
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:631.66HA-1004 HCl
CAS:HA-1004 is an inhibitor of PKA, cGKI, PKC, MYLK, and calcium channel protein.Fórmula:C12H17Cl2N5O2SCor e Forma:SolidPeso molecular:366.27Bepridil hydrochloride
CAS:Bepridil hydrochloride (CERM 1978) is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX), sodium channels and cardiac sarcolemmal KATP channelsFórmula:C24H35ClN2OPureza:99.45% - 99.68%Cor e Forma:SolidPeso molecular:4032,5-Di-tert-butylhydroquinone
CAS:2,5-Di-tert-butylhydroquinone (BHQ) is an effective and selective endoplasmic reticulum Ca2+-ATPase inhibitor.Fórmula:C14H22O2Pureza:97.11%Cor e Forma:PelletslargecrystalsPeso molecular:222.32DHBP dibromide
CAS:DHBP dibromide (1,1'-DI-N-HEPTYL-4,4'-BIPYRIDINIUM DIBRO) is calcium release and a muscle relaxant inhibitor.Fórmula:C24H38Br2N2Pureza:99.73%Cor e Forma:Yellow To Yellow-Green Powder Or FlakesPeso molecular:514.38GSK1016790A
CAS:GSK1016790A (GSK101) (GSK101) is a novel, potent activator of TRPV4 (transient receptor potential vanilloid 4) with EC50 of 34 nM in choroid plexus epithelialFórmula:C28H32Cl2N4O6S2Pureza:97.37% - 99.38%Cor e Forma:SolidPeso molecular:655.61Propiverine hydrochloride
CAS:Propiverine is a widely used antimuscarinic drug with a mixed mode of action in the treatment of symptoms associated with overactive bladder (OAB).Fórmula:C23H30ClNO3Pureza:99.93%Cor e Forma:White Crystalling PowerPeso molecular:403.94L-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:165.19(±)-Praeruptorin A
CAS:(±)-Praeruptorin A could exhibit its anti-osteoclastogenic activity by inhibiting p38/Akt-c-Fos-NFATc1 signaling and PLCγ-independent Ca(2+) oscillation.Fórmula:C21H22O7Pureza:98.9% - 99.73%Cor e Forma:SolidPeso molecular:386.40(+)-Kavain
CAS:(+)-Kavain ((R)-KAWAIN) is one of the six major kavalactones found in the Piper methysticum (kava) plant; reversible inhibitor of MAO-B.Fórmula:C14H14O3Pureza:97% - ≥95%Cor e Forma:White Fine PowderPeso molecular:230.26Suvecaltamide
CAS:Suvecaltamide (MK-8998) as potent inhibitors of T-type calcium channels.Fórmula:C20H23F3N2O2Pureza:99.29% - 99.70%Cor e Forma:SolidPeso molecular:380.4SR33805
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:564.74NS-638
CAS:NS-638 is a Ca2+-channel blocker. It can block K+-stimulated intracellular Ca2+-elevation (IC50: 3.4 μM).Fórmula:C15H11ClF3N3Pureza:98.44%Cor e Forma:SolidPeso molecular:325.72Efonidipine hydrochloride monoethanolate
CAS:Efonidipine HCl monoethanolate is a calcium blocker, boosts dehydroepiandrosterone sulfate in NCI-H295R cells.Fórmula:C36H45ClN3O8PPureza:>99.99%Cor e Forma:SolidPeso molecular:714.18Praeruptorin 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:428.47Ibutilide Fumarate
CAS:Ibutilide Fumarate is a class III antiarrhythmic, prolonging action potentials by enhancing sodium influx, and can extend QT interval.Fórmula:(C20H36N2O3S)2·C4H4O4Pureza:99.68% - 99.74%Cor e Forma:SolidPeso molecular:885.23Argireline
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:888.99Azumolene 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:371.13S107
CAS:S107 stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.Fórmula:C11H15NOSPureza:99.90%Cor e Forma:SolidPeso molecular:209.31TGR5 Receptor Agonist
CAS:TGR5 is a potent TGR5(GPCR19) agonist.Fórmula:C18H14Cl2N2O2Pureza:99.77% - ≥95%Cor e Forma:SolidPeso molecular:361.22
