Canais de Cálcio
Os canais de cálcio são proteínas de membrana que regulam o fluxo de íons de cálcio para dentro e fora das células, o que é essencial para várias funções celulares, incluindo a contração muscular, a liberação de neurotransmissores e a expressão gênica. A desregulação da atividade dos canais de cálcio está associada a condições como hipertensão, arritmias cardíacas e distúrbios neurológicos. Na CymitQuimica, oferecemos uma ampla seleção de moduladores de canais de cálcio para apoiar sua pesquisa em saúde cardiovascular, neurobiologia e transdução de sinais.
Foram encontrados 541 produtos de "Canais de Cálcio"
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Efonidipine
CAS:Efonidipine (NZ-105)(NZ-105) is a dihydropyridine calcium channel blocker, blocking both T-type and L-type calcium channels.Fórmula:C34H38N3O7PPureza:98.35% - 99.47%Cor e Forma:SolidPeso molecular:631.66Dronedarone
CAS:Dronedarone (SR 33589) is an amiodarone analogue which has an effective and promising treatment for Atrial fibrillation.Fórmula:C31H44N2O5SPureza:98.85% - 99.99%Cor e Forma:SolidPeso molecular:556.76Etripamil
CAS:Etripamil is a fast-acting intranasal L-type calcium-channel blocker for Paroxysmal Supraventricular Tachycardia.Fórmula:C27H36N2O4Pureza:99.47% - 99.83%Cor e Forma:SolidPeso molecular:452.59Ref: TM-T15257
1mg55,00€2mg79,00€5mg116,00€10mg172,00€25mg311,00€50mg472,00€100mg707,00€200mg1.111,00€Cyclopiazonic acid
CAS:Cyclopiazonic acid (CPA) is a neurotoxic secondary metabolite (SM) made by A.Fórmula:C20H20N2O3Pureza:99.27% - 99.80%Cor e Forma:SolidPeso molecular:336.38Ned 19
CAS:Ned 19 inhibits tumor growth, vascularization, lung metastases in mice, and is a selective NAADP antagonist.Fórmula:C30H31FN4O3Pureza:99.66%Cor e Forma:SolidPeso molecular:514.59Ref: TM-T12205
1mg64,00€2mg92,00€5mg137,00€10mg202,00€25mg341,00€50mg507,00€100mg722,00€500mg1.454,00€1mL*10mM (DMSO)155,00€Levamlodipine besylate
CAS:Levamlodipine besylate, or S-amlodipine (CAS 103129-82-4), is the active enantiomer of amlodipine, used to treat hypertension and angina.Fórmula:C26H31ClN2O8SPureza:99.78% - 99.79%Cor e Forma:SolidPeso molecular:567.05OPHIOPOGONIN D
CAS:Ophiopogonin D is a natural product,and is a CYP2J3 inducer that significantly inhibits Ang II induced NF-κB nuclear translocation.Fórmula:C44H70O16Pureza:99.46% - ≥95%Cor e Forma:SolidPeso molecular:855.02Yangambin
CAS:Yangambin: selective PAF antagonist, hypotensive, inhibits Ca2+ influx, induces peripheral vasodilation, affects CNS.Fórmula:C24H30O8Pureza:98.02%Cor e Forma:SolidPeso molecular:446.49Taurolithocholic acid sodium salt
CAS:Taurolithocholic acid sodium salt (Sodium taurolithocholate) is the major human metabolite, a bile acid which inhibits radioligand binding to muscarinic M1, butFórmula:C26H44NNaO5SPureza:99.79% - 99.93%Cor e Forma:SolidPeso molecular:505.69JNJ-26990990
CAS:"JNJ-26990990: broad-spectrum anticonvulsant, less side effects than topiramate, potential for pain and depression treatment; Phase II in 2007."Fórmula:C9H10N2O2S2Pureza:97.37%Cor e Forma:SolidPeso molecular:242.32Ref: TM-T27673
1mg131,00€5mg286,00€10mg424,00€25mg702,00€50mg938,00€100mg1.311,00€1mL*10mM (DMSO)261,00€Bay 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%Cor e Forma:Yellow PowderPeso molecular:356.3SEA0400
CAS:SEA0400 is a selective inhibitor of the Na+/Ca2+ exchanger.Fórmula:C21H19F2NO3Pureza:98.88% - 99.55%Cor e Forma:SolidPeso molecular:371.38Ref: TM-T3508
1mg39,00€2mg50,00€5mg81,00€10mg131,00€25mg230,00€50mg378,00€100mg567,00€500mg1.254,00€1mL*10mM (DMSO)74,00€Pyridaben
CAS:Pyridaben is a METI acaricide that inhibits mitochondrial electron transport at complex I (METI; Ki = 0.36 nmol/mg protein in rat brain mitochondria).Fórmula:C19H25ClN2OSPureza:97.11% - 99.75%Cor e Forma:SolidPeso molecular:364.93Homo-VK-II-36
CAS:Homo-VK-II-36 (Homo-V-II-36) is a carvedilol analogue that acts by inhibiting store- overload-induced calcium release through the RyR2 channel.Fórmula:C27H28N2O5Pureza:99.26%Cor e Forma:SolidPeso molecular:460.52Methyl homoveratrate
CAS:Methyl homoveratrate, a McN5691 (RWJ-26240) metabolite detected in vivo in plasma, urine, and fecal extracts, functions as a voltage-sensitive calcium channelFórmula:C11H14O4Pureza:99.48%Cor e Forma:SolidPeso molecular:210.23Lomerizine
CAS:<p>Lomerizine, a blocker of diphenylmethylpiperazine Ca2+ channel, is used to prevent migraines.</p>Fórmula:C27H30F2N2O3Cor e Forma:SolidPeso molecular:468.54Amlodipine mesylate
CAS:Amlodipine mesylate, an oral dihydropyridine Ca2+ blocker, treats angina, hypertension, and may be used in cancer research.Fórmula:C21H29ClN2O8SCor e Forma:SolidPeso molecular:504.98Thapsigargin
CAS:Thapsigargin is a natural product, an inhibitor of sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA) and an endoplasmic reticulum stress inducer.Fórmula:C34H50O12Pureza:99.07% - 99.3%Cor e Forma:Colourless FilmPeso molecular:650.75HC-056456
