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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Diproteverine
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
