(+)-Fluprostenol

Cat. No. 4542

(+)-Fluprostenol C23H29F3O6 [54276-17-4]

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Alternative Name: Travoprost acid

Chemical Name: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-5-heptenoic acid

Biological Activity

Prostaglandin F2α (FP) receptor agonist (Ki = 49.9 nM; EC50 = 2.4 nM). Stimulates intracellular calcium mobilization in cloned human ocular FP receptors, rat A7r5 cells and mouse 3T3 cells (EC50 values are 17.5, 19.1 and 37.3 nM respectively). Analog of prostaglandin F2α. Isopropyl ester travaprost (Cat. No. 4218) also available.

Technical Data

M.Wt:
458.47
Formula:
C23H29F3O6
Solubility:
Soluble in ethanol (supplied pre-dissolved in anhydrous ethanol, 10mg/ml)
Purity:
>95 %
Storage:
Store at -20°C
CAS No:
54276-17-4

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.

Certificate of Analysis / Product Datasheet / Safety Datasheet

References are publications that support the products' biological activity.

Kelly et al (2003) Real-time intracellular Ca2+ mobilization by travoprost acid, bimatoprost, unoprostone, and other analogs via endogenous mouse, rat and cloned human FP prostaglandin receptors. J.Pharmacol.Exp.Ther. 304 238. PMID: 12490597.

Sharif et al (2003) Human trabecular meshwork cell responses induced by bimatoprost, travoprost, unoprostone, and other EP prostaglandin receptor agonist analogues. Invest.Ophthalmol.Vis.Sci. 44 715. PMID: 12556403.

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Keywords: (+)-Fluprostenol, supplier, Travoprost, acid, prostaglandin, F2alpha, F2a, F2α, receptors, agonists, Tocris Bioscience, Prostanoid Receptor Agonist products

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