Identification
- Summary
-
Tauroursodeoxycholic acidis the taurine conjugate of ursodeoxycholic acid with antiapoptotic and ER stress response dampening effects used in some countries to treat gallstones. It is also being investigated for a wide variety of other conditions.
- Brand Names
-
Relyvrio
- Generic Name
- Tauroursodeoxycholic acid
- DrugBank Accession Number
- DB08834
- Background
-
Tauroursodeoxycholic acid, also known as ursodoxicoltaurine, is a highly hydrophilic tertiary bile acid3that is produced in humans at a low concentration.3It is a taurine conjugate ofursodeoxycholic acid2with comparable therapeutic efficacy and safety,3but a much higher hydrophilicity.1Normally, hydrophilic bile acids regulates hydrophobic bile acids and their cytotoxic effects. Tauroursodeoxycholic acid can reduce the absorption of cholesterol in the small intestine, thereby reducing the body's intake of dietary cholesterol and the body cholesterol content.4
Tauroursodeoxycholic acid is currently used in Europe to treat and prevent gallstones as a bile acid derivative.7Due to a range of its molecular properties - namely its anti-apoptotic effects - tauroursodeoxycholic acid has been examined in inflammatory metabolic diseases and neurodegenerative diseases.2,3
- Type
- Small Molecule
- Groups
- Approved, Investigational
- Structure
-
Structure for Tauroursodeoxycholic acid (DB08834)
- Weight
-
Average: 499.71
Monoisotopic: 499.296759347 - Chemical Formula
- C26H45NO6S
- Synonyms
-
- Tauroursodeoxycholate
- Tauroursodesoxycholic acid
- Taurursodiol
- TUDCA
- Ursodeoxycholyltaurine
- Ursodoxicoltaurine
- External IDs
-
- UR-906
Pharmacology
- Indication
-
Tauroursodeoxycholic acid is used to prevent and treat gallstone formation.7
Tauroursodeoxycholic acid is used in combination withphenylbutyric acidto treat amyotrophic lateral sclerosis (ALS) in adults.8,9
Reduce drug development failure ratesBuild, train, & validate machine-learning models
with evidence-based and structured datasets.Build, train, & validate predictive machine-learning models with structured datasets. - Associated Conditions
- Contraindications & Blackbox Warnings
-
Avoid life-threatening adverse drug eventsImprove clinical decision support with information oncontraindications & blackbox warnings, population restrictions, harmful risks, & more.Avoid life-threatening adverse drug events & improve clinical decision support. - Pharmacodynamics
-
Tauroursodeoxycholic acid works to decrease bile acid1and cholesterol levels.4It reduces the cholesterol content and increases the bile acid content in gallbladder bile to prevent the formation of cholesterol gallstones.4
Tauroursodeoxycholic acid possesses anti-apoptotic and anti-inflammatory properties. These findings provoked the investigations of tauroursodeoxycholic acid as a potential therapeutic agent for neurodegenerative diseases, such as amyotrophic lateral sclerosis, Alzheimer's disease, and Parkinson's disease.2Other studies also suggest that tauroursodeoxycholic acid can promote angiogenesis and suppress adipogenesis of adipose-derived mesenchymal stem cells (MSCs). Anti-osteoporotic effects of tauroursodeoxycholic acid have also been documented, as it was shown to enhance osteogenic differentiation of bone marrow-derived MSCs.3
- Mechanism of action
-
About 90% of gallstones are formed by cholesterol, which may be caused by altered gut microbiota from a high-fat diet and other factors. The gut microbiota regulates bile acid metabolism; thus, altered composition in gut microbiota may significantly change the bile acid pool and alter cholesterol secretion.4
While the exact mechanism of action of tauroursodeoxycholic acid in reducing and preventing gallstone formation is unclear, tauroursodeoxycholic acid may achieve this effect in a number of ways. A recent mouse study suggests that tauroursodeoxycholic acid inhibits intestinal cholesterol absorption and lowers liver cholesterol levels by upregulating the bile acid excretion from the liver to the gallbladder. Tauroursodeoxycholic acid lowers the bile cholesterol saturation in the gallbladder, thereby increasing the solubility of cholesterol in bile. It can also maintain a specific gut microbiota composition to promote the synthesis of bile acids and reduce liver inflammation caused by the lipopolysaccharide in the blood. Ultimately, tauroursodeoxycholic acid enhances the synthesis of bile acids in the liver and reduces cholesterol in the serum and liver.4