CAS:HC-056456 (3,4-Bis(2-thienoyl)-1,2,5-oxadiazole-N-oxide) is a CatSper channel modulator.Fórmula:C12H6N2O4S2Pureza:99.62% - 99.65%Cor e Forma:SolidPeso molecular:306.32Ref: TM-T4604
1mg35,00€2mg48,00€5mg70,00€10mg96,00€25mg170,00€50mg274,00€100mg454,00€1mL*10mM (DMSO)77,00€TGR5 Receptor Agonist
CAS:TGR5 is a potent TGR5(GPCR19) agonist.Fórmula:C18H14Cl2N2O2Pureza:99.77% - ≥95%Cor e Forma:SolidPeso molecular:361.22Bifemelane
CAS:Bifemelane, a nootropic, releases Ca2+ from stores and enables its entry via channels for astrocyte research.Fórmula:C18H23NOCor e Forma:SolidPeso molecular:269.38Levamlodipine hydrochloride
CAS:Levamlodipine hydrochloride is a medication used to lower blood pressure and prevent chest pain.Fórmula:C20H26Cl2N2O5Cor e Forma:SolidPeso molecular:445.34Efonidipine hydrochloride
CAS:Efonidipine HCl (NZ-105) blocks T-type/L-type calcium channels; used in hypertension treatment.Fórmula:C34H39ClN3O7PCor e Forma:SolidPeso molecular:668.12ABT-639 hydrochloride
CAS:ABT-639 hydrochloride is a selective, novel T-type Ca2+ channel blocker.Fórmula:C20H21Cl2F2N3O3SCor e Forma:SolidPeso molecular:492.36Bepridil free base
CAS:Bepridil: Class IV anti-arrhythmic, calcium blocker, dilates coronary arteries.Fórmula:C24H34N2OCor e Forma:SolidPeso molecular:366.54Azumolene sodium anhydrous
CAS:Azumolene sodium, a muscle relaxant, blocks calcium release from muscles and halts SOCE linked to RyR1 except when induced by thapsigargin.Fórmula:C13H8BrN4NaO3Cor e Forma:SolidPeso molecular:371.13Ginsenoside Rd
CAS:<p>Ginsenoside Rd (Gypenoside VIII) may have properties that inhibit or prevent the growth of tumors.</p>Fórmula:C48H82O18Pureza:99.13% - 99.92%Cor e Forma:SolidPeso molecular:947.15Mirogabalin besylate
CAS:Mirogabalin besylate is an oral α2δ ligand for voltage-gated calcium channels, with Kd values of 13.5-47.6 nM across species.Fórmula:C18H25NO5SCor e Forma:SolidPeso molecular:367.46ABT-639
CAS:ABT-639 is a potent and selective T-type calcium channel blocker.Fórmula:C20H20ClF2N3O3SPureza:99.12% - 99.77%Cor e Forma:SolidPeso molecular:455.91Ref: TM-T3703
2mg35,00€5mg52,00€10mg80,00€25mg169,00€50mg283,00€100mg469,00€200mg682,00€1mL*10mM (DMSO)64,00€Mibefradil dihydrochloride
CAS:Mibefradil dihydrochloride (Ro 40-5967 (dihydrochloride)) is an blocker of calcium channel with moderate selectivity for T-type Ca2+ channels (T-type and L-typeFórmula:C29H40Cl2FN3O3Pureza:99.45% - 99.91%Cor e Forma:SolidPeso molecular:568.55L-Phenylalanine-15N
CAS:L-Phenylalanine-15N, essential amino acid, Ca+ channel and NMDARs antagonist, used in food flavors and pharmaceuticals.Fórmula:C9H11NO2Pureza:98.98%Cor e Forma:SolidPeso molecular:166.18VK-II-36
CAS:VK-II-36, a carvedilol analog, suppresses sarcoplasmic reticulum (SR) Ca(2+) release but does not block the β-receptor.Fórmula:C26H26N2O5Pureza:99.12%Cor e Forma:SolidPeso molecular:446.49Ranolazine
CAS:Ranolazine (RS 43285-003) inhibits calcium uptake, treats chronic angina by targeting sodium/calcium channels to modulate intracellular sodium.Fórmula:C24H33N3O4Pureza:98.13%Cor e Forma:White SolidPeso molecular:427.54Mirogabalin
CAS:<p>Mirogabalin (DS5565) is a calcium channel blocker with analgesic effects.</p>Fórmula:C12H19NO2Pureza:98.57%Cor e Forma:SolidPeso molecular:209.28NP118809
CAS:<p>NP118809 (39-1B4) is a potent N-type calcium channel blocker(IC50 : 0.11 μM).</p>Fórmula:C32H32N2OPureza:97.74% - 98.68%Cor e Forma:SolidPeso molecular:460.61Pyr6
CAS:Pyr6 (N-[4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl]phenyl]-3-fluoro-4-pyridinecarboxamide) is a selective TRPC3 inhibitor with IC50 of 0.49 uM(Ca2+ influxFórmula:C17H9F7N4OPureza:98.89%Cor e Forma:SolidPeso molecular:418.27Quadrol
CAS:Quadrol (EDTP) is an immunostimulant, accelerated wound healing.Fórmula:C14H32N2O4Pureza:99.91% - 99.92%Cor e Forma:Viscous Liquid Liquid ViscousPeso molecular:292.41S107
CAS:S107 stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.Fórmula:C11H15NOSPureza:99.90%Cor e Forma:SolidPeso molecular:209.31Ref: TM-T3438
2mg38,00€5mg64,00€10mg96,00€25mg158,00€50mg255,00€100mg363,00€200mg515,00€1mL*10mM (DMSO)70,00€Argireline
CAS:Argireline (Acetyl hexapeptide-3) is a peptide that inhibits neurotransmitter release, reducing wrinkles.Fórmula:C34H60N14O12SPureza:96.79% - 99.65%Cor e Forma:White PowderPeso molecular:888.99Praeruptorin E
CAS: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.Fórmula:C24H28O7Pureza:98.04% - 99.95%Cor e Forma: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%Cor e Forma:SolidPeso molecular:564.74Levamlodipine hydrobromide
CAS:Levamlodipine hydrobromide is a medication used to lower blood pressure and prevent chest pain.Fórmula:C20H26BrClN2O5Cor e Forma:SolidPeso molecular:489.79HA-1004 HCl
CAS:HA-1004 is an inhibitor of PKA, cGKI, PKC, MYLK, and calcium channel protein.Fórmula:C12H17Cl2N5O2SCor e Forma:SolidPeso molecular:366.27L-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%Cor e Forma:Solid CrystallinePeso molecular:165.19Azumolene
