son proteínas de membrana que regulan el flujo de iones de calcio hacia dentro y fuera de las células, lo cual es esencial para diversas funciones celulares, como la contracción muscular, la liberación de neurotransmisores y la expresión génica. La desregulación de la actividad de los canales de calcio está asociada con condiciones como la hipertensión, las arritmias cardíacas y los trastornos neurológicos. En CymitQuimica, ofrecemos una amplia selección de moduladores de canales de calcio para apoyar su investigación en salud cardiovascular, neurobiología y transducción de señales.
Se han encontrado 493 productos de "Canal de calcio"
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Argireline
CAS:<p>Argireline (Acetyl hexapeptide-3) is a peptide that inhibits neurotransmitter release, reducing wrinkles.</p>Fórmula:C34H60N14O12SPureza:96.79% - 99.65%Forma y color:White PowderPeso molecular:888.99Propiverine hydrochloride
CAS:<p>Propiverine is a widely used antimuscarinic drug with a mixed mode of action in the treatment of symptoms associated with overactive bladder (OAB).</p>Fórmula:C23H30ClNO3Pureza:99.93%Forma y color:White Crystalling PowerPeso molecular:403.94Praeruptorin E
CAS:<p>Praeruptorin C/E relaxes arteries, reduces heart contractility, acting like calcium blockers. D/E protect mice from acid lung injury by halting PMNs and IL-6.</p>Fórmula:C24H28O7Pureza:98.04% - 99.95%Forma y color:SolidPeso molecular:428.47SR33805
CAS:<p>SR33805 is a potent antagonist of Ca2+ channel(EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively)</p>Fórmula:C32H40N2O5SPureza:99.15%Forma y color:SolidPeso molecular:564.74Lomerizine dihydrochloride
CAS:<p>Lomerizine dihydrochloride (KB-2796) is an antagonist of L- and T-type voltage-gated calcium channels used to treat migraine.</p>Fórmula:C27H30F2N2O3·2HClPureza:99.26% - 99.80%Forma y color:Colourless Crystalline SolidPeso molecular:541.46L-Phenylalanine
CAS:<p>L-Phenylalanine (3-Phenyl-L-alanine) is an essential amino acid and the precursor of the amino acid tyrosine, acts as an antagonist at α2δ calcium channels.</p>Fórmula:C9H11NO2Pureza:99.37% - 99.87%Forma y color:Solid CrystallinePeso molecular:165.19Bepridil hydrochloride
CAS:<p>Bepridil hydrochloride (CERM 1978) is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX), sodium channels and cardiac sarcolemmal KATP channels</p>Fórmula:C24H35ClN2OPureza:99.45% - 99.68%Forma y color:SolidPeso molecular:403Azumolene
CAS:<p>Azumolene (EU4093 free base)</p>Fórmula:C13H9BrN4O3Pureza:98.1% - 98.35%Forma y color:SolidPeso molecular:349.14NFAT Inhibitor-2
CAS:<p>NFAT Inhibitor-2 is a compound used as a molecular building block.</p>Fórmula:C22H20F2N2O4SPureza:97.37%Forma y color:SolidPeso molecular:446.47Dantrolene sodium hemiheptahydrate
CAS:<p>Dantrolene depresses excitation-contraction coupling in skeletal muscle by binding to the ryanodine receptor 1 and decreasing intracellular calcium</p>Fórmula:C14H9N4NaO5·5H2OPureza:99.72%Forma y color:Orange PowderPeso molecular:399.29Ethacrynic acid
CAS:<p>Ethacrynic acid (Edecrin) 是谷胱甘肽 S-转移酶抑制剂，也是NF-κB 信号传导途径的有效抑制剂，并且还调节白三烯的形成。它还可抑制 L 型电压依赖性和储存操作的钙通道，从而导致气道平滑肌细胞松弛。它是利尿剂，具有抗炎特性，可减轻类维生素 A 诱导的小鼠耳部水肿。</p>Fórmula:C13H12Cl2O4Pureza:98.61% - 99.85%Forma y color:Crystals Physical Description White Solid (Ntp 1992)Peso molecular:303.14Gabapentin hydrochloride
CAS:<p>Gabapentin hydrochloride (Neurontin HCl) is a GABA analogue, used to treat seizures and neuropathic pain.</p>Fórmula:C9H17NO2·HClPureza:99.71%Forma y color:Off-White SolidPeso molecular:207.7NS-638
CAS:<p>NS-638 is a Ca2+-channel blocker. It can block K+-stimulated intracellular Ca2+-elevation (IC50: 3.4 μM).</p>Fórmula:C15H11ClF3N3Pureza:98.44%Forma y color:SolidPeso molecular:325.72Cycleanine
CAS:<p>Cycleanine has potent antibacterial, antifungal, antiplasmodial, and cytotoxic activities.</p>Fórmula:C38H42N2O6Pureza:98.04% - 99.57%Forma y color:SolidPeso molecular:622.75Pranidipine
CAS:<p>Pranidipine (OPC-13340) is a novel, long-acting 1,4-dihydropyridine calcium channel blocker.</p>Fórmula:C25H24N2O6Pureza:99.95%Forma y color:Yellow SolidPeso molecular:448.47Glaucine
CAS:<p>Glaucine: antitussive, antioxidative, antiviral, may fight arthritis, boosts IL-10, hinders breast cancer cell spread by inhibiting MMP-9 and NF-κB.</p>Fórmula:C21H25NO4Pureza:99.42% - 99.56%Forma y color:SolidPeso molecular:355.43FPL64176
CAS:<p>FPL64176 is a L-type calcium channels activator.</p>Fórmula:C22H21NO3Pureza:98.68%Forma y color:SolidPeso molecular:347.41Aranidipine
CAS:<p>Aranidipine (MPC1304) (MPC1304) is a calcium channel antagonist with potent and long-lasting antihypertensive effects.</p>Fórmula:C19H20N2O7Pureza:99.15%Forma y color:SolidPeso molecular:388.37TTA-A2
CAS:<p>TTA-A2: T-type calcium channel blocker; anticonvulsant targeting Cav3.1, Cav3.2; IC50 of 89/92 nM; potential for treating neurological conditions.</p>Fórmula:C20H21F3N2O2Pureza:99.5% - 99.9%Forma y color:SolidPeso molecular:378.39Gomisin J
CAS:<p>Gomisin J is a natural product and have vasodilatory activity.</p>Fórmula:C22H28O6Pureza:99.59% - 99.60%Forma y color:SolidPeso molecular:388.45Fantofarone
CAS:<p>Fantofarone (SR 33557) is a highly potent antagonist of Calcium Channel.</p>Fórmula:C31H38N2O5SPureza:96.13% - 99.19%Forma y color:SolidPeso molecular:550.71Fasudil hydrochloride