Tauroursodeoxycholic acid inhibits cell apoptosis by disrupting the mitochondrial pathway of cell death. It works by inhibiting oxygen-radical production, ameliorating endoplasmic reticulum (ER) stress, and stabilizing the unfolded protein response. Other anti-apoptotic processes mediated by tauroursodeoxycholic acid include cytochrome c release, caspase activation, DNA and nuclear fragmentation, and inhibition of p53 transactivation. It is believed that tauroursodeoxycholic acid works on multiple cellular targets to inhibit apoptosis and upregulate survival pathways.2
Target 行动 Organism UIntegrin alpha-5 activatorHumans - Absorption
-
Not Available
- d的体积istribution
-
There is evidence that tauroursodeoxycholic acid crosses the blood brain barrier in humans.2
- Protein binding
-
Not Available
- Metabolism
-
几乎没有tauroursodeox的生物转化ycholic acid. It is partially deconjugated by intestinal microflora to form unconjugated bile acids.5,6
- Route of elimination
-
Not Available
- Half-life
-
Not Available
- Clearance
-
Not Available
- 的不利影响
-
Improve decision support & research outcomesWith structured adverse effects data, including:blackbox warnings, adverse reactions, warning & precautions, & incidence rates.Improve decision support & research outcomes with our structured adverse effects data. - Toxicity
-
There is no information available regarding the LD50and overdose of tauroursodeoxycholic acid.
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRsBrowse all" title="" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
- Not Available
Interactions
- Drug InteractionsLearn More" title="" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
-
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAbciximab The risk or severity of adverse effects can be increased when Abciximab is combined with Tauroursodeoxycholic acid. Acenocoumarol The risk or severity of bleeding and bruising can be increased when Acenocoumarol is combined with Tauroursodeoxycholic acid. Acetylsalicylic acid The risk or severity of adverse effects can be increased when Acetylsalicylic acid is combined with Tauroursodeoxycholic acid. Alteplase The risk or severity of bleeding and bruising can be increased when Alteplase is combined with Tauroursodeoxycholic acid. Aluminium phosphate Aluminium phosphate can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. Aluminum chloride Aluminum chloride can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. Aluminum chlorohydrate Aluminum chlorohydrate can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. Aluminum hydroxide Aluminum hydroxide can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. Aluminum oxide Aluminum oxide can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. Aluminum sulfate Aluminum sulfate can cause a decrease in the absorption of Tauroursodeoxycholic acid resulting in a reduced serum concentration and potentially a decrease in efficacy. 
Identify potential medication risksEasily compare up to 40 drugs with our drug interaction checker.Get severity rating, description, and management advice.Learn more - Food Interactions
- No interactions found.
Products
-
Drug product information from 10+ global regionsOur datasets provide approved product information including:
dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions. - Product Ingredients
-
Ingredient UNII CAS InChI Key Tauroursodeoxycholic acid dihydrate U7XRV7RZ1I 117609-50-4 BNXLUNVCHFIPFY-GUBAPICVSA-N - International/Other Brands
- Tauro (Teofarma)/Taurolite (Bio-Gen)
- Mixture Products
-
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image Albrioza Tauroursodeoxycholic acid(1克/袋)+Sodium phenylbutyrate(3 g / sachet) Powder, for suspension Oral Amylyx Pharmaceuticals Inc. 2022-07-29 Not applicable Canada 
Relyvrio Tauroursodeoxycholic acid(1 g/1)+Sodium phenylbutyrate(3 g/1) Powder, for suspension Oral Amylyx Pharmaceuticals Inc 2022-09-29 Not applicable US 
- Unapproved/Other Products
-
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image TAUROLITE 250 MG 100 KAPSUL Tauroursodeoxycholic acid(250 mg) Capsule Oral BİO-GEN İLAÇ SAN.TİC.LTD.ŞTİ. 2020-08-14 Not applicable Turkey 
Categories
- Drug Categories
- Chemical TaxonomyProvided byClassyfire
-
- Description
- This compound belongs to the class of organic compounds known as taurinated bile acids and derivatives. These are bile acid derivatives containing a taurine conjugated to the bile acid moiety.