CAS:Azumolene (EU4093 free base)Fórmula:C13H9BrN4O3Pureza:98.1% - 98.35%Cor e Forma:SolidPeso molecular:349.14Ref: TM-T8815
2mg49,00€5mg73,00€10mg116,00€25mg235,00€50mg373,00€100mg562,00€500mg1.216,00€1mL*10mM (DMSO)82,00€NFAT Inhibitor-2
CAS:NFAT Inhibitor-2 is a compound used as a molecular building block.Fórmula:C22H20F2N2O4SPureza:97.37%Cor e Forma:SolidPeso molecular:446.47Dantrolene sodium hemiheptahydrate
CAS:Dantrolene depresses excitation-contraction coupling in skeletal muscle by binding to the ryanodine receptor 1 and decreasing intracellular calciumFórmula:C14H9N4NaO5·5H2OPureza:99.72%Cor e Forma:Orange PowderPeso molecular:399.29HALOFUGINONE LACTATE
CAS:HALOFUGINONE LACTATE is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D.Fórmula:C19H23BrClN3O6Pureza:99.70% - 99.96%Cor e Forma:SolidPeso molecular:504.8Ref: TM-T8785
2mg42,00€5mg59,00€10mg94,00€25mg130,00€50mg207,00€100mg309,00€200mg462,00€1mL*10mM (DMSO)66,00€Ethacrynic acid
CAS: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。Fórmula:C13H12Cl2O4Pureza:98.61% - 99.85%Cor e Forma:Crystals Physical Description White Solid (Ntp 1992)Peso molecular:303.14Gabapentin hydrochloride
CAS:Gabapentin hydrochloride (Neurontin HCl) is a GABA analogue, used to treat seizures and neuropathic pain.Fórmula:C9H17NO2·HClPureza:99.71%Cor e Forma:Off-White SolidPeso molecular:207.7Cycleanine
CAS:<p>Cycleanine has potent antibacterial, antifungal, antiplasmodial, and cytotoxic activities.</p>Fórmula:C38H42N2O6Pureza:98.04% - 99.57%Cor e Forma:SolidPeso molecular:622.75Pranidipine
CAS:Pranidipine (OPC-13340) is a novel, long-acting 1,4-dihydropyridine calcium channel blocker.Fórmula:C25H24N2O6Pureza:99.95%Cor e Forma: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%Cor e Forma:SolidPeso molecular:355.43Aranidipine
CAS:Aranidipine (MPC1304) (MPC1304) is a calcium channel antagonist with potent and long-lasting antihypertensive effects.Fórmula:C19H20N2O7Pureza:99.15%Cor e Forma:SolidPeso molecular:388.37TTA-A2
CAS:TTA-A2: T-type calcium channel blocker; anticonvulsant targeting Cav3.1, Cav3.2; IC50 of 89/92 nM; potential for treating neurological conditions.Fórmula:C20H21F3N2O2Pureza:99.5% - 99.9%Cor e Forma:SolidPeso molecular:378.39Ref: TM-T8944
1mg104,00€5mg255,00€10mg406,00€25mg745,00€50mg1.064,00€100mg1.406,00€1mL*10mM (DMSO)280,00€Gomisin J
CAS:Gomisin J is a natural product and have vasodilatory activity.Fórmula:C22H28O6Pureza:99.59% - 99.60%Cor e Forma:SolidPeso molecular:388.45Ref: TM-T3904
1mg47,00€2mg65,00€5mg119,00€10mg188,00€25mg329,00€50mg490,00€100mg700,00€1mL*10mM (DMSO)97,00€Fasudil hydrochloride
CAS: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.Fórmula:C14H18ClN3O2SPureza:99.54% - ≥95%Cor e Forma:White SolidPeso molecular:327.83Norfluoxetine Hydrochloride
CAS:Norfluoxetine Hydrochloride (Norfluoxetine HCl) is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.Fórmula:C16H17ClF3NOPureza:99.71%Cor e Forma:SolidPeso molecular:331.76Lanthanum(III) chloride heptahydrate
CAS:Lanthanum(III) chloride blocks divalent cation channels, useful for biochemical research.Fórmula:Cl3H14LaO7Pureza:98%Cor e Forma:White Solid PowderPeso molecular:371.37Ref: TM-T22353
5mg48,00€10mg63,00€25mg93,00€50mg136,00€100mg188,00€200mg283,00€500mg487,00€1mL*10mM (DMSO)50,00€Barnidipine hydrochloride
CAS:Barnidipine HCl is a potent dihydropyridine Ca²⁺ blocker with 0.35 nM IC50 in pig coronary artery.Fórmula:C27H30ClN3O6Pureza:99.88%Cor e Forma:SolidPeso molecular:528Manidipine
CAS:Manidipine (Iperten), a calcium channel blocker, which is dihydropyridine type. It is utilizedFórmula:C35H38N4O6Pureza:99.30%Cor e Forma:SolidPeso molecular:610.7Heteroclitin D
CAS:1. Heteroclitin D can inhibit L-type calcium channels. 2. Heteroclitin D might be a valuable antitumor promoter or chemopreventor.Fórmula:C27H30O8Pureza:99.24% - 99.91%Cor e Forma:SolidPeso molecular:482.52Ref: TM-T3S1916
1mg65,00€5mg170,00€10mg251,00€25mg409,00€50mg563,00€100mg758,00€200mg1.017,00€1mL*10mM (DMSO)192,00€ISX-9
CAS:ISX-9 (Isoxazole 9) is necessary to activate neuron-specific genes as neurogenesis inducer.Fórmula:C11H10N2O2SPureza:97.81% - ≥95%Cor e Forma:SolidPeso molecular:234.27Ref: TM-T2003
2mg48,00€5mg72,00€10mg97,00€25mg155,00€50mg210,00€100mg378,00€500mg889,00€1mL*10mM (DMSO)79,00€YM-58483
CAS:YM-58483 (BTP2) is a specific and effective inhibitor of CRAC channels and subsequent Ca2+ signals.Fórmula:C15H9F6N5OSPureza:99.33% - 99.64%Cor e Forma:SolidPeso molecular:421.32Ref: TM-T3651
1mg35,00€2mg50,00€5mg74,00€10mg115,00€25mg227,00€50mg384,00€100mg560,00€1mL*10mM (DMSO)69,00€Z944
CAS:Z944 is a T-type calcium channel blocker.Fórmula:C19H27ClFN3O2Pureza:99.8% - 99.80%Cor e Forma:SolidPeso molecular:383.89Ref: TM-T29201
1mg52,00€5mg111,00€10mg180,00€25mg359,00€50mg530,00€100mg758,00€200mg1.035,00€1mL*10mM (DMSO)124,00€Barnidipine
CAS:Barnidipine (YM-09730-5(Free base)) is a calcium channel blocker.Fórmula:C27H29N3O6Pureza:99.98%Cor e Forma:SolidPeso molecular:491.54Ref: TM-T7550
