Taurursodiol

CHEMBL272427 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
499.7 g/mol
LogP
3.6
Phase
4

Taurursodiol (sodium phenylbutyrate/ursodoxicoltaurine, also known as AMX0035) is a fixed-dose combination product that modulates endoplasmic reticulum stress and mitochondrial dysfunction, reducing neuronal and motor neuron apoptosis. It is approved for the treatment of amyotrophic lateral sclerosis (ALS) and is under investigation for neurodegenerative diseases. By targeting two complementary pathways of cell death, it offers a novel approach to neuroprotection.

Khối lượng phân tử

499,7000 g/mol

LogP

3,60

TPSA

132,00 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cấu trúc 2D

SVG PNG

Cite this structure


                        

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SMILES

C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C

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

Molecular Formula

C26H45NO6S

HBD / HBA

4 / 6

Liên kết có thể quay

7

Nguyên tử nặng

34

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Câu hỏi thường gặp

Taurursodiol (sodium phenylbutyrate/ursodoxicoltaurine, also known as AMX0035) is a fixed-dose combination product that modulates endoplasmic reticulum stress and mitochondrial dysfunction, reducing neuronal and motor neuron apoptosis. It is approved for the treatment of amyotrophic lateral sclerosis (ALS) and is under investigation for neurodegenerative diseases. By targeting two complementary pathways of cell death, it offers a novel approach to neuroprotection.

Yes, Taurursodiol is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL272427. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9848818. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Tuyên bố miễn trách y tế

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.