- Kingdom
- Organic compounds
- Super Class
- Lipids and lipid-like molecules
- Class
- Steroids and steroid derivatives
- Sub Class
- Bile acids, alcohols and derivatives
- Direct Parent
- Taurinated bile acids and derivatives
- Alternative Parents
- Dihydroxy bile acids, alcohols and derivatives/7-alpha-hydroxysteroids/3-alpha-hydroxysteroids/N-acyl amines/Sulfonyls/Organosulfonic acids/Alkanesulfonic acids/Secondary carboxylic acid amides/二级醇/Cyclic alcohols and derivatives show 5 more
- Substituents
- 3-alpha-hydroxysteroid/3-hydroxysteroid/7-alpha-hydroxysteroid/7-hydroxysteroid/Alcohol/Aliphatic homopolycyclic compound/Alkanesulfonic acid/Carbonyl group/Carboxamide group/Carboxylic acid derivative show 22 more
- Molecular Framework
- Aliphatic homopolycyclic compounds
- External Descriptors
- bile acid taurine conjugate (CHEBI:80774)/Taurine conjugates (LMST05040015)
- Affected organisms
-
- Humans and other mammals
Chemical Identifiers
- UNII
- 60EUX8MN5X
- CAS number
- 14605-22-2
- InChI Key
- BHTRKEVKTKCXOH-LBSADWJPSA-N
- InChI
-
InChI=1S/C26H45NO6S/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)/t16-,17+,18-,19-,20+,21+,22+,24+,25+,26-/m1/s1
- IUPAC Name
-
2-[(4R)-4-[(1S,2S,5R,7S,9S,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanamido]ethane-1-sulfonic acid
- SMILES
-
[H][C@@]12CC[C@H]([C@H](C)CCC(=O)NCCS(O)(=O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@@H](O)C[C@]2([H])C[C@H](O)CC[C@]12C
References
- Synthesis Reference
-
Zhuo, Chao; Feng, Wei; Wu, Da-jun; Xiong, Zhi-gang. Synthesis of tauroursodeoxycholic acid. Hecheng Huaxue (2002), 10(5), 444-446.
- General References
-
- Crosignani A, Battezzati PM, Setchell KD, Invernizzi P, Covini G, Zuin M, Podda M: Tauroursodeoxycholic acid for treatment of primary biliary cirrhosis. A dose-response study. Dig Dis Sci. 1996 Apr;41(4):809-15. doi: 10.1007/BF02213140. [Article]
- Vang S, Longley K, Steer CJ, Low WC: The Unexpected Uses of Urso- and Tauroursodeoxycholic Acid in the Treatment of Non-liver Diseases. Glob Adv Health Med. 2014 May;3(3):58-69. doi: 10.7453/gahmj.2014.017. [Article]
- Ahn TK, Kim KT, Joshi HP, Park KH, Kyung JW, Choi UY, Sohn S, Sheen SH, Shin DE, Lee SH, Han IB: Therapeutic Potential of Tauroursodeoxycholic Acid for the Treatment of Osteoporosis. Int J Mol Sci. 2020 Jun 16;21(12). pii: ijms21124274. doi: 10.3390/ijms21124274. [Article]
- Lu Q, Jiang Z, Wang Q, Hu H, Zhao G: The effect of Tauroursodeoxycholic acid (TUDCA) and gut microbiota on murine gallbladder stone formation. Ann Hepatol. 2021 Jul-Aug;23:100289. doi: 10.1016/j.aohep.2020.100289. Epub 2020 Nov 18. [Article]
- Setchell KD, Rodrigues CM, Podda M, Crosignani A: Metabolism of orally administered tauroursodeoxycholic acid in patients with primary biliary cirrhosis. Gut. 1996 Mar;38(3):439-46. doi: 10.1136/gut.38.3.439. [Article]
- Invernizzi P, Setchell KD, Crosignani A, Battezzati PM, Larghi A, O'Connell NC, Podda M: Differences in the metabolism and disposition of ursodeoxycholic acid and of its taurine-conjugated species in patients with primary biliary cirrhosis. Hepatology. 1999 Feb;29(2):320-7. doi: 10.1002/hep.510290220. [Article]
- AIFA: Tauro (Tauroursodeoxycholic Acid) Oral Capsules [Link]
- Health Canada Approved Drug Products: ALBRIOZA (sodium phenylbutyrate and ursodoxicoltaurine) Oral Powder for suspension [Link]
- FDA Approved Drug Products: RELYVRIO (sodium phenylbutyrate and taurursodiol) for oral suspension [Link]
