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Travoprost

Travoprost is used to treat glaucoma and ocular hypertensionis a potent and selective FP prostaglandin receptor agonist. (In Vitro) :Travoprost has sub-micromolar affinity for the DP, EP1, EP3, EP4, IP, and TP receptors. (In Vivo) :Travoprost produces a lower incidence of ocular irritation than PGF20 isopropyl ester at a dose of 1 μg in the New Zealand albino (NZA) rabbit. Topical ocular application of Travoprost produces a marked miotic effect in cats following doses of 0.01, 0.03 and 0.1 μg. In the ocular hypertensive monkey, b.i.d. application of 0.1 and 0.3 μg of travoprost afforded peak reduction in intraocular pressure (IOP) of 22.7% and 28.6%, respectively. Topical application of travoprost was well tolerated in rabbits, cats and monkeys, causing no ocular irritation or discomfort at doses up to 1 μg.

Product Specifications

CAS Number

157283-68-6

Product Name Alternative

Fluprostenol isopropyl ester | AL6221 | Flu-Ipr

Field of Research

Pharmacology & Drug Discovery

Purity

>98% (HPLC)

Solubility

DMSO:41.67 mg/mL (83.25 mM)

Smiles

CC (C) OC (=O) CCC\C=C/CC1C (O) CC (O) C1\C=C\C (O) COc1cccc (c1) C (F) (F) F

Molecular Formula

C26H35F3O6

Molecular Weight

500.55

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

Propan-2-yl (Z) -7-[ (1R2R3R5S) -35-dihydroxy-2-[ (E3R) -3-hydroxy-4-[3- (trifluoromethyl) phenoxy]but-1-enyl]cyclopentyl]hept-5-enoate

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