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CaCCinh-A01

Catalog No. T4330   CAS 407587-33-1

CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM).

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CaCCinh-A01 Chemical Structure
CaCCinh-A01, CAS 407587-33-1
Pack Size Availability Price/USD Quantity
5 mg In stock $ 52.00
10 mg In stock $ 84.00
25 mg In stock $ 189.00
50 mg In stock $ 313.00
100 mg In stock $ 528.00
1 mL * 10 mM (in DMSO) In stock $ 57.00
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Purity: 99.92%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM).
Targets&IC50 CaCC:10 μM, TMEM16A:2.1 μM
In vitro Tannic acid (100 μM) and CaCCinh-A01 (30 μM) effectively inhibit CaCC current following ATP stimulation[1]. CaCCinh-A01 (0.1/1/10 μM) reduces Calcium-dependent chloride current (38±14, 66±10, and 91±1%). ATP-induced short-circuits currents are reduced by 38±7 and 78±3% at 10 and 30 μM CaCCinh-A01, respectively.
Cell Research Each well of a 96-well plate is washed three times with PBS (200 μL/wash), leaving 50 μL of PBS. Test compounds (including CaCCinh-A01) (0.5 μL) are added to each well at 25 μM final concentration. After 10 min, 96-well plates are transferred to a plate reader for fluorescence assay. Each well is assayed individually for TMEM16A-mediated I- influx by recording fluorescence continuously (400 ms/point) for 2 s (baseline), then 50 μL of a 140 mM I-solution containing 200 μM ATP is added.
Molecular Weight 347.43
Formula C18H21NO4S
CAS No. 407587-33-1

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 55 mg/mL (158.31 mM)

TargetMolReferences and Literature

1. Namkung W,etal.TMEM16A inhibitors reveal TMEM16A as a minor component of calcium-activated chloridechannel conductance in airway and intestinal epithelial cells. J Biol Chem. 2011 Jan 21;286(3):2365-74. 2. De La Fuente R, et al. Small-molecule screen identifies inhibitors of a human intestinal calcium-activated chloridechannel. Mol Pharmacol. 2008 Mar;73(3):758-68.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Anti-Cancer Compound Library Bioactive Compound Library NO PAINS Compound Library Bioactive Compounds Library Max Immunology/Inflammation Compound Library Ion Channel Inhibitor Library

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Keywords

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