1mg46,00€2mg57,00€5mg89,00€10mg123,00€25mg230,00€50mg344,00€100mg520,00€1mL*10mM (DMSO)97,00€Ginsenoside Rf
CAS:Ginsenoside Rf (Panaxoside Rf) is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.Fórmula:C42H72O14Pureza:99.82%Cor e Forma: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%Cor e Forma:SolidPeso molecular:244.2Ginsenoside Ro
CAS:Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist withFórmula:C48H76O19Pureza:98% - 99.66%Cor e Forma:SolidPeso molecular:957.11Isradipine
CAS:Isradipine (PN 200-110), a dihydropyridine, is an antihypertensive calcium channel blocker that dilates arteries and reduces resistance.Fórmula:C19H21N3O5Pureza:99.84% - 99.95%Cor e Forma:Yellow SolidPeso molecular:371.39Ruthenium Red
CAS:Ruthenium Red (Ammoniated ruthenium oxychloride) is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria.Fórmula:Cl6H42N14O2Ru3Pureza:95%Cor e Forma:Purple PowderPeso molecular:786.34Benidipine hydrochloride
CAS:Benidipine hydrochloride (Coniel) , a hydrochloride salt form of benidipine, is used as a blocker of dihydropyridine calcium channel.Fórmula:C28H32ClN3O6Pureza:99.80%Cor e Forma:SolidPeso molecular:542.03Nicardipine
CAS:Nicardipine (Cardene), a calcium channel blockers belonging to the dihydropyridine class, is a drug used to treat angina and high blood pressure.Fórmula:C26H29N3O6Pureza:99.56%Cor e Forma:SolidPeso molecular:479.52Zegocractin
CAS:Zegocractin (CM-4620) is a calcium-release activated calcium-channel (CRAC channel) inhibitor.Fórmula:C19H11ClF3N3O3Pureza:98.82%Cor e Forma:SolidPeso molecular:421.76Ref: TM-TQ0033
1mg126,00€5mg259,00€10mg432,00€25mg715,00€50mg998,00€100mg1.349,00€1mL*10mM (DMSO)283,00€MDK-4025
CAS:<p>MDK-4025 is an inhibitor of the high voltage-activated (HVA) Ca2+ current in pyramidal neurons.</p>Fórmula:C19H15ClOPureza:98.65%Cor e Forma:SolidPeso molecular:294.77Bevantolol hydrochloride
CAS:Bevantolol hydrochloride (NC-1400 hydrochloride) is a β1-adrenoceptor antagonist that treatment angina pectoris and hypertension.Fórmula:C20H28ClNO4Pureza:99.49%Cor e Forma:SolidPeso molecular:381.9L-Ascorbic acid sodium salt
CAS: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.Fórmula:C6H7NaO6Pureza:98.73% - 99.75%Cor e Forma:Less Solid PowderPeso molecular:198.11SN 6
CAS:SN 6 (SN6) is a selective Na+/Ca2+ exchanger (NCX) inhibitor (IC50s of NCX1: 2.9 μM , NCX2: 16 μM ,NCX3: 8.6 μM)Fórmula:C20H22N2O5SPureza:97.28%Cor e Forma:SolidPeso molecular:402.46ZSET1446
CAS:ZSET1446 (ST-101) is a T-type calcium channel activator potentially for the treatment of learning deficits in various types of Alzheimer disease (AD) models.Fórmula:C15H12N2OPureza:99.32%Cor e Forma:SolidPeso molecular:236.27Ref: TM-T8448
1mg52,00€5mg108,00€10mg153,00€25mg298,00€50mg432,00€100mg605,00€200mg815,00€1mL*10mM (DMSO)126,00€Menthol
CAS:Menthol (DL-Menthol) is an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties.Fórmula:C10H20OPureza:99.84% - 99.88%Cor e Forma:White Crystals /89-78-1/ Physical Description White Crystalline Solid With A Peppermint Odor And Taste (Ntp 1992)Peso molecular:156.2614-Deoxyandrographolide
CAS:14-Deoxyandrographolide is a bioactive compound of Andrographis paniculata with hepatoprotective efficacy.Fórmula:C20H30O4Pureza:99.89% - 99.98%Cor e Forma:SolidPeso molecular:334.45Cinacalcet metabolite M4
CAS:<p>Cinacalcet metabolite M4 (Rarechem AL BW 1078) is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.</p>Fórmula:C10H12F3NPureza:97.13%Cor e Forma:SolidPeso molecular:203.2Tetrandrine
CAS:Tetrandrine (Sinomenine A) is a naturally occurring biphenylisoquinoline alkaloid, a calcium channel inhibitor. Cost-effective and quality-assured.Fórmula:C38H42N2O6Pureza:99.61% - 99.94%Cor e Forma:White SolidPeso molecular:622.75Apinocaltamide
CAS: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.Fórmula:C22H18F3N5OPureza:99.80%Cor e Forma:SolidPeso molecular:425.41N6-(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%Cor e Forma:SolidPeso molecular:311.29Bupivacaine
CAS:Bupivacaine (AH-250) is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channelsFórmula:C18H28N2OPureza:99.83%Cor e Forma: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%Cor e Forma:White To Pale Yellow Crystalline PowderPeso molecular:524.95Diltiazem
CAS: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.Fórmula:C22H26N2O4SPureza:99.51% - 99.83%Cor e Forma:White Crystalline Powder SolidPeso molecular:414.52Equilin
CAS:Equilin (7-Dehydroestrone) is a neurotrophic estrogenic steroid with vasodilatory activity used in the study of hypertension.Fórmula:C18H20O2Pureza:98.57% - 99.72%Peso molecular:268.35Bupivacaine-d9
CAS: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.Fórmula:C18H19D9N2OCor e Forma:SolidPeso molecular:297.48Gabapentin enacarbil
CAS:Gabapentin enacarbil (XP-13512) is a prodrug for the anticonvulsant and analgesic gabapentin, offering sustained dose-proportional exposure and predictable bioavailability.Fórmula:C16H27NO6Pureza:99.31%Cor e Forma:SolidPeso molecular:329.39Ref: TM-T15366
