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Calmodulin Inhibitors

  • A-7 hydrochloride
    A potent calmodulin antagonist (inhibits calmodulin-activated PDE activity with an IC50 of 3 μM).
    Katalog #CAS NummerSummenformelMenge
    sc-20379479127-24-5C20H29ClN2O2S ·HCl10 mg
  • Calmidazolium Chloride
    An antagonist of calmodulin and blocker of calmodulin-mediated protein activations. Stimulates Ca2+ entry by a mechanism distinct from store-operated Ca2+ entry in HeLa cells. Demonstrates uncompetitive inhibition of platelet and sarcoplasmic reticulum Ca2+-ATPase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-20149457265-65-3C31H23Cl6N2O··Cl10 mg/50 mg
  • CGS 9343B
    Calmodulin antagonist that inhibits calmodulin-stimulated cAMP phosphodiesterase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-203883109826-27-9C26H28N4O2 ·C4H4O410 mg
  • E6 Berbamine
    A potent, selective, cell-permeable calmodulin antagonist which inhibits calmodulin-dependent enzymes such as MLC kinase (IC50=8 µM) and phosphodiesterase I (IC50=0.53 µM).
    Katalog #CAS NummerSummenformelMenge
    sc-22157373885-53-7C44H43N3O910 mg/50 mg
  • Fluphenazine-N-2-chloroethane・2HCl
    Irreversibly inhibits calmodulin-induced activation of CNPase. Irreversible antagonist of D2 and D1 dopamine receptors.
    Katalog #CAS NummerSummenformelMenge
    sc-20150283016-35-7C22H25ClF3N3S ·2HCl50 mg
  • J-8 hydrochloride
    Highly selective calmodulin (CaM) antagonist. Inhibits Ca2+/calmodulin-dependent phosphodiesterase. Selectivity over Ca2++/CaM-dependent enzymes compared with Ca2+-dependent but CaM-independent enzymes, e.g. protein kinase C (PKC) and transglutaminase.
    Katalog #CAS NummerSummenformelMenge
    sc-221772187937-24-2C18H25IN2O2S•HCl5 mg/25 mg
  • Trifluoperazine·2HCl (Stelazine)
    A phenothiazine compound with antiadrenergic and antidopaminergic effects.
    Katalog #CAS NummerSummenformelMenge
    sc-201498440-17-5C21H26Cl2F3N3S1 g/5 g
  • Phenoxybenzamine
    A cell-permeable, non-specific, irreversible α-adrenergic antagonist that inhibits calmodulin-stimulated phosphodiesterase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-358163-92-3C18H22ClNO··HCl200 mg/1 g
  • W-13 Isomer hydrochloride
    Isomer of W-13
    Katalog #CAS NummerSummenformelMenge
    sc-22241388519-57-7C14H17ClN2O2S ·HCl1 mg
  • W-13 Isomer, Decyl Analog hydrochloride
    The most potent isomer of the naphthalenesulfonamide family of calmodulin inhibitors.
    Katalog #CAS NummerSummenformelMenge
    sc-22241479127-24-5 C20H29ClN2O2S ·HCl5 mg
  • W-5
    A calmodulin antagonist that binds to calmodulin and inhibits calcium-ion-calmodulin- regulated activities.
    Katalog #CAS NummerSummenformelMenge
    sc-20150061714-25-8C16H22N2O2S ·HCl20 mg
  • W-7
    Shown to be a cell permeable calmodulin antagonist that inhibits certain enzyme activities. Also has been reported to be an antiproliferative agent.
    Katalog #CAS NummerSummenformelMenge
    sc-20150161714-27-0C16H21ClN2O2S•HCl50 mg