99% Min Purity Tafluprost Inhibitor PGF2a Analog Cas 209860-87-7
99% Min Purity Tafluprost Inhibitor PGF2a Analog Cas 209860-87-7
| Product name:Tafluprost | Purity:99% min |
| CAS NO:209860-87-7 | Solubility:DMSO : ≥ 270 mg/mL (596.65 mM) |
| Molecular Formula:C25H34F2O5 | Package:Packaging according to customer requirements |
| Molecular Weight:452.53 | Storage:Store at -20℃ 3 years |
Description:
Travoprost is a PGF2a analog that was launched as an ophthalmic solution administered topically for the treatment of elevated intraocular hypertension as a result of open-angle glaucoma, a common optic neuropathy, and a leading cause of blindness. It can act as an agonist of prostaglandin F receptor.
Targets:
prostaglandin F receptor (HEK-293 cells)
42.3 nM(EC50)
Related Prodcuts:
Latanoprost Lactol; trans-(15S)-Latanoprost; Latanoprostene bunod; 15(S)-Latanoprost; trans-Latanoprost; (+)-Cloprostenol; Cloprostenol; Misoprostol; Carboprost; Tafluprost; Dinoprostone; Dinoprost; Trometamol; Alprostadil; Iloprost; Limaprost; Bimatoprost;
[1]. Kuwayama, Y. and A. Nomura, Prospective observational post-marketing study of tafluprost for glaucoma and ocular hypertension: short-term efficacy and safety. Adv Ther, 2014. 31(4): p. 461-71.
[2]. Kumagami, T., et al., Comparison of corneal safety and intraocular pressure-lowering effect of tafluprost ophthalmic solution with other prostaglandin ophthalmic solutions. J Ocul Pharmacol Ther, 2014. 30(4): p. 340-5.
[3]. Inoue, K., A. Tanaka, and G. Tomita, Effects of tafluprost treatment for 3 years in patients with normal-tension glaucoma. Clin Ophthalmol, 2013. 7: p. 1411-6.
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