Glycochenodeoxycholic acid

Synonyms: Glycochenodeoxycholate, Chenodeoxycholylglycine, Glycine chenodeoxycholate

Glycochenodeoxycholic acid (Glycochenodeoxycholate, Chenodeoxycholylglycine, Glycine chenodeoxycholate) is a bile salt formed in the liver from chenodeoxycholate and glycine. It acts as a detergent to solubilize fats for absorption. Glycochenodeoxycholic acid

Glycochenodeoxycholic acid Chemical Structure

Glycochenodeoxycholic acid Chemical Structure

CAS: 640-79-9

Selleck's Glycochenodeoxycholic acid has been cited by 1 publication

Purity & Quality Control

Batch: S579401 DMSO] 90 mg/mL] false] Ethanol] 90 mg/mL] false] Water] Insoluble] false Purity: 99.35%
99.35

Glycochenodeoxycholic acid Related Products

Biological Activity

Description Glycochenodeoxycholic acid (Glycochenodeoxycholate, Chenodeoxycholylglycine, Glycine chenodeoxycholate) is a bile salt formed in the liver from chenodeoxycholate and glycine. It acts as a detergent to solubilize fats for absorption. Glycochenodeoxycholic acid
In vitro
In vitro

Glycochenodeoxycholic acid promotes chemoresistance in HCC cells by down-regulating and up-regulating the expression of apoptotic and anti-apoptotic genes, respectively. Furthermore, Glycochenodeoxycholic acid induces the EMT phenotype and stemness in HCC cells and activated the STAT3 signaling pathway. [1]

Cell Research Cell lines hepatocellular carcinoma (HCC) cell lines
Concentrations 200 μM
Incubation Time 24 h
Method

HCC cells are treated with Glycochenodeoxycholic acid and chemotherapeuticdrugs5-fluorouracil (5-FU) (120μg/mL) and cisplatin (10 μg/mL), and the cell viability is detected using the CCK-8 assay.

In Vivo
In vivo

Glycochenodeoxycholic acid exerts effects on hypothalamic CRH expression after their uptake through the apical sodium-dependent bile acid transporter and subsequent activation of the glucocorticoid receptor.

Chemical Information & Solubility

Molecular Weight 449.62 Formula

C26H43NO5

CAS No. 640-79-9 SDF --
Smiles CC(CCC(=O)NCC(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 90 mg/mL ( (200.16 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 90 mg/mL

Water : Insoluble


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In vivo
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Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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