CAS:<p>Fasudil hydrochloride (HA-1077) is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Ki of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.</p>Fórmula:C14H18ClN3O2SPureza:99.54% - ≥95%Forma y color:White SolidPeso molecular:327.83Ziconotide Acetate (107452-89-1 free base)
CAS:<p>Ziconotide Acetate (Prialt, 107452-89-1) is an analgesic for neuropathic pain, acting on N-type calcium channels to block pain signals.</p>Fórmula:C102H172N36O32S7Pureza:99.52% - 99.87%Forma y color:SolidPeso molecular:2639.2Norfluoxetine Hydrochloride
CAS:<p>Norfluoxetine Hydrochloride (Norfluoxetine HCl) is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.</p>Fórmula:C16H17ClF3NOPureza:99.71%Forma y color:SolidPeso molecular:331.76Lanthanum(III) chloride heptahydrate
CAS:<p>Lanthanum(III) chloride blocks divalent cation channels, useful for biochemical research.</p>Fórmula:Cl3H14LaO7Pureza:98%Forma y color:White Solid PowderPeso molecular:371.37Almorexant
CAS:<p>Almorexant (ACT 078573), a strong dual orexin receptor antagonist, has Ki of 1.3 nM for OX1 and 0.17 nM for OX2.</p>Fórmula:C29H31F3N2O3Pureza:97.75% - 98.02%Forma y color:SolidPeso molecular:512.56Barnidipine hydrochloride
CAS:<p>Barnidipine HCl is a potent dihydropyridine Ca²⁺ blocker with 0.35 nM IC50 in pig coronary artery.</p>Fórmula:C27H30ClN3O6Pureza:99.88%Forma y color:SolidPeso molecular:528(±)-Praeruptorin A
CAS:<p>(±)-Praeruptorin A could exhibit its anti-osteoclastogenic activity by inhibiting p38/Akt-c-Fos-NFATc1 signaling and PLCγ-independent Ca(2+) oscillation.</p>Fórmula:C21H22O7Pureza:98.9% - 99.73%Forma y color:SolidPeso molecular:386.4Manidipine
CAS:<p>Manidipine (Iperten), a calcium channel blocker, which is dihydropyridine type. It is utilized</p>Fórmula:C35H38N4O6Pureza:99.30%Forma y color:SolidPeso molecular:610.7ISX-9
CAS:<p>ISX-9 (Isoxazole 9) is necessary to activate neuron-specific genes as neurogenesis inducer.</p>Fórmula:C11H10N2O2SPureza:97.81% - ≥95%Forma y color:SolidPeso molecular:234.27YM-58483
CAS:<p>YM-58483 (BTP2) is a specific and effective inhibitor of CRAC channels and subsequent Ca2+ signals.</p>Fórmula:C15H9F6N5OSPureza:99.33% - 99.64%Forma y color:SolidPeso molecular:421.32Z944
CAS:<p>Z944 is a T-type calcium channel blocker.</p>Fórmula:C19H27ClFN3O2Pureza:99.8%Forma y color:SolidPeso molecular:383.89Barnidipine
CAS:<p>Barnidipine (YM-09730-5(Free base)) is a calcium channel blocker.</p>Fórmula:C27H29N3O6Pureza:99.98%Forma y color:SolidPeso molecular:491.54Ginsenoside Rf
CAS:<p>Ginsenoside Rf (Panaxoside Rf) is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.</p>Fórmula:C42H72O14Pureza:99.82%Forma y color:SolidPeso molecular:801.01Urolithin C
CAS:<p>Urolithin C is a gut metabolite of ellagic acid. Urolithin C induces apoptosis in PC12 cells through a mitochondria-mediated pathway.</p>Fórmula:C13H8O5Pureza:98.01% - 99.53%Forma y color:SolidPeso molecular:244.2Ginsenoside Ro
CAS:<p>Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist with</p>Fórmula:C48H76O19Pureza:98% - 99.66%Forma y color:SolidPeso molecular:957.11Isradipine
CAS:<p>Isradipine (PN 200-110), a dihydropyridine, is an antihypertensive calcium channel blocker that dilates arteries and reduces resistance.</p>Fórmula:C19H21N3O5Pureza:99.84% - 99.95%Forma y color:Yellow SolidPeso molecular:371.39Ruthenium Red
CAS:<p>Ruthenium Red (Ammoniated ruthenium oxychloride) is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria.</p>Fórmula:Cl6H42N14O2Ru3Pureza:95%Forma y color:Purple PowderPeso molecular:786.34Benidipine hydrochloride
CAS:<p>Benidipine hydrochloride (Coniel) , a hydrochloride salt form of benidipine, is used as a blocker of dihydropyridine calcium channel.</p>Fórmula:C28H32ClN3O6Pureza:99.80%Forma y color:SolidPeso molecular:542.032-Aminoethyl diphenylborinate
CAS:<p>2-Aminoethyl diphenylborinate (2-APB) is a chemical that acts to inhibit both IP3 receptors and TRP channels.</p>Fórmula:C14H16BNOPureza:98.74% - 99.92%Forma y color:WhitePeso molecular:225.09Cyclopiazonic acid
CAS:<p>Cyclopiazonic acid (CPA) is a neurotoxic secondary metabolite (SM) made by A.</p>Fórmula:C20H20N2O3Pureza:99.27% - 99.80%Forma y color:SolidPeso molecular:336.38Ned 19
CAS:<p>Ned 19 inhibits tumor growth, vascularization, lung metastases in mice, and is a selective NAADP antagonist.</p>Fórmula:C30H31FN4O3Pureza:99.66%Forma y color:SolidPeso molecular:514.59Etripamil
CAS:<p>Etripamil is a fast-acting intranasal L-type calcium-channel blocker for Paroxysmal Supraventricular Tachycardia.</p>Fórmula:C27H36N2O4Pureza:99.47% - 99.83%Forma y color:SolidPeso molecular:452.59Levamlodipine besylate
CAS:<p>Levamlodipine besylate, or S-amlodipine (CAS 103129-82-4), is the active enantiomer of amlodipine, used to treat hypertension and angina.</p>Fórmula:C26H31ClN2O8SPureza:99.78% - 99.79%Forma y color:SolidPeso molecular:567.05Dronedarone
CAS:<p>Dronedarone (SR 33589) is an amiodarone analogue which has an effective and promising treatment for Atrial fibrillation.</p>Fórmula:C31H44N2O5SPureza:98.85% - 99.58%Forma y color:SolidPeso molecular:556.76Nicardipine
