Cas no 1332881-65-8 (Taurodeoxycholic-d4 Acid)

Taurodeoxycholic-d4 Acid is a deuterium-labeled analog of taurodeoxycholic acid, a bile acid derivative. The incorporation of four deuterium atoms enhances its utility as an internal standard in mass spectrometry-based analyses, ensuring precise quantification of endogenous bile acids in complex biological matrices. Its high isotopic purity (>98%) and chemical stability make it particularly valuable for metabolic studies, pharmacokinetic research, and investigations into bile acid-related disorders. The deuterium labeling minimizes interference with natural isotopes, improving analytical accuracy. This compound is widely used in lipidomics and hepatobiliary research due to its compatibility with LC-MS/MS methodologies, offering reliable reproducibility in quantitative assays.
Taurodeoxycholic-d4 Acid structure
Taurodeoxycholic-d4 Acid structure
Product Name:Taurodeoxycholic-d4 Acid
CAS No:1332881-65-8
MF:C26H41D4NO6S
MW:503.73
CID:4762879
Update Time:2025-05-20

Taurodeoxycholic-d4 Acid Chemical and Physical Properties

Names and Identifiers

    • Taurodeoxycholic-d4 Acid
    • Taurodeoxycholic Acid-d4 MaxSpec? Standard
    • Inchi: 1S/C26H45NO6S/c1-16(4-9-24(30)27-12-13-34(31,32)33)20-7-8-21-19-6-5-17-14-18(28)10-11-25(17,2)22(19)15-23(29)26(20,21)3/h16-23,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33)/t16-,17-,18-,19+,20-,21+,22+,23+,25+,26-/m1/s1/i10D2,14D2
    • InChI Key: AWDRATDZQPNJFN-QFNLNYLLSA-N
    • SMILES: C[C@]12[C@H](C[C@]3([H])[C@]4(CC([2H])([2H])[C@@H](O)C([2H])([2H])[C@@]4([H])CC[C@@]3([H])[C@]1([H])CC[C@]2([H])[C@H](C)CCC(=O)NCCS(O)(=O)=O)C)O

Taurodeoxycholic-d4 Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on Taurodeoxycholic-d4 Acid

Taurodeoxycholic-d4 Acid (CAS No. 1332881-65-8): An Overview of a Promising Compound in Biomedical Research

Taurodeoxycholic-d4 Acid (CAS No. 1332881-65-8) is a deuterated derivative of taurodeoxycholic acid, a bile acid that plays a crucial role in various physiological processes. This compound has gained significant attention in recent years due to its potential applications in biomedical research, particularly in the fields of drug metabolism, pharmacokinetics, and disease biomarker studies.

The primary function of taurodeoxycholic acid is to facilitate the absorption of fats and fat-soluble vitamins in the intestines. It is synthesized from cholesterol in the liver and conjugated with taurine to form taurodeoxycholic acid. The deuterated form, Taurodeoxycholic-d4 Acid, is structurally identical to its non-deuterated counterpart but contains four deuterium atoms, which can significantly alter its metabolic stability and pharmacokinetic properties.

Recent studies have highlighted the importance of bile acids, including taurodeoxycholic acid, in regulating various metabolic pathways. For instance, bile acids are known to activate nuclear receptors such as farnesoid X receptor (FXR) and G protein-coupled bile acid receptor (TGR5), which are involved in glucose and lipid metabolism. The deuterated form, Taurodeoxycholic-d4 Acid, has been used as a stable isotope tracer to investigate these pathways more accurately.

In the context of drug metabolism, Taurodeoxycholic-d4 Acid serves as an excellent tool for studying the biotransformation of bile acids and their interactions with drug-metabolizing enzymes. Deuterium labeling can provide valuable insights into the metabolic fate of these compounds, helping researchers understand how they are processed by the liver and other organs. This information is crucial for optimizing drug formulations and predicting potential drug-drug interactions.

Beyond its role in metabolism, Taurodeoxycholic-d4 Acid has also shown promise in disease biomarker research. Bile acids are known to be dysregulated in various diseases, including liver diseases, metabolic disorders, and certain types of cancer. By using deuterated bile acids as tracers, researchers can more accurately measure changes in bile acid levels and identify potential biomarkers for early diagnosis and prognosis.

Clinical trials involving Taurodeoxycholic-d4 Acid have demonstrated its utility in assessing the efficacy of therapeutic interventions. For example, in patients with non-alcoholic fatty liver disease (NAFLD), the administration of deuterated bile acids can help monitor changes in bile acid homeostasis and evaluate the effectiveness of treatments aimed at restoring normal metabolic function.

The use of deuterated compounds like Taurodeoxycholic-d4 Acid also has implications for personalized medicine. By providing detailed information on individual metabolic profiles, these tracers can help tailor treatment strategies to specific patient needs, potentially improving outcomes and reducing side effects.

In conclusion, Taurodeoxycholic-d4 Acid (CAS No. 1332881-65-8) is a valuable tool in biomedical research, offering unique insights into bile acid metabolism, drug interactions, and disease biomarkers. Its stable isotope properties make it an ideal tracer for a wide range of applications, from basic research to clinical diagnostics. As our understanding of bile acid biology continues to evolve, the role of compounds like Taurodeoxycholic-d4 Acid will likely become even more significant in advancing medical science.

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