1mg42,00€5mg88,00€10mg127,00€25mg274,00€50mg439,00€100mg705,00€200mg938,00€1mL*10mM (DMSO)87,00€1-tert-Butyl 3-Ethyl 5-methyl 2-((2-((tert-Butoxycarbonyl)amino)ethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-1,3,5(4H)-tricarboxylate
CAS:Produto 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:C30H41ClN2O9Cor e Forma:NeatPeso molecular:609.1074-(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
Produto 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:C17H17ClN2O4Cor e Forma:NeatPeso molecular:348.781Cinepazide
CAS:Cinepazide: a vasodilator targeting adenosine A2 receptors, treats various vascular diseases.Fórmula:C22H31N3O5Cor e Forma:White PowderPeso molecular:417.5Amlodipine besilate impurity G
CAS:Amlodipine besilate impurity G is a Calcium Channel antagonist with potential application in the study of neurological diseases and is an impurity in theFórmula:C17H18ClNO4Pureza:98%Cor e Forma:SolidPeso molecular:335.78Amlodipine hydrochloride
CAS:Amlodipine hydrochloride is a salt of Amlodipine --- a medication used to lower blood pressure and prevent chest pain.Fórmula:C20H26Cl2N2O5Cor e Forma:SolidPeso molecular:445.34Nifedipine-d6
CAS:<p>Nifedipine D6 is deuterium labeled nifedipine which is a potent blocker of calcium channel.</p>Fórmula:C17H18N2O6Pureza:98%Cor e Forma:SolidPeso molecular:352.37Topiramate D12
CAS:Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.Fórmula:C12H21NO8SPureza:98%Cor e Forma:SolidPeso molecular:351.44Cinnarizine D8
CAS:Cinnarizine D8 is a deuterium-labeled Cinnarizine which is an antihistamine and a calcium channel blocker.Fórmula:C26H28N2Pureza:98%Cor e Forma:SolidPeso molecular:376.573Maresin 1
CAS:Maresin 1 is biosynthesized by macrophages (MΦ) and possesses significant anti-inflammatory activity that attenuates LPS-induced lung injury in mice.Fórmula:C22H32O4Cor e Forma:SolidPeso molecular:360.49Ionomycin 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%Cor e Forma:SolidPeso molecular:747.07ORM-10103
CAS: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 nMFórmula:C20H16N2O4Pureza:99.9%Cor e Forma:SolidPeso molecular:348.35Ref: TM-T12321
1mg43,00€5mg90,00€10mg135,00€25mg278,00€50mg445,00€100mg605,00€200mg817,00€1mL*10mM (DMSO)90,00€R-(-)-Niguldipine hydrochloride
CAS:R-(-)-Niguldipine HCl: L-type Ca2+ blocker, K+ agonist, α1A antagonist; lowers blood pressure; weaker enantiomer.Fórmula:C36H40ClN3O6Cor e Forma:SolidPeso molecular:646.17Falipamil
CAS:Produto 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:C24H32N2O5Cor e Forma:NeatPeso molecular:428.52(S)-Lercanidipine Hydrochloride
CAS:Produto ControladoFórmula:C36H41N3O6·ClHCor e Forma:NeatPeso molecular:648.19Dihydrocinnamyl Cilnidipine
Produto 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:C27H30N2O7Cor e Forma:NeatPeso molecular:494.543-Desethyl-3-(2-phthalimidoethyl) Phthaloyl Amlodipine
Produto 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:C36H30ClN3O9Cor e Forma:NeatPeso molecular:684.091(R)-Lercanidipine Hydrochloride
CAS:Produto ControladoFórmula:C36H41N3O6·ClHCor e Forma:NeatPeso molecular:648.19Halofuginone
CAS:Halofuginone (RU-19110) inhibits prolyl-tRNA synthetase (Ki=18.3 nM), down-regulates Smad3, and blocks TGF-β at 10 ng/ml.Fórmula:C16H17BrClN3O3Pureza:99.53%Cor e Forma:Off-White SolidPeso molecular:414.68Ref: TM-T6856
1mg37,00€5mg87,00€10mg123,00€25mg240,00€50mg363,00€100mg547,00€500mg1.198,00€1mL*10mM (DMSO)A consultarVerapamil
CAS:Verapamil (CP-16533-1), an oral calcium channel blocker, inhibits P-gp and CYP3A4, used for hypertension, arrhythmias, and angina research.Fórmula:C27H38N2O4Pureza:99.61% - 99.93%Cor e Forma:OilPeso molecular:454.6Ref: TM-T20656
10mg35,00€25mg51,00€50mg73,00€100mg96,00€200mg143,00€500mg230,00€1mL*10mM (DMSO)55,00€Aladorian
CAS:Aladorian (ARM036), a benzothiazepine, has anti-arrhythmic properties for heart failure and CPVT research.Fórmula:C12H13NO4SPureza:98%Cor e Forma:SolidPeso molecular:267.3Aprindine hydrochloride
CAS:Aprindine HCl, a Class 1b antiarrhythmic, treats heart arrhythmias, outperforming digoxin in delaying atrial fibrillation. It's effective orally.Fórmula:C22H31ClN2Cor e Forma:SolidPeso molecular:358.95Levamlodipine gentisate
CAS:Levamlodipine gentisate, an active amlodipine enantiomer, is a dihydropyridine calcium channel blocker for treating hypertension and angina.Fórmula:C27H31ClN2O9Pureza:98%Cor e Forma:SolidPeso molecular:563Ethacrynate Sodium
CAS:Ethacrynate Sodium, a sodium salt, blocks chloride, potassium, and sodium transport mainly in Henle's loop.Fórmula:C13H12Cl2NaO4Pureza:98%Cor e Forma:SolidPeso molecular:326.12JTV-519 hemifumarate
CAS:JTV-519 hemifumarate: Ca2+ blocker, SERCA inhibitor, ryanodine receptor partial agonist; antiarrhythmic, cardioprotective.Fórmula:C54H68N4O8S2Pureza:98%Cor e Forma:SolidPeso molecular:965.28JTV-519
CAS: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) byFórmula:C25H33ClN2O2SPureza:99.88%Cor e Forma:SolidPeso molecular:461.06Ref: TM-T24239
