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Latanoprost (free acid) (Synonyms: LatFA, 17phenyl13,14dihydro trinor Prostaglandin F2α, PhXA85)

Catalog No.GC41229

Le latanoprost (acide libre), un analogue de la prostaglandine (PG) F2α, est un agoniste sélectif des récepteurs prostanoÏdes (FP) qui active spécifiquement le récepteur FP-PG.

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Latanoprost (free acid) Chemical Structure

Cas No.: 41639-83-2

Taille Prix Stock Qté
1mg
94,00 $US
En stock
5mg
425,00 $US
En stock
10mg
754,00 $US
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50mg Please Inquire Please Inquire

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Latanoprost is an F-series prostaglandin (PG) analog which has been approved for use as an ocular hypotensive drug. Latanoprost is an isopropyl ester, a prodrug form which is converted to latanoprost (free acid) by endogenous esterase enzymes. The free acid form is 200 times more potent than latanoprost as an FP receptor ligand for the human recombinant FP receptor. Latanoprost is the isopropyl ester of a PGF2α analog containing an aromatic group (17-phenyl) in the ω-chain. Lat-FA is the corresponding carboxylic acid of this analog. Lat-FA is a potent FP receptor agonist with an EC50 of 3.6 nM for human FP receptors, which is twice the potency of PGF2α. The efficacy of PG analog esters for the treatment of glaucoma correlates closely with the FP receptor binding affinity of the free acid. However, Lat-FA is more irritating and less effective than the prodrug latanoprost when applied directly to the eyes of human glaucoma patients.

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Average Rating: 5 ★★★★★ (Based on Reviews and 39 reference(s) in Google Scholar.)

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