santa cruz biotechnology, inc.

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| | Chloride Channel Modulators
- 9-AC
Cl- transport inhibitor with a moderate to strong inhibitory action on PKA activated cardiac IcI.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203483 | 723-62-6 | C15H10O2 | 100 mg |
- DPC
A potent, non-specific blocker of Cl– channel and chloride-bicarbonate exchange. Also inhibits cystic fibrosis transmembrane regulator (CFTR) ATPase activity. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202590 | 91-40-7 | C13H11NO2 | 1 g |
- DCPIB
Selective blocker of VSAC/ICl, swell in various CV tissues; inhibits glucose-stimulated insulin release. In vitro, reverses cell swelling-induced action potential duration shortening in atrial myocytes and inhibits astroglial swelling.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203913 | 82749-70-0 | C22H28Cl2O4 | 10 mg/50 mg |
- DCEBIO
Stimulates the secretion of Cl- via activation of hIK1 K+ channels and the activation of an apical Cl- conductance. Is more potent than its analog 1-EBIO| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203561 | 60563-36-2 | C9H8Cl2N2O | 10 mg/50 mg |
- DIDS, Disodium Salt
Binds covalently and irreversibly to the outer surface of human erythrocyte membranes. Inhibits ATP transport into endoplasmic reticulum vesicles. Anion transport inhibitor that inhibits Cl– uptake (IC50 = 150 nM) in neuroblastoma cells. Has anti-ulcerous properties.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203919 | 67483-13-0 | C16H8Na2N2O6S4 | 250 mg/25 mg/100 mg |
- Fipronil
A channel blocker that blocks GABA-gated chloride channels and glutamate-activated chloride channels (GluCls). | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201546 | 120068-37-3 | C12H4Cl2F6N4OS | 20 mg/100 mg |
- IAA-94
A potent mammalian skeletal muscle and epithelial Cl- channel blocker (Ki=1µM in bovine kidney cortex microsomes). | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201544 | 54197-31-8 | C17H18Cl2O4 | 10 mg/50 mg |
- Lonidamine
An indazole compound that has been reported to inhibit angiogenic-related endothelial cell functions. Also been shown to cause a decrease in proliferation, migration, and morphogenesis of cells.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203115 | 50264-69-2 | C15H10Cl2N2O2 | 5 mg/25 mg |
- 5-Nitro-2-(3-phenylpropylamino)benzoic Acid (NPPB)
A potent chloride channel blocker. Shown to suppress prostaglandin E2 release.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201542 | 107254-86-4 | C16H16N2O4 | 10 mg/50 mg |
- PG 01
A cystic fibrosis transmembrane conductance regulator (CFTR) potentiator which is reported to correct gating defects of several CFTR mutants.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-358839 | 853138-65-5 | C28H29N3O2 | 10 mg/50 mg |
- Picrotoxin
A noncompetitive inhibitor of GABA Cl--current which affects neuronal firing activity. Shown to increase noradrenaline levels and turnover in the hypothalamus.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202765 | 124-87-8 | C30H34O13 | 1 g/5 g |
- SFK1
A cell permeable suppressor of FK506 1, which, in high salt media, reverses the inhibition of cell growth by FK506. It interacts with Por1p (YVDAC1) channel protein in the outer mitochondrial membrane. The compound perturbs ion homeostasis and induces hyperpolarization of the inner mitochondrial membrane and mitochondria-dependent cell death with ROS (reactive oxygen species) production in a low NaCl growth media. It also induces expression of calcineurin targeted genes. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-215849 | 678997-25-6 | C23H36N2O2•HCl | 10 mg |
- Talniflumate
Calcium-activated chloride channel (hCLCA1/mCLCA3) blocker that reduces mucin synthesis and release in animal models and cell culture. Possesses anti-inflammatory actions via inhibition of cyclooxygenases and inhibits Cl-/HCO3- exchanger activity. Increases survival in a cystic fibrosis mouse model of distal intestinal obstructive syndrome.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203706 | 66898-62-2 | C21H13F3N2O4 | 10 mg/50 mg |
- VRT-532
A mutated G551D CFTR corrector. VRT-532 mediates G551D-CFTR by enhancing ATP affinity of the mutant. VRT-532 also potentiates F508del mutated CFTR and works specifically on mutant CFTR rather than other membrane proteins.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-253832 | 38214-71-0 | C16H14N2O | 5 mg |
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