Taurursodiol

drug
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Also known as Tauroursodeoxycholic acidTauroursodesoxycholic acidTaurursodiol component of relyvrioUr-906UrsodeoxycholyltaurineUrsodoxicoltaurineUrsodeoxy cholic acidTauroursodeoxycholateTAUROURSODEOXY CHOLIC ACID DIHYDRATETauroursodeoxy cholic_acid dihydrateTauoursodeoxycholic acid

Summary

Taurursodiol (CHEMBL272427) is an approved small-molecule anti-inflammatory agent (ATC A05AA05); indicated across 2 conditions including neurodegenerative disease and amyotrophic lateral sclerosis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: A05AA05
  • Indications: 2 conditions
  • Clinical trials: 17
  • Chemistry: 499.7 Da · C26H45NO6S

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL272427
NameTaurursodiol
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID9848818
ChEBICHEBI:80774
ATCA05AA05
Molecular formulaC26H45NO6S
Molecular weight499.7
InChIKeyBHTRKEVKTKCXOH-LBSADWJPSA-N

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

IUPAC name: 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]ethanesulfonic acid

ChEBI definition: A bile acid taurine conjugate derived from ursoodeoxycholic acid.

Pharmacological roles (ChEBI): anti-inflammatory agent, neuroprotective agent, apoptosis inhibitor, cardioprotective agent, bone density conservation agent.

Other ChEBI roles (chemical / environmental): human metabolite.

Also known as: Tauroursodeoxycholic acid, Tauroursodesoxycholic acid, Taurursodiol, Taurursodiol component of relyvrio, Ur-906, Ursodeoxycholyltaurine, Ursodoxicoltaurine, Ursodeoxy cholic acid, ursodeoxy cholic acid, tauroursodeoxycholic acid, Tauroursodeoxycholate, TAUROURSODEOXY CHOLIC ACID DIHYDRATE

Patent coverage: 1,851 distinct patent families (4,753 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Bile acid receptor, Ileal sodium/bile acid cotransporter, Autotaxin, Phospholipase A2, G-protein coupled bile acid receptor 1.

Bioactivity

ChEMBL activities: 2 potent at pChembl ≥ 5 of 9 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
ENPP27.98IC5010.4nMCHEMBL_ACT_29180045
PLA2G1B5Kd10000nMCHEMBL_ACT_2668845

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
neurodegenerative disease1MONDO:0005559EFO:0005772
amyotrophic lateral sclerosis1MONDO:0004976MONDO:0004976

Clinical trials

Total trials: 17.

Phase distribution

PhaseTrials
Not specified6
PHASE34
PHASE22
PHASE1/PHASE22
PHASE41
PHASE11
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01998451PHASE4UNKNOWNThe Discovery of the Double Sphincter in Gallbladder
NCT01857284PHASE3COMPLETEDSafety and Efficacy of Tauroursodeoxycholic Acid Versus Ursofalk in the Treatment of Adult Primary Biliary Cirrhosis
NCT03481972PHASE3COMPLETEDA Study of Doxycycline and Tauroursodeoxycholic Acid (Doxy/TUDCA) Plus Standard Supportive Therapy Versus Standard Supportive Therapy Alone in Cardiac Amyloidosis Caused by Transthyretin
NCT03800524PHASE3UNKNOWNSafety and Efficacy of TUDCA as add-on Treatment in Patients Affected by ALS
NCT05753852PHASE3UNKNOWNOpen Label Extension of TUDCA-ALS Study
NCT07457632PHASE2NOT_YET_RECRUITINGIntegrative Liver-Targeted Therapy for Diabetic Macular Edema: Combining Tauroursodeoxycholate and Traditional Chinese Medicine.
NCT01171859PHASE2COMPLETEDSafety, Efficacy and Pharmacokinetics of Doxycycline Plus Tauroursodeoxycholic Acid in Transthyretin Amyloidosis
NCT01855360PHASE1/PHASE2COMPLETEDDoxycycline and TUDCA in Patients With Transthyretin Amyloid Cardiomyopathy
NCT03423121PHASE1/PHASE2COMPLETEDA Trial of Bile Acid Supplementation in Patients With Multiple Sclerosis
NCT03878654PHASE1TERMINATEDTrial of Tauroursodeoxycholic Acid (TUDCA) in Asthma
NCT04727320EARLY_PHASE1UNKNOWNThe Clinical Application of Tauroursodeoxycholic Acid in Patients With Liver Fibrosis.
NCT00004410Not specifiedCOMPLETEDRandomized Study of Tauroursodeoxycholic Acid in Prophylactic Therapy of Total Parenteral Nutrition Associated Cholestasis in Infants
NCT00004441Not specifiedCOMPLETEDStudy of Tauroursodeoxycholic Acid for Hepatobiliary Disease in Cystic Fibrosis
NCT00771901Not specifiedCOMPLETEDEffect of Endoplasmic Reticulum Stress on Metabolic Function
NCT01877551Not specifiedCOMPLETEDTauroursodeoxycholic Acid for Protease-inhibitor Associated Insulin Resistance
NCT03331432Not specifiedCOMPLETEDEffects of Dietary Supplement Tauroursodeoxycholic Acid on Vascular Function
NCT03462940Not specifiedTERMINATEDEffects of TUDCA on Endothelial Function in Type 2 DM

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.