CAS 35807-85-3
:tauroursodeoxycholic acid sodium salt
Description:
Tauroursodeoxycholic acid sodium salt, commonly referred to as TUDCA, is a bile acid derivative that plays a significant role in various biological processes. It is a water-soluble compound, which enhances its bioavailability and facilitates its use in therapeutic applications. TUDCA is known for its cytoprotective properties, particularly in protecting cells from apoptosis and promoting cell survival under stress conditions. It has been studied for its potential benefits in liver diseases, neurodegenerative disorders, and metabolic syndromes. The sodium salt form enhances its solubility and stability, making it suitable for pharmaceutical formulations. TUDCA also exhibits antioxidant properties and may help in the regulation of bile flow and cholesterol metabolism. Its mechanism of action involves modulation of cellular signaling pathways, contributing to its protective effects. Overall, TUDCA is a compound of interest in both clinical and research settings due to its diverse biological activities and therapeutic potential.
Formula:C26H44NNaO6S
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Found 10 products.
Tauroursodeoxycholic acid sodium salt
CAS:Formula:C26H44NNaO6SPurity:97%Color and Shape:SolidMolecular weight:521.6854Tauroursodeoxycholate Sodium
CAS:<p>Tauroursodeoxycholate Sodium</p>Formula:C26H44NO6S·NaPurity:98.0% (Typical Value in Batch COA)Color and Shape: off-white solidMolecular weight:521.69g/molTauroursodeoxycholate sodium
CAS:<p>Tauroursodeoxycholate sodium (TUDC) is an endoplasmic reticulum (ER) stress inhibitor, used for the treatment of gallstones and liver cirrhosis.</p>Formula:C26H44NNaO6SPurity:97.90%Color and Shape:SolidMolecular weight:521.69Tauroursodeoxycholic Acid Sodium Salt (90%)
CAS:<p>Applications Tauroursodeoxycholate inhibits human cholangiocarcinoma growth via Ca2+-, PKC-, and MAPK-dependent pathways.<br>References Alvarez, E., et al.: J. Biol. Chem., 266, 15277 (1991), Alvaro, D., et al.: J. Clin. Invest., 96, 665 (1995), Alpini, G., et al.: Hepatology, 34, 868 (2001), Higuchi, H., et al.: J. Biol. Chem., 278, 454 (2003)<br></p>Formula:C26H44NO6S·NaPurity:90%Color and Shape:Off White To Light BeigeMolecular weight:521.69Sodium Tauroursodeoxycholate (TUDCA Sodium) extrapure, 98%
CAS:Formula:C26H44NO6SNaPurity:min. 98%Color and Shape:White to off- white, Crystalline powderMolecular weight:521.69Tauroursodeoxycholic Acid Sodium Salt
CAS:<p>Applications Tauroursodeoxycholic Acid Sodium Salt is a bile related salt for isolation of lipids and membrane-bound proteins. It is a sodium salt form of Tauroursodeoxycholic Acid which can be used in biological study of inhibition of alpha-naphthyl isothiocyanate-induced liver injury and bile acid cycle disruption by glycyrrhizin and glycyrrhetinic acid.<br>References Tsuchimoto, D., et al.: J. Gastroenterol. Hepatol., 14, 388 (1999); Wang, H., et al.: Toxicology, (2017)<br></p>Formula:C26H44NO6S·NaColor and Shape:NeatMolecular weight:521.69Tauroursodeoxycholic acid sodium (90%)
CAS:<p>Tauroursodeoxycholic acid sodium salt (90%) is a bile acid derivative, which is synthesized from ursodeoxycholic acid and taurine. This compound acts as a chemical chaperone, facilitating protein folding and mitigating endoplasmic reticulum stress. It stabilizes hydrophobic interactions and enhances protein solubility, thereby contributing to cellular homeostasis.</p>Formula:C26H45NO6S•NaPurity:Min. 95%Molecular weight:522.7 g/molTauroursodeoxycholic acid, sodium salt
CAS:<p>Tauroursodeoxycholic acid, sodium salt is a taurine-conjugated bile acid derivative, which is synthesized in the liver from ursodeoxycholic acid. It functions through its role in stabilizing the mitochondria and inhibiting apoptosis by modulating the unfolded protein response. This molecular action involves reducing endoplasmic reticulum stress, thereby providing cytoprotective effects in various cellular environments.</p>Formula:C26H44NNaO6SPurity:Min. 95%Molecular weight:521.69 g/mol