CAS:<p>Nicardipine (Cardene), a calcium channel blockers belonging to the dihydropyridine class, is a drug used to treat angina and high blood pressure.</p>Fórmula:C26H29N3O6Pureza:99.56%Forma y color:SolidPeso molecular:479.52CDN1163
CAS:<p>CDN1163 is a small molecule activator of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA).</p>Fórmula:C20H20N2O2Pureza:99.83% - ≥95%Forma y color:SolidPeso molecular:320.39Efonidipine
CAS:<p>Efonidipine (NZ-105)(NZ-105) is a dihydropyridine calcium channel blocker, blocking both T-type and L-type calcium channels.</p>Fórmula:C34H38N3O7PPureza:98.35% - 99.47%Forma y color:SolidPeso molecular:631.66OPHIOPOGONIN D
CAS:<p>Ophiopogonin D is a natural product,and is a CYP2J3 inducer that significantly inhibits Ang II induced NF-κB nuclear translocation.</p>Fórmula:C44H70O16Pureza:99.46% - ≥95%Forma y color:SolidPeso molecular:855.02Yangambin
CAS:<p>Yangambin: selective PAF antagonist, hypotensive, inhibits Ca2+ influx, induces peripheral vasodilation, affects CNS.</p>Fórmula:C24H30O8Pureza:98.02%Forma y color:SolidPeso molecular:446.492,5-Di-tert-butylhydroquinone
CAS:<p>2,5-Di-tert-butylhydroquinone (BHQ) is an effective and selective endoplasmic reticulum Ca2+-ATPase inhibitor.</p>Fórmula:C14H22O2Pureza:97.11%Forma y color:PelletslargecrystalsPeso molecular:222.32Taurolithocholic acid sodium salt
CAS:<p>Taurolithocholic acid sodium salt (Sodium taurolithocholate) is the major human metabolite, a bile acid which inhibits radioligand binding to muscarinic M1, but</p>Fórmula:C26H44NNaO5SPureza:99.79% - 99.93%Forma y color:SolidPeso molecular:505.69DHBP dibromide
CAS:<p>DHBP dibromide (1,1'-DI-N-HEPTYL-4,4'-BIPYRIDINIUM DIBRO) is calcium release and a muscle relaxant inhibitor.</p>Fórmula:C24H38Br2N2Pureza:99.73%Forma y color:Yellow To Yellow-Green Powder Or FlakesPeso molecular:514.38Zegocractin
CAS:<p>Zegocractin (CM-4620) is a calcium-release activated calcium-channel (CRAC channel) inhibitor.</p>Fórmula:C19H11ClF3N3O3Pureza:98.82%Forma y color:SolidPeso molecular:421.76MDK-4025
CAS:<p>MDK-4025 is an inhibitor of the high voltage-activated (HVA) Ca2+ current in pyramidal neurons.</p>Fórmula:C19H15ClOPureza:98.65%Forma y color:SolidPeso molecular:294.77Bevantolol hydrochloride
CAS:<p>Bevantolol hydrochloride (NC-1400 hydrochloride) is a β1-adrenoceptor antagonist that treatment angina pectoris and hypertension.</p>Fórmula:C20H28ClNO4Pureza:99.49%Forma y color:SolidPeso molecular:381.9L-Ascorbic acid sodium salt
CAS:<p>L-Ascorbic acid sodium salt (Vitamin C sodium salt) is a more bioavailable form of vitamin C that is an alternative to taking ascorbic acid as a supplement.</p>Fórmula:C6H7NaO6Pureza:98.73% - 99.75%Forma y color:Less Solid PowderPeso molecular:198.11JNJ-26990990
CAS:<p>"JNJ-26990990: broad-spectrum anticonvulsant, less side effects than topiramate, potential for pain and depression treatment; Phase II in 2007."</p>Fórmula:C9H10N2O2S2Pureza:97.37%Forma y color:SolidPeso molecular:242.32Bay K 8644
CAS:<p>Bay K 8644 (SQ 28,873) is a potent, selective activator of L-type Ca2+ channel with IC50 of 17.3 nM.</p>Fórmula:C16H15F3N2O4Pureza:99.41%Forma y color:Yellow PowderPeso molecular:356.3SEA0400
CAS:<p>SEA0400 is a selective inhibitor of the Na+/Ca2+ exchanger.</p>Fórmula:C21H19F2NO3Pureza:98.88% - 99.55%Forma y color:SolidPeso molecular:371.38SN 6
CAS:<p>SN 6 (SN6) is a selective Na+/Ca2+ exchanger (NCX) inhibitor (IC50s of NCX1: 2.9 μM , NCX2: 16 μM ,NCX3: 8.6 μM)</p>Fórmula:C20H22N2O5SPureza:97.28%Forma y color:SolidPeso molecular:402.46Tetrandrine
CAS:<p>Tetrandrine (Sinomenine A) is a naturally occurring biphenylisoquinoline alkaloid, a calcium channel inhibitor. Cost-effective and quality-assured.</p>Fórmula:C38H42N2O6Pureza:99.61% - 99.94%Forma y color:White SolidPeso molecular:622.75Pyridaben
CAS:<p>Pyridaben is a METI acaricide that inhibits mitochondrial electron transport at complex I (METI; Ki = 0.36 nmol/mg protein in rat brain mitochondria).</p>Fórmula:C19H25ClN2OSPureza:97.11% - 99.75%Forma y color:SolidPeso molecular:364.93Equilin
CAS:<p>Equilin (7-Dehydroestrone) is a neurotrophic estrogenic steroid with vasodilatory activity used in the study of hypertension.</p>Fórmula:C18H20O2Pureza:98.57% - 99.72%Peso molecular:268.35Bupivacaine
CAS:<p>Bupivacaine (AH-250) is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels</p>Fórmula:C18H28N2OPureza:99.83%Forma y color:SolidPeso molecular:288.43Amlodipine maleate
CAS:<p>Amlodipine maleate (Amvaz) is an oral dihydropyridine calcium blocker for hypertension and cancer studies.</p>Fórmula:C24H29ClN2O9Pureza:99.4%Forma y color:White To Pale Yellow Crystalline PowderPeso molecular:524.95Apinocaltamide
CAS:<p>Apinocaltamide (ACT-709478) is an orally available and selective T-type calcium channel blocker that cross BBB for Cav3.1, Cav3.2, and Cav3.3,epilepsy.</p>Fórmula:C22H18F3N5OPureza:99.80%Forma y color:SolidPeso molecular:425.41N-Methyl-L-leucin
CAS:<p>N-Methyl-L-leucine ((S)-4-Methyl-2-(methylamino)pentanoic acid) is a novel calcium channel antagonist used in pain research.</p>Fórmula:C7H15NO2Pureza:99.87%Forma y color:SolidPeso molecular:145.2N6-(2-Hydroxyethyl)adenosine
CAS:<p>N6-(2-Hydroxyethyl)adenosine is a sedative, Ca2+ antagonist, and anti-inflammatory, affecting brain and heart blood flow.</p>Fórmula:C12H17N5O5Pureza:99.4%Forma y color:SolidPeso molecular:311.29Diltiazem
