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Tauroursodeoxycholate (sodium)

CAT: 0804-HY-19696A-02Size: 10 mM - 1 mLDry Ice: NoHazardous: No
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CAT#:0804-HY-19696A-02Size:10 mM - 1 mL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Tauroursodeoxycholate (Tauroursodeoxycholic acid; TUDCA) sodium is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK.
CAS Number
35807-85-3
Product Name Alternative
Tauroursodeoxycholic acid (sodium) ; TUDCA (sodium) ; UR 906 (sodium)
UNSPSC
12352211
Hazard Statement
H302, H315, H319, H335
Target
Apoptosis; Caspase; Endogenous Metabolite; ERK
Type
Reference compound
Related Pathways
Apoptosis; MAPK/ERK Pathway; Metabolic Enzyme/Protease; Stem Cell/Wnt
Applications
Cancer-Kinase/protease
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/Tauroursodeoxycholate-Sodium.html
Concentration
10mM
Purity
98.40
Solubility
DMSO : 100 mg/mL (ultrasonic) |H2O : 100 mg/mL (ultrasonic)
Smiles
C[C@H](CCC(NCCS(=O)(O[Na])=O)=O)[C@H]1CC[C@@]2([H])[C@]3([H])[C@@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C
Molecular Formula
C26H44NNaO6S
Molecular Weight
521.69
Precautions
H302, H315, H319, H335
References & Citations
[1]Kim SY, et al. Tauroursodeoxycholate (TUDCA) inhibits neointimal hyperplasia by suppression of ERK via PKCα-mediated MKP-1 induction. Cardiovasc Res. 2011 Nov 1;92 (2) :307-16.|[2]Qin Y, et al. Tauroursodeoxycholic Acid Attenuates Angiotensin II Induced Abdominal Aortic Aneurysm Formation in Apolipoprotein E-deficient Mice by Inhibiting Endoplasmic Reticulum Stress. Eur J Vasc Endovasc Surg. 2017 Mar;53 (3) :337-345.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
Caspase 12; Caspase 3; ERK; Human Endogenous Metabolite
Citation 01
Arch Toxicol. 2025 Aug 20.|Biochem Pharmacol. 2018 Aug:154:278-292.|Biofabrication. 2021 May 5;13 (3) .|bioRxiv. 2020 Jun.|Brain Res Bull. 2020 Sep;162:73-83.|Cell Biol Toxicol. 2024 Jan 22;40 (1) :1.|Cell Prolif. 2021 Nov;54 (11) :e13133.|Cell Stress Chaperones. 2022 May;27 (3) :273-283.|Ecotoxicol Environ Saf. 2022 May 1;236:113508.|FASEB J. 2025 Jun 15;39 (11) :e70695.|FEBS Open Bio. 2020 Oct;10 (10) :2122-2136.|Fundam Clin Pharmacol. 2018 Aug;32 (4) :363-377.|Int J Mol Sci. 2023 Jul 20;24 (14) :11692.|Mater Design. 8 November 2021, 110229.|MedComm-Oncology. 2023 Feb 19.|Mol Ther. 2023 Mar 1;31 (3) :890-908.|Nat Cell Biol. 2023 May;25 (5) :726-739.|Nutrients. 2021 Dec 1;13 (12) :4343.|Oxid Med Cell Longev. 2022 Aug 31;2022:9004738.|Research Square Preprint. 2023 Oct 16.|Sci Rep. 2017 Aug 30;7 (1) :9967. |Virol J. 2025 Nov 17;22 (1) :378.|Adv Sci (Weinh) . 2021 Nov;8 (21) :e2101936.|Adv Sci (Weinh) . 2025 Feb 3:e2411719.|Am J Pathol. 2024 Jan;194 (1) :85-100.|Anim Cells Syst. 2023 Nov 27.|Appl Biochem Biotechnol. 2024 Oct;196 (10) :7362-7374.|Biochem Biophys Res Commun. 2021 Mar 12:544:44-51.|Biochem Biophys Res Commun. 2024 Apr 25:149972.|Biochem Biophys Res Commun. 2024 May 14:708:149770.|Biochem Pharmacol. 2025 Dec;242 (Pt 4) :117377.|Biochem Pharmacol. 2025 Jun:236:116868.|Biomed Pharmacother. 2019 Dec;120:109475.|Biomed Pharmacother. 2022 May 24;151:113173.|Biomed Pharmacother. 2023 Aug:164:114897.|BMC Mol Cell Biol. 2023 Mar 3;24 (1) :7.|Br J Pharmacol. 2019 Jul;176 (13) :2162-2178. |Cancer Med. 2023 Jun;12 (12) :13610-13622.|Cancers. 2020 Mar 6;12 (3) :613.|Cell Biol Toxicol. 2023 Jun;39 (3) :907-928.|Cell Biol Toxicol. 2025 Mar 7;41 (1) :56.|Cell Death Dis. 2020 Apr 24;11 (4) :279.|Cell Death Dis. 2023 Aug 15;14 (8) :524.|Cell Host Microbe. 2025 Aug 19:S1931-3128 (25) 00291-4.|Cell Rep. 2023 Dec 27;43 (1) :113591.|Cell Rep. 2025 Nov 25;44 (11) :116502.|Cell Signal. 2024 Dec 8:127:111560.|Chem Res Toxicol. 2025 Feb 17;38 (2) :314-324.|Chin Med J (Engl) . 2025 Jan 5;138 (1) :79-92.|Cytokine. 2020 Mar;127:154959.|Cytokine. 2026 Jan:197:157068.|Departamento de Biotecnología. 2020 Sep.|Diagn Microbiol Infect Dis. 2024 Aug 22;110 (4) :116500.|Ecotoxicol Environ Saf. 2024 Jan 15:270:115895.|Environ Pollut. 2025 Oct 6:127217.|FASEB J. 2025 Jun 15;39 (11) :e70715.|Food Chem Toxicol. 2018 Oct:120:253-260.|Food Chem Toxicol. 2025 Jun 4:203:115592.|Front Cell Dev Biol. 2020 May 12;8:269.|Front Pharmacol. 2021 Aug 23;12:708462.|Front Pharmacol. 2022 Sep 16;13:977622.|Gut Microbes. 2024 Jan-Dec;16 (1) :2392877.|Infect Genet Evol. 2020 Nov;85:104552.|Int Heart J. 2023 Mar 31;64 (2) :283-293.|Int Immunopharmacol. 2021 Jun:95:107519.|Int Immunopharmacol. 2025 Jan 3:147:113982.|Int Immunopharmacol. 2025 Sep 6:165:115471.|J Agric Food Chem. 2025 Aug 13;73 (32) :20235-20253.|J Agric Food Chem. 2025 Aug 6;73 (31) :19442-19459.|J Cachexia Sarcopenia Muscle. 2021 Dec;12 (6) :1553-1569.|J Cell Mol Med. 2019 Oct;23 (10) :7029-7042.|J Inflamm. 2023 Nov 1;20 (1) :36.|J Int Med Res. 2023 May;51 (5) :3000605231173272.|J Pharm Anal. 2024 Aug 22.|J Pharm Biomed Anal. 2025 Jul 15:259:116760.|J Steroid Biochem Mol Biol. 2024 Aug 13:106599.|J Trace Elem Med Biol. 2024 Aug 28:86:127512.|Life Sci. 2025 May 15:369:123526.|Nat Commun. 2025 Aug 16;16 (1) :7638.|Nature. 2025 Jul;643 (8070) :192-200.|Nutr Diabetes. 2024 Sep 13;14 (1) :75.|Nutr Metab. 2020 Jan 30;17:11.|Pharmacology. 2018 Dec 5;103 (1-2) :93-100. |Phytomedicine.2023 Sep:118:154971.|PLoS One. 2023 May 18;18 (5) :e0283943.|Redox Biol. 2023 Oct:66:102861.|Research Square Preprint. 2023 Oct 23.|Respir Res. 2025 Apr 12;26 (1) :136.|Sci Total Environ. 2024 Jul 6:174536.|Sci Total Environ. 2024 Jun 25:946:174299.

