 
                Chemical Structure : DCPIB
CAS No.: 82749-70-0
Catalog No.: PC-72941Not For Human Use, Lab Use Only.
DCPIB (SN-401) is a selective, reversible and potent inhibitor of volume-regulated anion channels (VRAC), inhibits TRESK, TASK1 and TASK3 with IC50 of 0.14, 0.95, and 50.72 uM respectively.
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	DCPIB (SN-401) is a selective, reversible and potent inhibitor of volume-regulated anion channels (VRAC), inhibits TRESK, TASK1 and TASK3 with IC50 of 0.14, 0.95, and 50.72 uM respectively.
	DCPIB (SN-401) is a SWELL1 channel inhibitor that bind the SWELL1-LRRC8 channel complexes (IC50=3.9 uM).
	SN-401 increases adipocyte SWELL1 protein expression, and SWELL1-dependent insulin signaling.
	SN-401 increases SWELL1 and improves systemic glucose homeostasis in murine T2D models by enhancing insulin sensitivity and secretion.
	SN-401 improves systemic insulin sensitivity, tissue glucose uptake, and nonalcoholic fatty liver disease in murine T2D models.
	SN-401 inhibits ICl,SWELL but promote SWELL1-dependent signaling at sub-micromolar concentrations (0.1-1 uM).
	SN-401 prevents reductions in SWELL1 protein and rescues SWELL1-dependent islet insulin secretion under glucolipotoxic conditions.
	SN-401 congeners improve glycemic control in murine T2D models
| M.Wt | 427.36 | |
| Formula | C22H28Cl2O4 | |
| Appearance | Solid | |
| Storage | 
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| Solubility | 10 mM in DMSO | |
| Chemical Name/SMILES | 4-((2-Butyl-6,7-dichloro-2-cyclopentyl-1-oxo-2,3-dihydro-1H-inden-5-yl)oxy)butanoic acid | |
1. David M Kern, et al. Elife. 2019 Feb 18;8:e42636.
2. Gunasekar SK, et al. Nat Commun. 2022 Feb 10;13(1):784.

 
                 
                 
                 
                 
                 
                 
                 
                 
            
            
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