CAS:<p>Diltiazem (CRD 401 free base) is an orally available L-type Ca2+ channel blocker with antihypertensive, antiarrhythmic, and cardioprotective properties that prevent post-reperfusion myocardial injury, angina pectoris, and cardiovascular-related diseases.</p>Fórmula:C22H26N2O4SPureza:99.51% - 99.83%Forma y color:White Crystalline Powder SolidPeso molecular:414.52Bupivacaine-d9
CAS:<p>Bupivacaine-d9 is a deuterated compound of Bupivacaine. Bupivacaine has a CAS number of 38396-39-3. Bupivacaine is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.</p>Fórmula:C18H19D9N2OForma y color:SolidPeso molecular:297.48Gabapentin enacarbil
CAS:<p>Gabapentin enacarbil (XP-13512) is a prodrug for the anticonvulsant and analgesic gabapentin, offering sustained dose-proportional exposure and predictable bioavailability.</p>Fórmula:C16H27NO6Pureza:99.31%Forma y color:SolidPeso molecular:329.394-(2-Chlorophenyl)-2-methyl-5-oxo-4,4a,5,7,8,10-hexahydro-1H-pyrido[2',3':2,3]azeto[2,1-c][1,4]oxazine-3-carboxylic Acid
Producto controlado<p>Applications 4-(2-Chlorophenyl)-2-methyl-5-oxo-4,4a,5,7,8,10-hexahydro-1H-pyrido[2',3':2,3]azeto[2,1-c][1,4]oxazine-3-carboxylic Acid is an intermediate in the synthesis of 3-O-Desethyl-5-O-desmethyl Amlodipine (D291305). 3-O-Desethyl-5-O-desmethyl Amlodipine is an impurity of Amlodipine (A633495), which is a dihydropyridine calcium channel blocker.<br>References Arrowsmith, J.E., et al.: J. Med. Chem., 29, 1696 (1986); Burges, R.A., et al.: J. Cardiovasc. Pharmacol., 9, 110 (1987); Haria, M., et al.: Drugs, 50, 560 (1995)<br></p>Fórmula:C17H17ClN2O4Forma y color:NeatPeso molecular:348.7811-tert-Butyl 3-Ethyl 5-methyl 2-((2-((tert-Butoxycarbonyl)amino)ethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-1,3,5(4H)-tricarboxylate
CAS:Producto controlado<p>Applications 1-tert-Butyl 3-Ethyl 5-methyl 2-((2-((tert-Butoxycarbonyl)amino)ethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-1,3,5(4H)-tricarboxylate is an intermediate in the synthesis of 3-O-Desethyl-5-O-desmethyl Amlodipine (D291305). 3-O-Desethyl-5-O-desmethyl Amlodipine is an impurity of Amlodipine (A633495), which is a dihydropyridine calcium channel blocker.<br>References Arrowsmith, J.E., et al.: J. Med. Chem., 29, 1696 (1986); Burges, R.A., et al.: J. Cardiovasc. Pharmacol., 9, 110 (1987); Haria, M., et al.: Drugs, 50, 560 (1995)<br></p>Fórmula:C30H41ClN2O9Forma y color:NeatPeso molecular:609.107Amlodipine hydrochloride
CAS:<p>Amlodipine hydrochloride is a salt of Amlodipine --- a medication used to lower blood pressure and prevent chest pain.</p>Fórmula:C20H26Cl2N2O5Forma y color:SolidPeso molecular:445.34Amlodipine besilate impurity G
CAS:<p>Amlodipine besilate impurity G is a Calcium Channel antagonist with potential application in the study of neurological diseases and is an impurity in the</p>Fórmula:C17H18ClNO4Pureza:98%Forma y color:SolidPeso molecular:335.78Cinepazide
CAS:<p>Cinepazide: a vasodilator targeting adenosine A2 receptors, treats various vascular diseases.</p>Fórmula:C22H31N3O5Forma y color:White PowderPeso molecular:417.5Nifedipine-d6
CAS:<p>Nifedipine D6 is deuterium labeled nifedipine which is a potent blocker of calcium channel.</p>Fórmula:C17H18N2O6Pureza:98%Forma y color:SolidPeso molecular:352.37Cinnarizine D8
CAS:<p>Cinnarizine D8 is a deuterium-labeled Cinnarizine which is an antihistamine and a calcium channel blocker.</p>Fórmula:C26H28N2Pureza:98%Forma y color:SolidPeso molecular:376.573Topiramate D12
CAS:<p>Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.</p>Fórmula:C12H21NO8SPureza:98%Forma y color:SolidPeso molecular:351.44Maresin 1
CAS:<p>Maresin 1 is biosynthesized by macrophages (MΦ) and possesses significant anti-inflammatory activity that attenuates LPS-induced lung injury in mice.</p>Fórmula:C22H32O4Forma y color:SolidPeso molecular:360.49ORM-10103
CAS:<p>ORM-10103 is a novel potent and selective inhibitor of the Na+/Ca2+ exchanger (NCX).ORM-10103 inhibited NCX currents with estimated IC50 values of 55 and 67 nM</p>Fórmula:C20H16N2O4Pureza:99.9%Forma y color:SolidPeso molecular:348.35R-(-)-Niguldipine hydrochloride
CAS:<p>R-(-)-Niguldipine HCl: L-type Ca2+ blocker, K+ agonist, α1A antagonist; lowers blood pressure; weaker enantiomer.</p>Fórmula:C36H40ClN3O6Forma y color:SolidPeso molecular:646.17Ionomycin calcium
CAS:<p>Ionomycin calcium (SQ23377 calcium) is an effective and selective calcium ionophore, exhibiting high specificity for calcium ions. Cost-effective and quality-assured.</p>Fórmula:C41H70CaO9Pureza:98% - 98.11%Forma y color:SolidPeso molecular:747.07(R)-Lercanidipine Hydrochloride
CAS:Producto controladoFórmula:C36H41N3O6·ClHForma y color:NeatPeso molecular:648.19(S)-Lercanidipine Hydrochloride
CAS:Producto controladoFórmula:C36H41N3O6·ClHForma y color:NeatPeso molecular:648.19Falipamil
CAS:Producto controlado<p>Applications Falipamil is a specific bradycardic agent and a calcium channel blocker.<br>References Boucher, M., et al.: Eur. J. Pharmacol., 306, 93 (1996), Mubagwa, K., et al.: Arch. Int. Pharmacodyn. Ther., 286, 71 (1987), Chaudhry, A., et al.: Development Cardiovascular Medicine, 46, 196 (1985), Ogiwara, Y., et al.: Jpn Heart J., 29, (1988)<br></p>Fórmula:C24H32N2O5Forma y color:NeatPeso molecular:428.523-Desethyl-3-(2-phthalimidoethyl) Phthaloyl Amlodipine