- External Links
-
- KEGG Compound
- C16868
- PubChem Compound
- 9848818
- PubChem Substance
- 175427112
- ChemSpider
- 8024531
- BindingDB
- 50236230
- 2613950
- ChEBI
- 80774
- ChEMBL
- CHEMBL272427
- ZINC
- ZINC000003914813
- PDBe Ligand
- 5D5
- Drugs.com
- Drugs.com Drug Page
- Wikipedia
- Ursodoxicoltaurine
- PDB Entries
- 5dlv/5dlw
Clinical Trials
- Clinical TrialsLearn More" title="" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
-
Phase Status Purpose Conditions Count 4 Unknown Status Prevention Gallstones 1 3 Active Not Recruiting Treatment Amyotrophic Lateral Sclerosis (ALS) 1 3 Active Not Recruiting Treatment TTR Cardiac Amyloidosis 1 3 Completed Treatment Cholestatic Liver Disease 1 3 Completed Treatment Primary Biliary Cholangitis 1 3 Enrolling by Invitation Treatment Amyotrophic Lateral Sclerosis (ALS) 1 2 Completed Treatment Alzheimer's Disease (AD) 1 2 Completed Treatment Amyotrophic Lateral Sclerosis (ALS) 1 2 Completed Treatment Amyotrophic Lateral Sclerosis (ALS)/Central Nervous System Disorder/Diseases of the Nervous System/MND (Motor Neurone Disease)/Neurodegenerative Disorders/Neuromuscular Disorders/Spinal Cord Diseases/TDP-43 Proteinopathies 1 2 Completed Treatment Transthyretin Amyloidosis 1
Pharmacoeconomics
- Manufacturers
-
Not Available
- Packagers
-
Not Available
- Dosage Forms
-
Form Route Strength Powder, for suspension Oral Capsule Oral 150 MG Capsule Oral 250 MG Capsule, delayed release Oral 500 MG Tablet, extended release Oral 500 MG - Prices
- Not Available
- Patents
-
Patent Number Pediatric Extension Approved Expires (estimated) Region US10857162 No 2020-12-08 2033-12-24 US US10251896 No 2019-04-09 2033-12-24 US US9872865 No 2018-01-23 2033-12-24 US US11071742 No 2021-07-27 2033-12-24 US US11583542 No 2020-07-27 2040-07-27 US
Properties
- State
- Solid
- Experimental Properties
- Not Available
- Predicted Properties
-
Property Value Source 水溶度 0.00748 mg/mL ALOGPS logP 1.38 ALOGPS logP 1.1 Chemaxon logS -4.8 ALOGPS pKa (Strongest Acidic) -0.8 Chemaxon pKa最强(基本) -0.32 Chemaxon Physiological Charge -1 Chemaxon Hydrogen Acceptor Count 6 Chemaxon Hydrogen Donor Count 4 Chemaxon Polar Surface Area 123.93 Å2 Chemaxon Rotatable Bond Count 7 Chemaxon Refractivity 130.68 m3·mol-1 Chemaxon Polarizability 56.75 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon - Predicted ADMET Features
-
Property Value Probability Human Intestinal Absorption + 0.9774 Blood Brain Barrier + 0.8416 Caco-2 permeable - 0.8957 P-glycoprotein substrate Non-substrate 0.5136 P-glycoprotein inhibitor I Non-inhibitor 0.6229 P-glycoprotein inhibitor II Non-inhibitor 0.7598 Renal organic cation transporter Non-inhibitor 0.8476 CYP450 2C9 substrate Non-substrate 0.7519 CYP450 2D6 substrate Non-substrate 0.7972 CYP450 3A4 substrate Substrate 0.654 CYP450 1A2 substrate Non-inhibitor 0.7814 CYP450 2C9 inhibitor Non-inhibitor 0.8625 CYP450 2D6 inhibitor Non-inhibitor 0.8685 CYP450 2C19 inhibitor Non-inhibitor 0.8426 CYP450 3A4 inhibitor Non-inhibitor 0.8612 CYP450 inhibitory promiscuity Low CYP Inhibitory Promiscuity 0.7175 Ames test Non AMES toxic 0.6103 Carcinogenicity Non-carcinogens 0.5359 Biodegradation Not ready biodegradable 0.972 Rat acute toxicity 2.0310 LD50, mol/kg Not applicable hERG inhibition (predictor I) Weak inhibitor 0.706 hERG inhibition (predictor II) Inhibitor 0.5549
Spectra
- Mass Spec (NIST)
- Not Available
- Spectra
