Name | 4-[(2-butyl-6,7-dichloro-2-cyclopentyl-1-oxo-3H-inden-5-yl)oxy]butanoic acid |
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Synonyms |
dcpib
hms3268c07 |
Description | DCPIB is a selective, reversible and potent inhibitor of volume-regulated anion channels (VRAC), voltage-dependently activates potassium channels TREK1 and TRAAK, inhibits TRESK, TASK1 and TASK3 (IC50s, 0.14, 0.95, 50.72 μM, respectively)[1]. DCPIB is also a selective blocker of swelling-induced chloride current (ICl,swell), with an IC50 of 4.1 μM in CPAE cells[2]. |
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Related Catalog | |
Target |
IC50:0.14 μM (TRESK), 0.95 μM (TASK1), 50.72 μM (TASK3)[1], 4.1 μM (ICl,swell, CPAE cells)[2] |
References |
Density | 1.263g/cm3 |
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Boiling Point | 593.835ºC at 760 mmHg |
Molecular Formula | C22H28Cl2O4 |
Molecular Weight | 427.36 |
Flash Point | 312.94ºC |
Exact Mass | 426.13600 |
PSA | 63.60000 |
LogP | 6.34260 |
Index of Refraction | 1.564 |
Storage condition | 2-8℃ |
Precursor 4 | |
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DownStream 0 |