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 543 produtos de "Canais de Cálcio"
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Maresin 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:360.49Nifedipine-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:352.37Ionomycin 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:494.54(R)-Lercanidipine Hydrochloride
CAS:Produto ControladoFórmula:C36H41N3O6·ClHCor e Forma:NeatPeso molecular:648.193-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:684.091Verapamil
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€Halofuginone
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 consultarFalipamil
CAS:Falipamil, a verapamil derivative, is a calcium channel blocker with antitachycardic and potential antianginal effects.Fórmula:C24H32N2O5Pureza:98%Cor e Forma:SolidPeso molecular:428.52SM-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:489.5218:0 LYSO-PE
CAS: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.Fórmula:C23H48NO7PPureza:98%Cor e Forma:SolidPeso molecular:481.6JTV-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€Halofuginone hydrobromide
CAS:Halofuginone specifically inhibits collagen type I and MMP-2 gene expression, which may result in the suppression of angiogenesis and tumor cell growth.Fórmula:C16H17BrClN3O3·HBrPureza:97.01% - 99.73%Cor e Forma:SolidPeso molecular:495.59Ref: TM-T3524
1mg37,00€2mg52,00€5mg79,00€10mg112,00€25mg219,00€50mg328,00€100mg495,00€500mg947,00€1mL*10mM (DMSO)88,00€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:386.46CXL-1020
CAS:CXL-1020, a HNO prodrug, enhances heart muscle function & relaxation, aiding in heart failure research.Fórmula:C7H9NO5S2Cor e Forma:SolidPeso molecular:251.28Ethacrynate 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:965.28Niguldipine 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:365.33ML218
CAS: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.Fórmula:C19H26Cl2N2OPureza:99.2% - 99.45%Cor e Forma:SolidPeso molecular:369.33UK-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:525.39Tiropramide
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:418.48Kadethrin
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:395.92IDO1-IN-19
CAS:IDO1-IN-19 (Compound 17) is a potent inhibitor of IDO1 and has potential for cancer disease research.Fórmula:C25H22F4N2O3Cor e Forma:SolidPeso molecular:474.45Carboxyamidotriazole
CAS:Carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways.Fórmula:C17H12Cl3N5O2Pureza:98%Cor e Forma:SolidPeso molecular:424.67Norbormide
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:648.19PD0176078
CAS:PD0176078 () is a newly blocker of N-type Calcium channel.Fórmula:C23H30F2N2OPureza:99.72%Cor e Forma:SolidPeso molecular:388.49Ref: TM-T12385
1mg63,00€5mg111,00€10mg180,00€25mg284,00€50mg395,00€100mg543,00€200mg735,00€1mL*10mM (DMSO)138,00€SOCE 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:513.47Leconotide
CAS:Leconotide is a calcium channel blocker and antihyperalgesia agent; isolated from the venom of the cone snail, Conus catus.Fórmula:C107H179N35O36S7Cor e Forma:SolidPeso molecular:2756.23TTA-P2
CAS:TTA-P2: potent CNS-penetrating T-type Ca2+ channel blocker; eliminates Cav3.1 window currents.Fórmula:C21H29Cl2FN2O2Cor e Forma:SolidPeso molecular:431.37GSK-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:399.29Lercanidipine. (R)-
CAS:(R)-Lercanidipine enantiomer: antihypertensive, blocks L-type Ca2+ channels, dilates blood vessels.Fórmula:C36H41N3O6Cor e Forma:SolidPeso molecular:611.73ORM-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:197.27Semotiadil recemate fumarate
CAS:Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel antagonist of vasoselective Ca2+ channel.Fórmula:C33H36N2O10SPureza:98%Cor e Forma:SolidPeso molecular:652.71Lemildipine
CAS:Lemildipine is a new blocker of dihydropyridine calcium entry.Fórmula:C20H22Cl2N2O6Cor e Forma:SolidPeso molecular:457.3trans-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:298.46GSK-5503A
CAS:GSK-5503A is a novel channel blocker of CRAC.Fórmula:C23H17F2N3O2Pureza:98%Cor e Forma:SolidPeso molecular:405.4Diproteverine
CAS:Diproteverine is a calcium antagonist, it has antianginal property.Fórmula:C26H35NO4Pureza:98%Cor e Forma:SolidPeso molecular:425.56Mci 176
CAS:Mci 176 is a quinazolinone calcium antagonist.Fórmula:C24H32ClN3O4Cor e Forma:SolidPeso molecular:461.98Lidoflazine
CAS:Lidoflazine: antianginal, blocks HERG K+ & Ca channels, risks QT prolongation & arrhythmia.Fórmula:C30H35F2N3OPureza:98%Cor e Forma:SolidPeso molecular:491.62BA 41899
CAS:BA 41899 is a positive inotropic Ca(2+)-sensitizing agent.Fórmula:C18H16N2O2Cor e Forma:SolidPeso molecular:292.33BMS-192364
CAS:BMS-192364 is a bio-active chemical.Fórmula:C15H9ClF3N3O2Cor e Forma:SolidPeso molecular:355.70MRS2690