-
Spectrum Spectrum Type Splash Key Predicted MS/MS Spectrum - 10V, Positive (Annotated) Predicted LC-MS/MS Not Available Predicted MS/MS Spectrum - 20V, Positive (Annotated) Predicted LC-MS/MS Not Available Predicted MS/MS Spectrum - 40V, Positive (Annotated) Predicted LC-MS/MS Not Available Predicted MS/MS Spectrum - 10V, Negative (Annotated) Predicted LC-MS/MS Not Available Predicted MS/MS Spectrum - 20V, Negative (Annotated) Predicted LC-MS/MS Not Available Predicted MS/MS Spectrum - 40V, Negative (Annotated) Predicted LC-MS/MS Not Available
Targets
构建、预测和验证机器学习模型
Use our structured and evidence-based datasets tounlock new
insights and accelerate drug research.
insights and accelerate drug research.
Use our structured and evidence-based datasets to unlock new insights and accelerate drug research.
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Activator
- General Function
- Integrin alpha-5/beta-1 is a receptor for fibronectin and fibrinogen. It recognizes the sequence R-G-D in its ligands. ITGA5:ITGB1 binds to PLA2G2A via a site (site 2) which is distinct from the classical ligand-binding site (site 1) and this induces integrin conformational changes and enhanced ligand binding to site 1 (PubMed:18635536, PubMed:25398877). ITGA5:ITGB1 acts as a receptor for fibrillin-1 (FBN1) and mediates R-G-D-dependent cell adhesion to FBN1 (PubMed:12807887, PubMed:17158881).
- Specific Function
- Epidermal growth factor receptor binding
- Gene Name
- ITGA5
- Uniprot ID
- P08648
- Uniprot Name
- Integrin alpha-5
- 分子Weight
- 114535.52 Da
References
- Vang S, Longley K, Steer CJ, Low WC: The Unexpected Uses of Urso- and Tauroursodeoxycholic Acid in the Treatment of Non-liver Diseases. Glob Adv Health Med. 2014 May;3(3):58-69. doi: 10.7453/gahmj.2014.017. [Article]
- Beuers U: beta1 integrin is a long-sought sensor for tauroursodeoxycholic acid. Hepatology. 2013 Mar;57(3):867-9. doi: 10.1002/hep.26228. [Article]
Enzymes
- Kind
- Protein
- Organism
- Rat
- Pharmacological action
-
Unknown
- 行动
-
Inducer
- General Function
- Testosterone 6-beta-hydroxylase activity
- Specific Function
- Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally un...
- Gene Name
- Cyp3a1
- Uniprot ID
- P04800
- Uniprot Name
- Cytochrome P450 3A1
- 分子Weight
- 57917.375 Da
References
- Paolini M, Pozzetti L, Piazza F, Cantelli-Forti G, Roda A: Bile acid structure and selective modulation of murine hepatic cytochrome P450-linked enzymes. Hepatology. 1999 Sep;30(3):730-9. [Article]
- Kind
- Protein
- Organism
- Rat
- Pharmacological action
-
Unknown
- 行动
-
Inducer
- General Function
- Testosterone 6-beta-hydroxylase activity
- Specific Function
- Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally un...
- Gene Name
- Cyp3a2
- Uniprot ID
- P05183
- Uniprot Name
- Cytochrome P450 3A2
- 分子Weight
- 57731.215 Da
References
- Paolini M, Pozzetti L, Piazza F, Cantelli-Forti G, Roda A: Bile acid structure and selective modulation of murine hepatic cytochrome P450-linked enzymes. Hepatology. 1999 Sep;30(3):730-9. [Article]
Transporters
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Substrate
- General Function
- Sodium-independent organic anion transmembrane transporter activity
- Specific Function
- Mediates the Na(+)-independent transport of organic anions such as sulfobromophthalein (BSP) and conjugated (taurocholate) and unconjugated (cholate) bile acids (By similarity). Selectively inhibit...
