Tafluprost

CHEMBL1963683 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
452.5 g/mol
LogP
4.5
Phase
4

Tafluprost is a fluorinated prostanoid analog of latanoprost, a selective prostaglandin FP receptor agonist used as a preservative-free ophthalmic solution for reduction of elevated intraocular pressure (IOP) in open-angle glaucoma and ocular hypertension. By increasing uveoscleral outflow of aqueous humor through FP receptor activation on ciliary smooth muscle, it reduces IOP without affecting aqueous humor production. The preservative-free formulation is particularly beneficial for patients with ocular surface disease.

分子量

452.5000 g/mol

LogP

4.50

TPSA

76.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

2D構造

SVG PNG

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SMILES

CC(C)OC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/C(F)(F)COc2ccccc2)[C@H](O)C[C@@H]1O

InChI

InChI=1S/C25H34F2O5/c1-18(2)32-24(30)13-9-4-3-8-12-20-21(23(29)16-22(20)28)14-15-25(26,27)17-31-19-10-6-5-7-11-19/h3,5-8,10-11,14-15,18,20-23,28-29H,4,9,12-13,16-17H2,1-2H3/b8-3-,15-14+/t20-,21-,22+,23-/m1/s1

Molecular Formula

C25H34F2O5

HBD / HBA

2 / 7

回転可能結合数

13

重原子数

32

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.

よくある質問

Tafluprost is a fluorinated prostanoid analog of latanoprost, a selective prostaglandin FP receptor agonist used as a preservative-free ophthalmic solution for reduction of elevated intraocular pressure (IOP) in open-angle glaucoma and ocular hypertension. By increasing uveoscleral outflow of aqueous humor through FP receptor activation on ciliary smooth muscle, it reduces IOP without affecting aqueous humor production. The preservative-free formulation is particularly beneficial for patients with ocular surface disease.

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Yes, Tafluprost 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). CHEMBL1963683. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9868491. Chemical information database.

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

医学的免責事項

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.