Producto controlado<p>Stability Light and Temperature Sensitive<br>Applications 3-Desethyl-3-(2-phthalimidoethyl) Phthaloyl Amlodipine is a derivative of Amlodipine (A633495); a dihydropyridine calcium channel blocker where activity mainly resides in the (-)-isomer.<br>References Arrowsmith, J.E., et al.: J. Med. Chem., 29, 1696 (1986); Burges, R.A., et al.: J. Cardiovasc. Pharmacol., 9, 110 (1987); Haria, M., et al.: Drugs, 50, 560 (1995)<br></p>Fórmula:C36H30ClN3O9Forma y color:NeatPeso molecular:684.091Dihydrocinnamyl Cilnidipine
Producto controlado<p>Applications Dihydrocinnamyl Cilnidipine is a metabolite of Cilnidipine (C441375); a dihydropyridine calcium channel blocker.<br>References Ikeda, K., et al.: Oyo Yakuri, 44, 433 (1992); Hosono, M., et al.: J. Pharmacobio-Dyn., 15, 547, (1992); Ishii, M.: Japan Pharmacol. Ther., 21, 59 (1993)<br></p>Fórmula:C27H30N2O7Forma y color:NeatPeso molecular:494.54Halofuginone
CAS:<p>Halofuginone (RU-19110) inhibits prolyl-tRNA synthetase (Ki=18.3 nM), down-regulates Smad3, and blocks TGF-β at 10 ng/ml.</p>Fórmula:C16H17BrClN3O3Pureza:99.53%Forma y color:Off-White SolidPeso molecular:414.68Verapamil
CAS:<p>Verapamil (CP-16533-1), an oral calcium channel blocker, inhibits P-gp and CYP3A4, used for hypertension, arrhythmias, and angina research.</p>Fórmula:C27H38N2O4Pureza:99.61% - 99.93%Forma y color:OilPeso molecular:454.6Ronipamil
CAS:<p>Ronipamil is an analogue of verapamil that used as a calcium entry blocker.</p>Fórmula:C32H48N2Forma y color:SolidPeso molecular:460.74Lercanidipine, (S)-
CAS:<p>(S)-Lercanidipine: a dihydropyridine calcium blocker with prolonged antihypertensive and kidney-protective properties.</p>Fórmula:C36H41N3O6Pureza:98%Forma y color:SolidPeso molecular:611.73Riodipine
CAS:<p>Riodipine, a calcium channel blocker, is used as cardiovascular drugs.</p>Fórmula:C18H19F2NO5Pureza:98%Forma y color:SolidPeso molecular:367.34Hexadecylphosphoserine
CAS:<p>Hexadecylphosphoserine is a representative growth inhibitor.</p>Fórmula:C19H40NO6PPureza:98%Forma y color:SolidPeso molecular:409.5β-Amino Acid Imagabalin Hydrochloride
CAS:<p>β-Amino Acid Imagabalin Hydrochloride is the voltage-dependent calcium channel ligand for the α2δ subunit.</p>Fórmula:C9H20ClNO2Pureza:98%Forma y color:SolidPeso molecular:209.71JTV-519 fumarate
CAS:<p>Ryanodine receptor (RyR) inhibitor; stabilizes RyR2 in a closed conformation. Exhibits antiarrhythmic and cardioprotective properties in vivo.</p>Fórmula:C29H36N2O6SForma y color:SolidPeso molecular:540.67Dopropidil hydrochloride
CAS:<p>Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris.</p>Fórmula:C20H36ClNO2Forma y color:SolidPeso molecular:357.96Carboxyamidotriazole
CAS:<p>Carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways.</p>Fórmula:C17H12Cl3N5O2Pureza:98%Forma y color:SolidPeso molecular:424.67SCH00013
CAS:<p>SCH00013 is a cardiotonic that enhances myofibrillar Ca++ sensitivity, with notable effects at pH 7.2-7.4.</p>Fórmula:C18H20N4O2Pureza:98%Forma y color:SolidPeso molecular:324.38GZ4
CAS:<p>GZ4 is a Ca2+ currents inhibitor, acting on cell surface channels.</p>Fórmula:C11H17NO2Pureza:98%Forma y color:SolidPeso molecular:195.26BN 50341
CAS:<p>BN 50341 is an inhibitor of antithrombotic platelet activating factor.</p>Fórmula:C32H41ClN2O4Pureza:98%Forma y color:SolidPeso molecular:553.13RQ-00311651
CAS:<p>RQ-00311651 is a novel T-type Ca2+ channel blocker. RQ-00311651 also inhibited high K-induced Ca signaling in those cells.</p>Fórmula:C19H18F3N5O2Forma y color:SolidPeso molecular:405.37EO-122
CAS:<p>EO-122, a calcium channel antagonist and sodium channel antagonist, is used potentially for the treatment of arrhythmia.</p>Fórmula:C16H23ClN2OForma y color:SolidPeso molecular:294.82Gallopamil 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%Forma y color:SolidPeso molecular:521.09AMG-1
CAS:<p>AMG-1 inhibits CRAC channels, blocks effector T cells, not regulatory ones, and reduces EAE progression.</p>Fórmula:C18H9ClF5N3OForma y color:SolidPeso molecular:413.73RyRs activator 3
CAS:<p>RyRs activator 3 (compound A4) serves as an insecticide highly effective against both the diamondback moths, M.</p>Fórmula:C23H19BrCl2N6O3Pureza:98%Forma y color:SolidPeso molecular:578.25Hns 32
CAS:<p>Hns 32 possesses antiarrhythmic properties in dog and guinea pig hearts. It also has vasodilator action.</p>Fórmula:C24H29N3Pureza:98%Forma y color:SolidPeso molecular:359.51A 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%Forma y color:SolidPeso molecular:307.35Methsuximide
CAS:<p>Methsuximide is an anticonvulsant agent which appeared to be effective in petit mal, psychomotor and focal motor attacks [1].</p>Fórmula:C12H13NO2Forma y color:Crystals From Dilute Alcohol SolidPeso molecular:203.243',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%Forma y color: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:C26H24N4O2Forma y color:SolidPeso molecular:424.49Cyclic ADP-ribose
CAS:<p>cADPR, made from NAD+, boosts calcium in cells via Ryanodine receptors and TRPM2 channels.</p>Fórmula:C15H21N5O13P2Pureza:98%Forma y color:Lyophilized PowderPeso molecular:541.3Aladorian
