Tafluprost

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ChongDa Prostaglandin Fine Chemicals Co., Ltd

Business Type:Manufacturer

Country/Region:China

Ddu Verified

HOT Rank

8/10

Product Information

  • Chemical Formula:C25H34F2O5
  • Molecular Weight:452.53
  • Assay:Purity HPLC ≥98%
  • Pharmacopeia:CP
  • Shelf Life:18 months
  • Storage:Sealed

Description

Tafluprost (MK2452, AFP-168) is a selective prostaglandin F (FP) receptor agonist that effectively lowers intraocular pressure (IOP) in preclinical models. In studies using normotensive and glaucomatous rabbits and monkeys, topical administration of tafluprost reduced IOP by 25–35%, demonstrating dose-dependent ocular hypotensive activity. It enhanced uveoscleral outflow with high receptor selectivity and minimal off-target effects, while showing efficient corneal penetration and sustained ocular residence. Pharmacokinetic analyses indicated low systemic exposure, reducing potential side effects. These findings support tafluprost’s potential as a safe and effective therapy for glaucoma and ocular hypertension, providing sustained IOP reduction and protection against optic nerve damage.

Tafluprost (AFP-168) is an anti-glaucoma prostaglandin (PG) analog. Tafluprost can inhibit the apoptosis of retinal ganglion cells (RGCs) and rat RGCs cells. Tafluprost promotes axon regeneration by regulating Zn2+-mTOR pathway, inhibits intracellular lipid accumulation in human preorbital adipocytes. Tafluprost can be used in the study of optic nerve injury in glaucoma.



Appearance

pale yellow to colorless Oil

Identification

NMR HPLC

Optical Rotation(C=0.5 ethanol)

+19.0° ~ +23°

Water

≤ 1.0%

Related substances

Tafluprost acid≤ 0.3%
5,6-trans isomer ≤ 0.5 %
Any unspecified impurity:≤0.1 %
Total impurities:≤2.0 %

Residue Solvent

n-Hexane:≤0.029%
Isopropanol:≤0.5%
Methyl tert-butyl ether:≤0.5%
N,N-Dimethylformamide≤ 0.088%

Purity by HPLC

≥98%


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