Repositioning Candidate Details

Candidate ID: R1159
Source ID: DB08819
Source Type: approved
Compound Type: small molecule
Compound Name: Tafluprost
Synonyms: Tafluprost
Molecular Formula: C25H34F2O5
SMILES: CC(C)OC(=O)CCC\C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1\C=C\C(F)(F)COC1=CC=CC=C1
Structure:
DrugBank Description: A prostaglandin analogue ester prodrug used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension. Chemically, tafluprost is a fluorinated analog of prostaglandin F2-alpha. Tafluprost was approved for use in the U.S. on February 10, 2012.
CAS Number: 209860-87-7
Molecular Weight: 452.5313
DrugBank Indication: Tafluprost is indicated for reducing elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
DrugBank Pharmacology: Tafluprost is a novel prostaglandin analog with a high affinity for the fluoroprostaglandin (FP) receptor PGF2α. Tafluprost has an affinity for the FP receptor that is approximately 12 times higher than that of the carboxylic acid of latanoprost, but with almost no potential to bind to other receptors.
DrugBank MoA: Tafluprost acid is a prostanoid selective FP receptor agonist that is believed to reduce the intraocular pressure (IOP) by increasing the outflow of aqueous humor. Studies in animals and humans suggest that the main mechanism of action is increased uveoscleral outflow.
Targets: Prostaglandin F2-alpha receptor agonist
Inclusion Criteria: Indication associated