CAS:<p>Aladorian (ARM036), a benzothiazepine, has anti-arrhythmic properties for heart failure and CPVT research.</p>Fórmula:C12H13NO4SPureza:98%Forma y color:SolidPeso molecular:267.3Aprindine hydrochloride
CAS:<p>Aprindine HCl, a Class 1b antiarrhythmic, treats heart arrhythmias, outperforming digoxin in delaying atrial fibrillation. It's effective orally.</p>Fórmula:C22H31ClN2Forma y color:SolidPeso molecular:358.95Levamlodipine gentisate
CAS:<p>Levamlodipine gentisate, an active amlodipine enantiomer, is a dihydropyridine calcium channel blocker for treating hypertension and angina.</p>Fórmula:C27H31ClN2O9Pureza:98%Forma y color:SolidPeso molecular:563JTV-519
CAS:<p>K201 (JTV-519) is a Ca2+-dependent blocker and prevents abnormal Ca(2+) leak from the sarcoplasmic reticulum in the ischemic heart and skeletal muscle (SkM) by</p>Fórmula:C25H33ClN2O2SPureza:99.88%Forma y color:SolidPeso molecular:461.06BK 129
CAS:<p>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.</p>Fórmula:C22H36N2O4Pureza:98%Forma y color:SolidPeso molecular:392.53S-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%Forma y color:SolidPeso molecular:386.46Flordipine
CAS:<p>Flordipine is used as a calcium channel blocker.</p>Fórmula:C26H33F3N2O5Pureza:98%Forma y color:SolidPeso molecular:510.55Niguldipine 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%Forma y color:SolidPeso molecular:609.71CGP 28392
CAS:<p>CGP 28392 is used as a partial calcium channel agonist.</p>Fórmula:C18H17F2NO5Pureza:98%Forma y color:SolidPeso molecular:365.33(Rac)-MEM 1003
CAS:<p>MEM-1003, a calcium channel blocker, is used potentially for the treatment of bipolar disorders.</p>Fórmula:C22H25ClN2O5Forma y color:SolidPeso molecular:432.9Topiramate lithium
CAS:<p>Topiramate lithium: antiepileptic, GluR5 antagonist, enhances GABA, inhibits kainate/AMPA, Na+/Ca2+ channels; ↑ K+ conductance; ↓ carbonic anhydrase.</p>Fórmula:C12H20LiNO8SForma y color:SolidPeso molecular:345.29TTA-Q6(isomer)
CAS:<p>TTA-Q6(isomer) is an isomer of TTA-Q6. TTA-Q6 is a selective antagonist of the T-type Ca2+ channel.</p>Fórmula:C20H15ClF3N3OPureza:98%Forma y color:SolidPeso molecular:405.8PD0176078
CAS:<p>PD0176078 () is a newly blocker of N-type Calcium channel.</p>Fórmula:C23H30F2N2OPureza:99.72%Forma y color:SolidPeso molecular:388.49Diproteverine
CAS:<p>Diproteverine is a calcium antagonist, it has antianginal property.</p>Fórmula:C26H35NO4Pureza:98%Forma y color:SolidPeso molecular:425.56McN5691
CAS:<p>McN5691 is a voltage sensitive calcium channel blocker.</p>Fórmula:C30H35NO3Pureza:98.93% - 99.38%Forma y color:SolidPeso molecular:457.6ML218
CAS:<p>ML218 is an inhibitor of T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3).ML218 inhibits the synaptic activity of subthalamic nucleus (STN) neurons.</p>Fórmula:C19H26Cl2N2OPureza:99.2% - 99.45%Forma y color:SolidPeso molecular:369.33Dopropidil
CAS:<p>Dopropidil: anti-angina calcium regulator with anti-ischemic properties in animal models.</p>Fórmula:C20H35NO2Pureza:98%Forma y color:SolidPeso molecular:321.5PD-151307
CAS:<p>PD-151307 is used as an N-type calcium channel blocker.</p>Fórmula:C33H47N3O5Pureza:98%Forma y color:SolidPeso molecular:565.74AJG-049 HCl
CAS:<p>AJG-049 HCl is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).</p>Fórmula:C27H31ClN2O2Forma y color:SolidPeso molecular:451.01Cavα2δ1&NET-IN-2
CAS:<p>Cavα2δ1&NET-IN-2 .</p>Fórmula:C22H26N6O2SForma y color:SolidPeso molecular:438.55Halofuginone hydrobromide
CAS:<p>Halofuginone specifically inhibits collagen type I and MMP-2 gene expression, which may result in the suppression of angiogenesis and tumor cell growth.</p>Fórmula:C16H17BrClN3O3·HBrPureza:97.01% - 99.73%Forma y color:SolidPeso molecular:495.59TTA-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%Forma y color:SolidPeso molecular:405.8GSK-5503A
CAS:<p>GSK-5503A is a novel channel blocker of CRAC.</p>Fórmula:C23H17F2N3O2Pureza:98%Forma y color:SolidPeso molecular:405.4Gallopamil hydrochloride
CAS:<p>Gallopamil hydrochloride (Methoxyverapamil hydrochloride) is an antagonist of phenylalkylamine calcium.</p>Fórmula:C28H41ClN2O5Pureza:99.86%Forma y color:SolidPeso molecular:521.09TDN345
CAS:<p>TDN345 is a antagonist of Ca2+, for the treatment of vascular and senile dementia including Alzheimer's disease.</p>Fórmula:C28H34F2N2O2Pureza:98%Forma y color:SolidPeso molecular:468.58Teludipine hydrochloride
CAS:<p>Teludipine hydrochloride is a blocker of lipophilic calcium channel.</p>Fórmula:C28H39ClN2O6Pureza:98%Forma y color:SolidPeso molecular:535.07Nemadipine-A
CAS:<p>Nemadipine A blocks L-type Ca2+ channels, alters C. elegans morphology, boosts TRAIL's cancer kill rate, and lowers Survivin in A549 cells.</p>Fórmula:C19H18F5NO4Forma y color:SolidPeso molecular:419.3418:0 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%Forma y color:SolidPeso molecular:481.6AE0047 Hydrochloride
CAS:<p>AE0047 Hydrochloride is a blocker of calcium, and used in the research of the hypertensive disease.</p>Fórmula:C41H43ClN4O6Pureza:98%Forma y color:SolidPeso molecular:723.26Ned-K
CAS:<p>Ned-K blocks NAADP, reduces heart ischemia-reperfusion calcium waves.</p>Fórmula:C31H31N5O3Forma y color:SolidPeso molecular:521.61piCRAC-1