1mg60,00€5mg110,00€10mg155,00€25mg248,00€50mg365,00€100mg545,00€500mg1.188,00€1mL*10mM (DMSO)134,00€S-312-d
CAS:S-312d is a calcium channel antagonist. S-312-d can offer marked neuronal protective effects against ischemic injury.Fórmula:C20H22N2O4SPureza:98%Cor e Forma:SolidPeso molecular:386.46UK-52831
CAS:UK-52831, a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.Fórmula:C22H26Cl2N6O5Pureza:98%Cor e Forma:SolidPeso molecular:525.39Niguldipine 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:CGP 28392 is used as a partial calcium channel agonist.Fórmula:C18H17F2NO5Pureza:98%Cor e Forma:SolidPeso molecular:365.33Kadethrin
CAS:Kadethrin is a synthetic pyrethroid. It was used as a pesticide.Fórmula:C23H24O4SPureza:98%Cor e Forma:Yellow-Brown Viscous Oil SolidPeso molecular:396.5N-Salicyloyltryptamine
CAS:N-Salicyloyltryptamine (STP): a tryptamine with anticonvulsant, anti-inflammatory, analgesic effects; inhibits Na+, Ca2+, K+ channels (IC50 34.6 μM).Fórmula:C17H16N2O2Cor e Forma:SolidPeso molecular:280.32YS-035 hydrochloride
CAS:inhibitor of outward K+ currentsFórmula:C21H30ClNO4Pureza:98%Cor e Forma:SolidPeso molecular:395.92Norbormide
CAS:Norbormide is a toxic compound used as a rodenticide. It has several mechanisms of action, acting as a vasoconstrictor and calcium channel blocker.Fórmula:C33H25N3O3Pureza:98%Cor e Forma:Crystals From Methylene Chloride + Ether Norbormide Is A Colorless To Off-White Crystalline Powder Used As A Selective Rat Poison (Epa 1998)Peso molecular:511.57Anipamil
CAS:Anipamil is a long-acting blocker of calcium channel,and for the treatment of cardiovascular disease.Fórmula:C34H52N2O2Pureza:98%Cor e Forma:SolidPeso molecular:520.79(S)-Lercanidipine hydrochloride
CAS:(S)-Lercanidipine hydrochloride is the S-enantiomer of Lercanidipine hydrochloride. (S)-lercanidipine hydrochloride is a potent blocker of calcium channel.Fórmula:C36H42ClN3O6Pureza:98%Cor e Forma:SolidPeso molecular:648.19SOCE inhibitor 1
CAS:SOCE inhibitor 1 is a inhibitor of store-operated calcium entry (SOCE)(IC50 of 4.4 μM).Fórmula:C25H22F3N5O4Pureza:98%Cor e Forma:SolidPeso molecular:513.47GSK-5498A
CAS:GSK-5498A: Selective CARC blocker, inhibits release of mediators from mast cells and cytokines from T-cells (IC50, 1 μM).Fórmula:C18H11F6N3OCor e Forma:SolidPeso molecular:399.29Lemildipine
CAS:Lemildipine is a new blocker of dihydropyridine calcium entry.Fórmula:C20H22Cl2N2O6Cor e Forma:SolidPeso molecular:457.3GSK-5503A
CAS:GSK-5503A is a novel channel blocker of CRAC.Fórmula:C23H17F2N3O2Pureza:98%Cor e Forma:SolidPeso molecular:405.4ORM-10962
CAS: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 55Fórmula:C27H29N3O4Pureza:98%Cor e Forma:SolidPeso molecular:459.54PD-217014 HCl
CAS:PD-217014, a GABA analog, blocks (3)H-gabapentin on alpha(2)delta calcium channels (K(i) 18 nmol/l), and is a visceral analgesic.Fórmula:C11H19NO2Pureza:98%Cor e Forma:SolidPeso molecular:197.27A 39355
CAS:A 39355 may specifically overcome multidrug resistance without the serious hypotensive effects associated with calcium antagonists.Fórmula:C28H39Cl2N3OPureza:98%Cor e Forma:SolidPeso molecular:504.54NP-252
CAS:NP-252 is a calcium channel antagonist potentially for the treatment of angina pectoris and congestive heart failure.Fórmula:C26H35N3O5Pureza:98%Cor e Forma:SolidPeso molecular:469.57KB-130015
CAS:KB-130015, a activator of hERG1 potassium channels, blocks native and recombinant hERG1 channels at high voltages.Fórmula:C18H14I2O4Pureza:98%Cor e Forma:SolidPeso molecular:548.11Watanidipine dihydrochloride
CAS:Watanidipine dihydrochloride is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.Fórmula:C41H44Cl2N4O6Pureza:98%Cor e Forma:SolidPeso molecular:759.73Gallopamil, (-)-
CAS:Gallopamil, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.Fórmula:C28H40N2O5Pureza:98%Cor e Forma:SolidPeso molecular:484.63AK-2-38
CAS:AK-2-38 is a nifedipine analogue with potent smooth muscle calcium antagonist action and partial agonist effects on isolated guinea pig left atrium.Fórmula:C26H30N2O4Pureza:98%Cor e Forma:SolidPeso molecular:434.53Falipamil
CAS:Falipamil, a verapamil derivative, is a calcium channel blocker with antitachycardic and potential antianginal effects.Fórmula:C24H32N2O5Pureza:98%Cor e Forma:SolidPeso molecular:428.52Tiropramide
CAS:Tiropramide is an antispasmodic drug. It also useful to inhibit the contractile response of the urinary bladder and in managing abdominal pain in IBS.Fórmula:C28H41N3O3Pureza:98%Cor e Forma:SolidPeso molecular:467.64Bms 188107
CAS:Bms 188107 is a calcium antagonist, it has cardioprotective effects.Fórmula:C25H26N2O4Pureza:98%Cor e Forma:SolidPeso molecular:418.48AZD 2066
CAS:AZD 2066 is a selective, orally active, and brain-penetrant mGluR5 antagonist with analgesic activity.Fórmula:C19H16ClN5O2Pureza:98%Cor e Forma:SolidPeso molecular:381.82BBR 2160
