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Chenodeoxycholic acid

SKU: orb1310239

Description

Chenodeoxycholic acid

Research Area

Cell Biology, Metabolism Research, Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number474-25-9
MW392.57
Purity99.97% (May vary between batches)
FormulaC24H40O4
SMILES[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)CC2C[C@H](O)CC[C@]12C
TargetEndogenous Metabolite|||Potassium Channel|||FXR|||Autophagy
SolubilityH2O:< 1 mg/mL (insoluble or slightly soluble);DMSO:40 mg/mL (101.89 mM);Ethanol:79 mg/mL (201.24 mM)

Bioactivity

Target IC50
A549 cells:> 200 mM|Caco-2 cells:106 μM|CHO cells:15.6 μM
In Vitro
METHODS: Caco-2 cells were treated with Chenodeoxycholic acid (0.1-1000 μM) for 24 hours, and cell growth inhibition was measured by MTT assay. RESULTS: Chenodeoxycholic acid significantly inhibited Caco-2 cell growth (IC50=106 μM).
Cell Research
The cell viability is analyzed by incubating transfected HEK-293 cells and CHO cells for 1 h with the corresponding concentration of bile acid and staining with trypan blue. The toxicity of bile acids is analyzed using the tetrazolium salt MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) according to the cell proliferation kit I. No significant differences between control and bile acid-treated cells are obtained in both tests.

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

PotassiumChannel, Potassium Channel, Inhibitor, Endogenous Metabolite, EndogenousMetabolite, FXR, inhibit, NR1H4, CDCA, Chenodeoxycholic acid, Chenodiol, Bile acid receptor, Autophagy

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Key Properties

No computed properties available.

Protocol Information

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1 ml x 10 mM (in DMSO)
$ 90.00
100 mg
$ 100.00
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