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:498.6(R)-Lercanidipine hydrochloride
CAS:(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.Fórmula:C36H42ClN3O6Pureza:98%Cor e Forma:SolidPeso molecular:648.2RS-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:526.54Sadopine
CAS:Sadopine is a high-affinity radioligand for DHP receptor in L-type Ca2+ channels, suitable for tissue and membrane labeling.Fórmula:C30H40F3N3O7SCor e Forma:SolidPeso molecular:643.71AZD 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:381.82TMB 8 (hydrochloride)
CAS:TMB 8 blocks nAChRs (IC50: 390-480 nM), reduces Ca2+ in muscles, hinders rabbit aorta contraction at 50 μM, and inhibits PKC dose-dependently.Fórmula:C22H38ClNO5Cor e Forma:White SolidPeso molecular:431.99Hyperforin 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:479.93NP-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:469.57β-Amino Acid Imagabalin Hydrochloride
CAS:β-Amino Acid Imagabalin Hydrochloride is the voltage-dependent calcium channel ligand for the α2δ subunit.Fórmula:C9H20ClNO2Pureza:98%Cor e Forma:SolidPeso molecular:209.71NPS-2143
CAS:NPS-2143 (SB 262470A) is a novel potent and selective antagonist of Ca(2+) receptor.Fórmula:C24H25ClN2O2Pureza:99.56%Cor e Forma:SolidPeso molecular:408.92RQ-00311651
CAS:RQ-00311651 is a novel T-type Ca2+ channel blocker. RQ-00311651 also inhibited high K-induced Ca signaling in those cells.Fórmula:C19H18F3N5O2Cor e Forma:SolidPeso molecular:405.37PPZ2
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:290.29TTA-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:405.8PAQ
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:221.26Flordipine
CAS:Flordipine is used as a calcium channel blocker.Fórmula:C26H33F3N2O5Pureza:98%Cor e Forma:SolidPeso molecular:510.55AMG-1
CAS:AMG-1 inhibits CRAC channels, blocks effector T cells, not regulatory ones, and reduces EAE progression.Fórmula:C18H9ClF5N3OCor e Forma:SolidPeso molecular:413.73Ro 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:582.65RyRs activator 3
CAS:RyRs activator 3 (compound A4) serves as an insecticide highly effective against both the diamondback moths, M.Fórmula:C23H19BrCl2N6O3Pureza:98%Cor e Forma:SolidPeso molecular:578.25YS-201
CAS:YS-201 is an antagonist of dihydropyridine-type calcium channel.Fórmula:C24H31N3O6Pureza:98%Cor e Forma:SolidPeso molecular:457.52BBR 2160
CAS:BBR 2160: a calcium-antagonist dihydropyridine derivative, reduces heart tissue contractility and shortens action potentials.Fórmula:C21H25N3O7SCor e Forma:SolidPeso molecular:463.5SR-33805
CAS:SR-33805: calcium channel blocker for atherosclerosis/heart failure, enhances myocyte function, modulates myofilament phosphorylation.Fórmula:C32H40N2O5SCor e Forma:SolidPeso molecular:564.74Topiramate 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:345.29PD 122860
CAS:PD 122860 is a dihydropyridine enhancing heart contractility, altering ECG, and relaxing aortic rings.Fórmula:C23H20F3N3O4SPureza:98%Cor e Forma:SolidPeso molecular:491.48(Rac)-MEM 1003
CAS:MEM-1003, a calcium channel blocker, is used potentially for the treatment of bipolar disorders.Fórmula:C22H25ClN2O5Cor e Forma:SolidPeso molecular:432.9TTA-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:405.8Ronipamil
CAS:Ronipamil is an analogue of verapamil that used as a calcium entry blocker.Fórmula:C32H48N2Cor e Forma:SolidPeso molecular:460.74PD-151307
CAS:PD-151307 is used as an N-type calcium channel blocker.Fórmula:C33H47N3O5Pureza:98%Cor e Forma:SolidPeso molecular:565.74Teludipine hydrochloride
CAS:Teludipine hydrochloride is a blocker of lipophilic calcium channel.Fórmula:C28H39ClN2O6Pureza:98%Cor e Forma:SolidPeso molecular:535.07Lercanidipine, (S)-
CAS:(S)-Lercanidipine: a dihydropyridine calcium blocker with prolonged antihypertensive and kidney-protective properties.Fórmula:C36H41N3O6Pureza:98%Cor e Forma:SolidPeso molecular:611.73AZD-2066 hydrochloride
CAS:AZD-2066 hydrochloride is an mGlu5 antagonist.Fórmula:C19H17Cl2N5O2Cor e Forma:SolidPeso molecular:418.28AJG-049 HCl
CAS:AJG-049 HCl is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).Fórmula:C27H31ClN2O2Cor e Forma:SolidPeso molecular:451.01Palonidipine HCl
CAS:Palonidipine HCl is a calcium channel antagonist potentially for the treatment of angina pectoris and hypertension.Fórmula:C29H35ClFN3O6Cor e Forma:SolidPeso molecular:576.06AE0047 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:723.26Riodipine
CAS:Riodipine, a calcium channel blocker, is used as cardiovascular drugs.Fórmula:C18H19F2NO5Pureza:98%Cor e Forma:SolidPeso molecular:367.34Dehydronitrosonisoldipine
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€Hexadecylphosphoserine
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:423.89Levosemotiadil
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:536.64BK 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:392.53