Chemical Information

Taurursodiol sodium
CAS Number35807-85-3
PubChem CID46782978
IUPAC Namesodium 2-[[(4R)-4-[(3R,5S,7S,8R,9S,10S,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonate
Molecular FormulaC26H44NNaO6S
Molecular Weight521.7
Topological Polar Surface Area135
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Heavy Atom Count35
Formal Charge0
Complexity864
SMILES
C[C@H](CCC(=O)NCCS(=O)(=O)[O-])[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2[C@H](C[C@H]4[C@@]3(CC[C@H](C4)O)C)O)C.[Na+]
InChI
InChI=1S/C26H45NO6S.Na/c1-16(4-7-23(30)27-12-13-34(31,32)33)19-5-6-20-24-21(9-11-26(19,20)3)25(2)10-8-18(28)14-17(25)15-22(24)29;/h16-22,24,28-29H,4-15H2,1-3H3,(H,27,30)(H,31,32,33);/q;+1/p-1/t16-,17+,18-,19-,20+,21+,22+,24+,25+,26-;/m1./s1
InChIKey
IYPNVUSIMGAJFC-JUWYWQLMSA-M
Chemical Structure
2D Structure
2D structure of Taurursodiol sodium
CAS: 35807-85-3
CID: 46782978
Formula: C26H44NNaO6S
MW: 521.7
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight521.7
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass521.27870358
Monoisotopic Mass521.27870358
Topological Polar Surface Area135 Ų
Heavy Atom Count35
Formal Charge0
Complexity864
Isotope Atom Count0
Defined Atom Stereocenter Count10
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes