santa cruz biotechnology, inc.

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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 Nummer | Summenformel | Menge |
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| sc-203794 | 79127-24-5 | C20H29ClN2O2S ·HCl | 10 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 Nummer | Summenformel | Menge |
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| sc-201494 | 57265-65-3 | C31H23Cl6N2O··Cl | 10 mg/50 mg |
- CGS 9343B
Calmodulin antagonist that inhibits calmodulin-stimulated cAMP phosphodiesterase activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203883 | 109826-27-9 | C26H28N4O2 ·C4H4O4 | 10 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 Nummer | Summenformel | Menge |
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| sc-221573 | 73885-53-7 | C44H43N3O9 | 10 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 Nummer | Summenformel | Menge |
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| sc-201502 | 83016-35-7 | C22H25ClF3N3S ·2HCl | 50 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 Nummer | Summenformel | Menge |
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| sc-221772 | 187937-24-2 | C18H25IN2O2S•HCl | 5 mg/25 mg |
- Trifluoperazine·2HCl (Stelazine)
A phenothiazine compound with antiadrenergic and antidopaminergic effects.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201498 | 440-17-5 | C21H26Cl2F3N3S | 1 g/5 g |
- Phenoxybenzamine
A cell-permeable, non-specific, irreversible α-adrenergic antagonist that inhibits calmodulin-stimulated phosphodiesterase activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-3581 | 63-92-3 | C18H22ClNO··HCl | 200 mg/1 g |
- W-13 Isomer hydrochloride
Isomer of W-13 | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-222413 | 88519-57-7 | C14H17ClN2O2S ·HCl | 1 mg |
- W-13 Isomer, Decyl Analog hydrochloride
The most potent isomer of the naphthalenesulfonamide family of calmodulin inhibitors.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-222414 | 79127-24-5
| C20H29ClN2O2S ·HCl | 5 mg |
- W-5
A calmodulin antagonist that binds to calmodulin and inhibits calcium-ion-calmodulin- regulated activities.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201500 | 61714-25-8 | C16H22N2O2S ·HCl | 20 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 Nummer | Summenformel | Menge |
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| sc-201501 | 61714-27-0 | C16H21ClN2O2S•HCl | 50 mg |
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