- Gene Name
- SLCO1A2
- Uniprot ID
- P46721
- Uniprot Name
- Solute carrier organic anion transporter family member 1A2
- 分子Weight
- 74144.105 Da
References
- Kullak-Ublick GA, Hagenbuch B, Stieger B, Schteingart CD, Hofmann AF, Wolkoff AW, Meier PJ: Molecular and functional characterization of an organic anion transporting polypeptide cloned from human liver. Gastroenterology. 1995 Oct;109(4):1274-82. [Article]
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Substrate
- General Function
- Cystine:glutamate antiporter activity
- Specific Function
- Sodium-independent, high-affinity exchange of anionic amino acids with high specificity for anionic form of cystine and glutamate.
- Gene Name
- SLC7A11
- Uniprot ID
- Q9UPY5
- Uniprot Name
- Cystine/glutamate transporter
- 分子Weight
- 55422.44 Da
References
- Schroeder A, Eckhardt U, Stieger B, Tynes R, Schteingart CD, Hofmann AF, Meier PJ, Hagenbuch B: Substrate specificity of the rat liver Na(+)-bile salt cotransporter in Xenopus laevis oocytes and in CHO cells. Am J Physiol. 1998 Feb;274(2 Pt 1):G370-5. [Article]
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Downregulator
- Curator comments
- This drug-target relationship was established in mice. The significance of this target relationship in humans is unknown.
- General Function
- Protein heterodimerization activity
- Specific Function
- Transporter that appears to play an indispensable role in the selective transport of the dietary cholesterol in and out of the enterocytes and in the selective sterol excretion by the liver into bile.
- Gene Name
- ABCG5
- Uniprot ID
- Q9H222
- Uniprot Name
- ATP-binding cassette sub-family G member 5
- 分子Weight
- 72503.02 Da
References
- Lu Q, Jiang Z, Wang Q, Hu H, Zhao G: The effect of Tauroursodeoxycholic acid (TUDCA) and gut microbiota on murine gallbladder stone formation. Ann Hepatol. 2021 Jul-Aug;23:100289. doi: 10.1016/j.aohep.2020.100289. Epub 2020 Nov 18. [Article]
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Downregulator
- Curator comments
- This drug-target relationship was established in mice. The significance of this target relationship in humans is unknown.
- General Function
- Sterol transporter activity
- Specific Function
- Transporter that appears to play an indispensable role in the selective transport of the dietary cholesterol in and out of the enterocytes and in the selective sterol excretion by the liver into bile.
- Gene Name
- ABCG8
- Uniprot ID
- Q9H221
- Uniprot Name
- ATP-binding cassette sub-family G member 8
- 分子Weight
- 75678.03 Da
References
- Lu Q, Jiang Z, Wang Q, Hu H, Zhao G: The effect of Tauroursodeoxycholic acid (TUDCA) and gut microbiota on murine gallbladder stone formation. Ann Hepatol. 2021 Jul-Aug;23:100289. doi: 10.1016/j.aohep.2020.100289. Epub 2020 Nov 18. [Article]
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
-
Unknown
- 行动
-
Regulator
- Curator comments
- This drug-target relationship was established in mice. The significance of this target relationship in humans is unknown.
- General Function
- Transporter activity
- Specific Function
- Involved in the ATP-dependent secretion of bile salts into the canaliculus of hepatocytes.
- Gene Name
- ABCB11
- Uniprot ID
- O95342
- Uniprot Name
- Bile salt export pump
- 分子Weight
- 146405.83 Da
References
- Lu Q, Jiang Z, Wang Q, Hu H, Zhao G: The effect of Tauroursodeoxycholic acid (TUDCA) and gut microbiota on murine gallbladder stone formation. Ann Hepatol. 2021 Jul-Aug;23:100289. doi: 10.1016/j.aohep.2020.100289. Epub 2020 Nov 18. [Article]
Drug created at February 19, 2013 00:42 / Updated at October 22, 2022 01:06