CAS:BBR 2160: a calcium-antagonist dihydropyridine derivative, reduces heart tissue contractility and shortens action potentials.Fórmula:C21H25N3O7SCor e Forma:SolidPeso molecular:463.5Ronipamil
CAS:Ronipamil is an analogue of verapamil that used as a calcium entry blocker.Fórmula:C32H48N2Cor e Forma:SolidPeso molecular:460.74Lercanidipine, (S)-
CAS:(S)-Lercanidipine: a dihydropyridine calcium blocker with prolonged antihypertensive and kidney-protective properties.Fórmula:C36H41N3O6Pureza:98%Cor e Forma:SolidPeso molecular:611.73Riodipine
CAS:Riodipine, a calcium channel blocker, is used as cardiovascular drugs.Fórmula:C18H19F2NO5Pureza:98%Cor e Forma:SolidPeso molecular:367.34Hexadecylphosphoserine
CAS:Hexadecylphosphoserine is a representative growth inhibitor.Fórmula:C19H40NO6PPureza:98%Cor e Forma:SolidPeso molecular:409.5SB-237376 HCl
CAS:SB-237376 HCl (SB-237376 hydrochloride) is a calcium and potassium channel antagonist used in the treatment of cardiac arrhythmias.Fórmula:C20H26ClN3O5Pureza:98.70%Cor e Forma:SolidPeso molecular:423.89Dopropidil hydrochloride
CAS:Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris.Fórmula:C20H36ClNO2Cor e Forma:SolidPeso molecular:357.96SCH00013
CAS:SCH00013 is a cardiotonic that enhances myofibrillar Ca++ sensitivity, with notable effects at pH 7.2-7.4.Fórmula:C18H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:324.38GZ4
CAS:GZ4 is a Ca2+ currents inhibitor, acting on cell surface channels.Fórmula:C11H17NO2Pureza:98%Cor e Forma:SolidPeso molecular:195.26BN 50341
CAS:BN 50341 is an inhibitor of antithrombotic platelet activating factor.Fórmula:C32H41ClN2O4Pureza:98%Cor e Forma:SolidPeso molecular:553.13EO-122
CAS:EO-122, a calcium channel antagonist and sodium channel antagonist, is used potentially for the treatment of arrhythmia.Fórmula:C16H23ClN2OCor e Forma:SolidPeso molecular:294.82Gallopamil HCl, (-)-
CAS:Gallopamil HCl, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.Fórmula:C28H41ClN2O5Pureza:98%Cor e Forma:SolidPeso molecular:521.09Hns 32
CAS:Hns 32 possesses antiarrhythmic properties in dog and guinea pig hearts. It also has vasodilator action.Fórmula:C24H29N3Pureza:98%Cor e Forma:SolidPeso molecular:359.51A 80b
CAS:A-80b: synthetic pyridazinoindole; potent, lasting antihypertensive; lowers diastolic more; no change in heart rate; inhibits Ca2+-induced contraction.Fórmula:C16H17N7Pureza:98%Cor e Forma:SolidPeso molecular:307.35Methsuximide
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:203.243',4'-Dichlorobenzamil HCl
CAS:3',4'-Dichlorobenzamil HCl is an inhibitor of Na+ transport, Na+/Ca2+ exchanger, sarcoplasmic reticulum Ca2+ release channels.Fórmula:C13H12Cl3N7OPureza:98%Cor e Forma:Yellow SolidPeso molecular:388.64BAY-Y-5959
CAS:BAY-Y-5959, a calcium channel agonist, is used potentially for the treatment of arrhythmia, heart failure and myocardial.Fórmula:C26H24N4O2Cor e Forma:SolidPeso molecular:424.49SM-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 cerebrovascularFórmula:C26H27N5O5Pureza:99.43%Cor e Forma:SolidPeso molecular:489.52trans-Ned 19
CAS:trans-Ned 19 blocks NAADP and TPC, hindering calcium signaling and aorta relaxation at low histamine levels.Fórmula:C30H31FN4O3Pureza:98%Cor e Forma:SolidPeso molecular:514.59Ricinelaidic Acid
CAS:Ricinelaidic acid blocks LTB4 receptors; hampers human neutrophil responses; reduces rat bronchoconstriction by 46% at 1 mg/kg i.v.Fórmula:C18H34O3Cor e Forma:SolidPeso molecular:298.46Diproteverine
CAS:Diproteverine is a calcium antagonist, it has antianginal property.Fórmula:C26H35NO4Pureza:98%Cor e Forma:SolidPeso molecular:425.56BMS-192364
CAS:BMS-192364 is a bio-active chemical.Fórmula:C15H9ClF3N3O2Cor e Forma:SolidPeso molecular:355.70Mci 176
CAS:Mci 176 is a quinazolinone calcium antagonist.Fórmula:C24H32ClN3O4Cor e Forma:SolidPeso molecular:461.98BA 41899
CAS:BA 41899 is a positive inotropic Ca(2+)-sensitizing agent.Fórmula:C18H16N2O2Cor e Forma:SolidPeso molecular:292.33MRS2690
CAS:MRS2690 is a potent P2Y14 receptor agonist (EC50 = 49 nM) that displays 7-fold higher potency than UDP-glucose.Fórmula:C15H24N2O16P2SCor e Forma:SolidPeso molecular:582.37SIM-6080
CAS:SIM-6080 is a calcium channel antagonist. SIM-6080 inhibits the proliferation of rat aortic myocytes.Fórmula:C29H36F2N2O3Cor e Forma:SolidPeso molecular:498.6RS-93522
CAS:RS-93522: Calcium channel antagonist, inhibits phosphodiesterase (IC50=1.6x10^-5M), like milrinone, and has a negative inotropic effect.Fórmula:C27H30N2O9Pureza:98%Cor e Forma:SolidPeso molecular:526.54Hyperforin dicyclohexylammonium salt
CAS:Hyperforin dicyclohexylammonium is a TRPC6 activator and antidepressant that modulates Ca2+ levels.Fórmula:C47H75NO4Pureza:98%Cor e Forma:SolidPeso molecular:718.10AJG-049 free base
CAS:AJG-049 free base is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).Fórmula:C27H30N2O2Cor e Forma:SolidPeso molecular:414.54Azelnidipine, (S)-
CAS:Azelnidipine, a selective L-type CCB, improves HF severity and cardiac function in HT and HFpEF compared to N-type CCB cilnidipine.Fórmula:C33H34N4O6Cor e Forma:SolidPeso molecular:582.65YM 244769 hydrochloride