CAS:<p>piCRAC-1 is a powerful inhibitor of the photoinducible Ca2+ release-activated Ca2+ (CRAC) channel.</p>Fórmula:C17H10F6N4Forma y color:SolidPeso molecular:384.28Semotiadil recemate fumarate
CAS:<p>Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel antagonist of vasoselective Ca2+ channel.</p>Fórmula:C33H36N2O10SPureza:98%Forma y color:SolidPeso molecular:652.71Norverapamil
CAS:<p>Norverapamil is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function .</p>Fórmula:C26H36N2O4Pureza:98%Forma y color:SolidPeso molecular:440.58Levosemotiadil
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%Forma y color:SolidPeso molecular:536.64TTA-A8
CAS:<p>TTA-A8 is an antagonist of T-type calcium channel.</p>Fórmula:C22H21F3N4O2Pureza:99.22%Forma y color:SolidPeso molecular:430.42YM 244769 hydrochloride
CAS:<p>inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)</p>Fórmula:C26H23ClFN3O3Pureza:98%Forma y color:SolidPeso molecular:479.93YS-201
CAS:<p>YS-201 is an antagonist of dihydropyridine-type calcium channel.</p>Fórmula:C24H31N3O6Pureza:98%Forma y color:SolidPeso molecular:457.52BMS-192364
CAS:<p>BMS-192364 is a bio-active chemical.</p>Fórmula:C15H9ClF3N3O2Forma y color:SolidPeso molecular:355.70trans-Ned 19
CAS:<p>trans-Ned 19 blocks NAADP and TPC, hindering calcium signaling and aorta relaxation at low histamine levels.</p>Fórmula:C30H31FN4O3Pureza:98%Forma y color:SolidPeso molecular:514.59Dehydronitrosonisoldipine
CAS:<p>Dehydronitrosonisoldipine blocks SARM1, slows axon decay & cADPR synthesis; useful in neurodegeneration research.</p>Fórmula:C20H22N2O5Pureza:99.68%Forma y color:SolidPeso molecular:370.4DHP-218
CAS:<p>DHP-218, a calcium channel blocker, inhibits rat aorta contractions; pA2: 9.11, IC50: 6.3 nmol/L (high K+) & 66 nmol/L (phenylephrine).</p>Fórmula:C18H21N2O7PPureza:98%Forma y color:SolidPeso molecular:408.34Lidoflazine
CAS:<p>Lidoflazine: antianginal, blocks HERG K+ & Ca channels, risks QT prolongation & arrhythmia.</p>Fórmula:C30H35F2N3OPureza:98%Forma y color:SolidPeso molecular:491.62AH-1058 HCl
CAS:<p>AH-1058 HCl is a lipophilic antiarrhythmic calcium channel blocker.</p>Fórmula:C30H29ClN2O3Pureza:98%Forma y color:SolidPeso molecular:501.02TMB 8 (hydrochloride)
CAS:<p>TMB 8 blocks nAChRs (IC50: 390-480 nM), reduces Ca2+ in muscles, hinders rabbit aorta contraction at 50 μM, and inhibits PKC dose-dependently.</p>Fórmula:C22H38ClNO5Forma y color:White SolidPeso molecular:431.99SB-237376 HCl
CAS:<p>SB-237376 HCl (SB-237376 hydrochloride) is a calcium and potassium channel antagonist used in the treatment of cardiac arrhythmias.</p>Fórmula:C20H26ClN3O5Pureza:98.70%Forma y color:SolidPeso molecular:423.89NC 1100
CAS:<p>NC 1100 is a calcium channel antagonist.</p>Fórmula:C27H34Cl2N2O3Pureza:98%Forma y color:SolidPeso molecular:505.48RS 30026
CAS:<p>RS 30026 is a potent calcium channel agonist.</p>Fórmula:C23H21NO4SForma y color:SolidPeso molecular:407.48(R)-Lercanidipine hydrochloride
CAS:<p>(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.</p>Fórmula:C36H42ClN3O6Pureza:98%Forma y color:SolidPeso molecular:648.2CaV1.3 antagonist-1
CAS:<p>CaV1.3 antagonist-1 is a selective CaV1.3L-type calcium channel antagonist useful for researching neurological disorders and cardiovascular diseases.</p>Fórmula:C17H19ClN2O3Forma y color:SolidPeso molecular:334.8Hyperforin dicyclohexylammonium salt
CAS:<p>Hyperforin dicyclohexylammonium is a TRPC6 activator and antidepressant that modulates Ca2+ levels.</p>Fórmula:C47H75NO4Pureza:98%Forma y color:SolidPeso molecular:718.1Palonidipine
CAS:<p>Palonidipine is an antagonist of calcium, is potential for the therapy of angina-pectoris and hypertension.</p>Fórmula:C29H34FN3O6Pureza:98%Forma y color:SolidPeso molecular:539.6ITH-12575
CAS:<p>ITH-12575 is an inhibitor of Mitochondrial Na+/Ca2+ exchange (mNCX). ITH12575 reduces Ca(2+) influx through CALHM1 at low micromolar concentrations.</p>Fórmula:C18H18ClNOSForma y color:SolidPeso molecular:331.86ML218 hydrochloride
CAS:<p>ML218 hydrochloride inhibits T-type Ca2+ channels Cav3.1-3.3; most effective on Cav3.2 and Cav3.3 (IC50s: 310 nM, 270 nM).</p>Fórmula:C19H27Cl3N2OPureza:98%Forma y color:SolidPeso molecular:405.79UK51656
CAS:<p>UK51656 is an antagonist of calcium (IC50: 4 nM).</p>Fórmula:C22H28ClN3O6Pureza:98%Forma y color:SolidPeso molecular:465.93JTV-519 free base
CAS:<p>JTV-519 free base (K201 free base), recognized for its antiarrhythmic and cardioprotective properties, functions as a Ca2+-dependent blocker of sarcoplasmic</p>Fórmula:C25H32N2O2SPureza:98%Forma y color:SolidPeso molecular:424.6A 39355
CAS:<p>A 39355 may specifically overcome multidrug resistance without the serious hypotensive effects associated with calcium antagonists.</p>Fórmula:C28H39Cl2N3OPureza:98%Forma y color:SolidPeso molecular:504.54Sadopine
CAS:<p>Sadopine is a high-affinity radioligand for DHP receptor in L-type Ca2+ channels, suitable for tissue and membrane labeling.</p>Fórmula:C30H40F3N3O7SForma y color:SolidPeso molecular:643.71(S)-Lercanidipine hydrochloride
CAS:<p>(S)-Lercanidipine hydrochloride is the S-enantiomer of Lercanidipine hydrochloride. (S)-lercanidipine hydrochloride is a potent blocker of calcium channel.</p>Fórmula:C36H42ClN3O6Pureza:98%Forma y color:SolidPeso molecular:648.19SQ-31765
