Tauroursodeoxycholate NEW
| Price | $50 | $63 |
| Package | 50mg | 100mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2026-03-26 |
Product Details
| Product Name: Tauroursodeoxycholate | CAS No.: 14605-22-2 |
| Purity: 98.77% | Supply Ability: 10g |
| Release date: 2026/03/26 |
Product Introduction
Bioactivity
| Name | Tauroursodeoxycholate |
| Description | Tauroursodeoxycholate (UR 906), also known as ursodoxicoltaurine, is a highly hydrophilic tertiary bile acid that is produced in humans at a low concentration. Tauroursodeoxycholate is the more hydrophilic form of ursodeoxycholic acid, which is the more abundant naturally produced bile acid in humans.Tauroursodeoxycholate is being investigated for use in several conditions such as Primary Biliary Cirrhosis (PBC), insulin resistance, amyloidosis, Cystic Fibrosis, Cholestasis, and Amyotrophic Lateral Sclerosis. |
| In vitro | METHODS: HeLa cells overexpressing the WDR45 mutation were treated with Tauroursodeoxycholate (200 µM) for 24 h, and the expression levels of target proteins were measured by Western Blot. RESULTS: Inhibition of ER stress with Tauroursodeoxycholate significantly reduced the phosphorylation of p38 and LAMP2A as well as the punctate formation of mCherry KFERQ in cells expressing mutant WDR45. [1] METHODS: Undifferentiated neural stem cells NSCs were treated with Tauroursodeoxycholate (100 µM) for 24 h and cell proliferation was detected by Flow cytometry via BrdU. RESULTS: BrdU incorporation increased significantly after incubation with Tauroursodeoxycholate, and Tauroursodeoxycholate regulated cell proliferation. Tauroursodeoxycholate regulates cell proliferation.[2] |
| In vivo | METHODS: To test the effect on diabetes, Tauroursodeoxycholate (300 mg/kg) was administered intraperitoneally to STZ-induced diabetic C57BL/6 mice once daily for 24 days. RESULTS: After 15 days of treatment, STZ+Tauroursodeoxycholate mice had a 43% reduction in blood glucose compared to the STZ group. This decrease may be due to an increase in insulinemia. [3] |
| Storage | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | H2O : 100 mg/mL (200.12 mM), Sonication is recommended. 5% DMSO+95% Saline : 4.5 mg/mL (9.01 mM), Solution. DMSO : 6.25 mg/mL (12.51 mM), Sonication is recommended. |
| Keywords | UR-906 | UR906 | Tauroursodeoxycholate | stress | reticulum | molecules | Inhibitor | inhibit | Extracellular signal regulated kinases | ERK | endoplasmic | EndogenousMetabolite | Endogenous Metabolite | CYP3A | caspase-3 | caspase-12 | Caspase | Apoptosis |
| Inhibitors Related | Sucrose | Aceglutamide | L-Pyroglutamic acid | Nicotinamide riboside malate | D(+)-Raffinose pentahydrate | Guanidine hydrochloride | Formamide | Glycerol | Thymidine | Corn starch | Hyaluronic acid sodium (MW 20 kDa) | Gluconate Calcium |
| Related Compound Libraries | Anti-Tumor Natural Product Library | Bioactive Compound Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | Anti-Inflammatory Traditional Chinese Medicine Compound Library | Inhibitor Library | Anti-Cancer Approved Drug Library | Natural Product Library for HTS | FDA-Approved Kinase Inhibitor Library | Human Endogenous Metabolite Library | Anti-Aging Compound Library | Anti-Cancer Drug Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
Citations
[1] Zhou, J., Shi, Y., Zhao, L., Wang, R., Luo, L., & Yin, Z. (2025). γ-Glutamylcysteine restores glucolipotoxicity-induced islet β-cell apoptosis and dysfunction via inhibiting endoplasmic reticulum stress. Toxicology and Applied Pharmacology, 495, Article 117206. https://doi.org/10.1016/j.taap.2024.117206
[2] Xiong, Q., Sun, H., Xing, W., Li, X., Chen, G., Zhao, Z., Wu, C., & Li, P. (2023). WDR45 mutation dysregulates iron homeostasis by promoting the chaperone-mediated autophagic degradation of ferritin heavy chain in an ER stress/p38 dependent mechanism. Free Radical Biology and Medicine, 201, Pages 89-97. https://doi.org/10.1016/j.freeradbiomed.2023.03.012
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- Since: 2011-01-07
- Address: 36 Washington Street, Wellesley Hill, MA
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