CAS:inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)Fórmula:C26H23ClFN3O3Pureza:98%Cor e Forma:SolidPeso molecular:479.93TTA-Q6(isomer)
CAS:TTA-Q6(isomer) is an isomer of TTA-Q6. TTA-Q6 is a selective antagonist of the T-type Ca2+ channel.Fórmula:C20H15ClF3N3OPureza:98%Cor e Forma:SolidPeso molecular:405.8PPZ2
CAS:PPZ2 is a novel DAG-activated TRPC3/TRPC6/TRPC7 channels activator.Fórmula:C22H29N3O2Cor e Forma:SolidPeso molecular:367.48Aladorian sodium
CAS:Aladorian sodium is used for Treatment of Cardiovascular Diseases.Fórmula:C12H13NNaO4SCor e Forma:SolidPeso molecular:290.29Flordipine
CAS:Flordipine is used as a calcium channel blocker.Fórmula:C26H33F3N2O5Pureza:98%Cor e Forma:SolidPeso molecular:510.55YS-201
CAS:YS-201 is an antagonist of dihydropyridine-type calcium channel.Fórmula:C24H31N3O6Pureza:98%Cor e Forma:SolidPeso molecular:457.52PAQ
CAS:PAQ protects neurons in Parkinson's models at 10 μM; prevents neuron loss in mice substantia nigra with 25-50 mg/kg doses.Fórmula:C14H11N3Cor e Forma:SolidPeso molecular:221.26Topiramate lithium
CAS:Topiramate lithium: antiepileptic, GluR5 antagonist, enhances GABA, inhibits kainate/AMPA, Na+/Ca2+ channels; ↑ K+ conductance; ↓ carbonic anhydrase.Fórmula:C12H20LiNO8SCor e Forma:SolidPeso molecular:345.29Ro 18-3981
CAS:Ro 18-3981 inhibits myocardial Ca2+ channels; KD is 1.0 nM, close to IC50 for ICa block (2.3 nM).Fórmula:C24H33N3O8SCor e Forma:SolidPeso molecular:523.6Azelnidipine, (R)-
CAS:Azelnidipine is an L-type CCB that improves HF severity and cardiac nerve activity in HT and HFpEF compared to cilnidipine.Fórmula:C33H34N4O6Cor e Forma:SolidPeso molecular:582.65PD 122860
CAS:PD 122860 is a dihydropyridine enhancing heart contractility, altering ECG, and relaxing aortic rings.Fórmula:C23H20F3N3O4SPureza:98%Cor e Forma:SolidPeso molecular:491.48SR-33805
CAS:SR-33805: calcium channel blocker for atherosclerosis/heart failure, enhances myocyte function, modulates myofilament phosphorylation.Fórmula:C32H40N2O5SCor e Forma:SolidPeso molecular:564.74TTA-Q6
CAS: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.Fórmula:C20H15ClF3N3OPureza:99.97%Cor e Forma:SolidPeso molecular:405.8Teludipine hydrochloride
CAS:Teludipine hydrochloride is a blocker of lipophilic calcium channel.Fórmula:C28H39ClN2O6Pureza:98%Cor e Forma:SolidPeso molecular:535.07AE0047 Hydrochloride
CAS:AE0047 Hydrochloride is a blocker of calcium, and used in the research of the hypertensive disease.Fórmula:C41H43ClN4O6Pureza:98%Cor e Forma:SolidPeso molecular:723.26AZD-2066 hydrochloride
CAS:AZD-2066 hydrochloride is an mGlu5 antagonist.Fórmula:C19H17Cl2N5O2Cor e Forma:SolidPeso molecular:418.28BK 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:392.53Palonidipine HCl
CAS:Palonidipine HCl is a calcium channel antagonist potentially for the treatment of angina pectoris and hypertension.Fórmula:C29H35ClFN3O6Cor e Forma:SolidPeso molecular:576.06Dehydronitrosonisoldipine
CAS:Dehydronitrosonisoldipine blocks SARM1, slows axon decay & cADPR synthesis; useful in neurodegeneration research.Fórmula:C20H22N2O5Pureza:99.68%Cor e Forma:SolidPeso molecular:370.4Ref: TM-T10991
1mg52,00€2mg80,00€5mg131,00€10mg177,00€25mg305,00€50mg437,00€100mg562,00€500mg1.121,00€1mL*10mM (DMSO)129,00€Levosemotiadil
CAS:Levosemotiadil（SA 3212） is a novel calcium antagonist and a very potent inhibitor of low-density lipoprotein oxidation.Levosemotiadil may be used to preventFórmula:C29H32N2O6SPureza:98.53% - 98.88%Cor e Forma:SolidPeso molecular:536.64(R)-Amlodipine
CAS:(R)-Amlodipine is the R-enantiomer of Amlodipine and functions as an orally active dihydropyridine calcium channel blocker with antianginal properties.Fórmula:C20H25ClN2O5Pureza:99.977%Cor e Forma:SolidPeso molecular:408.88Diltiazem malate
CAS:Diltiazem malate is an ACE inhibitor and non-dihydropyridine calcium channel blocker used in the treatment of hypertension.Fórmula:C26H32N2O9SCor e Forma:SolidPeso molecular:548.60ML218 hydrochloride
CAS:ML218 hydrochloride inhibits T-type Ca2+ channels Cav3.1-3.3; most effective on Cav3.2 and Cav3.3 (IC50s: 310 nM, 270 nM).Fórmula:C19H27Cl3N2OPureza:98%Cor e Forma:SolidPeso molecular:405.79ITH-12575
CAS:ITH-12575 is an inhibitor of Mitochondrial Na+/Ca2+ exchange (mNCX). ITH12575 reduces Ca(2+) influx through CALHM1 at low micromolar concentrations.Fórmula:C18H18ClNOSCor e Forma:SolidPeso molecular:331.86RS 30026
CAS:RS 30026 is a potent calcium channel agonist.Fórmula:C23H21NO4SCor e Forma:SolidPeso molecular:407.48CaV1.3 antagonist-1
CAS:CaV1.3 antagonist-1 is a selective CaV1.3L-type calcium channel antagonist useful for researching neurological disorders and cardiovascular diseases.Fórmula:C17H19ClN2O3Cor e Forma:SolidPeso molecular:334.8NC 1100
CAS:NC 1100 is a calcium channel antagonist.Fórmula:C27H34Cl2N2O3Pureza:98%Cor e Forma:SolidPeso molecular:505.48
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