CAS:<p>SQ-31765 is a blocker of benzazepine calcium channel.</p>Fórmula:C24H27F3N2O4Pureza:98%Forma y color:SolidPeso molecular:464.48Anipamil
CAS:<p>Anipamil is a long-acting blocker of calcium channel,and for the treatment of cardiovascular disease.</p>Fórmula:C34H52N2O2Pureza:98%Forma y color:SolidPeso molecular:520.79SOCE 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%Forma y color:SolidPeso molecular:513.47Norbormide
CAS:<p>Norbormide is a toxic compound used as a rodenticide. It has several mechanisms of action, acting as a vasoconstrictor and calcium channel blocker.</p>Fórmula:C33H25N3O3Pureza:98%Forma y color:Crystals From Methylene Chloride + Ether Norbormide Is A Colorless To Off-White Crystalline Powder Used As A Selective Rat Poison (Epa 1998)Peso molecular:511.57Lercanidipine. (R)-
CAS:<p>(R)-Lercanidipine enantiomer: antihypertensive, blocks L-type Ca2+ channels, dilates blood vessels.</p>Fórmula:C36H41N3O6Forma y color:SolidPeso molecular:611.73TTA-P2
CAS:<p>TTA-P2: potent CNS-penetrating T-type Ca2+ channel blocker; eliminates Cav3.1 window currents.</p>Fórmula:C21H29Cl2FN2O2Forma y color:SolidPeso molecular:431.37NPS-2143
CAS:<p>NPS-2143 (SB 262470A) is a novel potent and selective antagonist of Ca(2+) receptor.</p>Fórmula:C24H25ClN2O2Pureza:99.56%Forma y color:SolidPeso molecular:408.92Leconotide
CAS:<p>Leconotide is a calcium channel blocker and antihyperalgesia agent; isolated from the venom of the cone snail, Conus catus.</p>Fórmula:C107H179N35O36S7Forma y color:SolidPeso molecular:2756.23YS-035 hydrochloride
CAS:<p>inhibitor of outward K+ currents</p>Fórmula:C21H30ClNO4Pureza:98%Forma y color:SolidPeso molecular:395.92N-Salicyloyltryptamine
CAS:<p>N-Salicyloyltryptamine (STP): a tryptamine with anticonvulsant, anti-inflammatory, analgesic effects; inhibits Na+, Ca2+, K+ channels (IC50 34.6 μM).</p>Fórmula:C17H16N2O2Forma y color:SolidPeso molecular:280.32PD 122860
CAS:<p>PD 122860 is a dihydropyridine enhancing heart contractility, altering ECG, and relaxing aortic rings.</p>Fórmula:C23H20F3N3O4SPureza:98%Forma y color:SolidPeso molecular:491.48Kadethrin
CAS:<p>Kadethrin is a synthetic pyrethroid. It was used as a pesticide.</p>Fórmula:C23H24O4SPureza:98%Forma y color:Yellow-Brown Viscous Oil SolidPeso molecular:396.5UK-52831
CAS:<p>UK-52831, a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.</p>Fórmula:C22H26Cl2N6O5Pureza:98%Forma y color:SolidPeso molecular:525.39GSK-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:C18H11F6N3OForma y color:SolidPeso molecular:399.29JTV-519 hemifumarate
CAS:<p>JTV-519 hemifumarate: Ca2+ blocker, SERCA inhibitor, ryanodine receptor partial agonist; antiarrhythmic, cardioprotective.</p>Fórmula:C54H68N4O8S2Pureza:98%Forma y color:SolidPeso molecular:965.28Diltiazem malate
CAS:<p>Diltiazem malate is an ACE inhibitor and non-dihydropyridine calcium channel blocker used in the treatment of hypertension.</p>Fórmula:C26H32N2O9SForma y color:SolidPeso molecular:548.60Ethacrynate Sodium
CAS:<p>Ethacrynate Sodium, a sodium salt, blocks chloride, potassium, and sodium transport mainly in Henle's loop.</p>Fórmula:C13H12Cl2NaO4Pureza:98%Forma y color:SolidPeso molecular:326.12IDO1-IN-19
CAS:<p>IDO1-IN-19 (Compound 17) is a potent inhibitor of IDO1 and has potential for cancer disease research.</p>Fórmula:C25H22F4N2O3Forma y color:SolidPeso molecular:474.45(R)-Amlodipine
CAS:<p>(R)-Amlodipine is the R-enantiomer of Amlodipine and functions as an orally active dihydropyridine calcium channel blocker with antianginal properties.</p>Fórmula:C20H25ClN2O5Pureza:99.977%Forma y color:SolidPeso molecular:408.88Lemildipine
CAS:<p>Lemildipine is a new blocker of dihydropyridine calcium entry.</p>Fórmula:C20H22Cl2N2O6Forma y color:SolidPeso molecular:457.3CXL-1020
CAS:<p>CXL-1020, a HNO prodrug, enhances heart muscle function & relaxation, aiding in heart failure research.</p>Fórmula:C7H9NO5S2Forma y color:SolidPeso molecular:251.28SM-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%Forma y color:SolidPeso molecular:489.52(2R/S)-6-PNG
CAS:<p>(2R/S)-6-PNG (6-Prenylnaringenin) from hops is a natural histone deacetylase inhibitor that blocks T-type calcium channels reducing neurogenicity in mice.</p>Fórmula:C20H20O5Pureza:98%Forma y color:SolidPeso molecular:340.37NP-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%Forma y color:SolidPeso molecular:469.57ORM-10962
CAS:<p>ORM-10962 is a potent, highly selective inhibitor of sodium-calcium exchanger (NCX) (for the reverse and forward mode inhibition with IC50 values of 67 and 55</p>Fórmula:C27H29N3O4Pureza:98%Forma y color:SolidPeso molecular:459.54Cavα2δ1&NET-IN-1
CAS:<p>Cavα2δ1&NET-IN-1 .</p>Fórmula:C23H26N4O2SForma y color:SolidPeso molecular:422.54KB-130015
CAS:<p>KB-130015, a activator of hERG1 potassium channels, blocks native and recombinant hERG1 channels at high voltages.</p>Fórmula:C18H14I2O4Pureza:98%Forma y color:SolidPeso molecular:548.11Watanidipine dihydrochloride
CAS:<p>Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.</p>Fórmula:C41H44Cl2N4O6Pureza:98%Forma y color:SolidPeso molecular:759.73
![4-(2-Chlorophenyl)-2-methyl-5-oxo-4,4a,5,7,8,10-hexahydro-1H-pyrido[2',3':2,3]azeto[2,1-c][1,4]oxa…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FC609788.webp&w=3840&q=75)
