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ChemicalBook--->CAS DataBase List--->40666-16-8

40666-16-8

40666-16-8 Structure

40666-16-8 Structure
IdentificationBack Directory
[Name]

Fluprostenol
[CAS]

40666-16-8
[Synonyms]

FLUPROSTENOL
WWSWYXNVCBLWNZ-QIZQQNKQSA-N
FLUPROSTENOL, ETHANOL SOLUTION
Travoprost Impurity 31((±)-Fluprostenol)
(±)-16-(3-trifluoromethylphenoxy)tetranorprostaglandin f2α
(+/-)-16-(3-TRIFLUOROMETHYLPHENOXY)TETRANORPROSTAGLANDIN F2ALPHA
(+/-)16-(M-TRIFLUOROMETHYLPHENOXY)-TETRANOR-PROSTAGLANDIN F2ALPHA
(+/-)-9ALPHA,11ALPHA,15R-TRIHYDROXY-16-(3-(TRIFLUOROMETHYL)PHENOXY)-17,18,19, 20-TETRANORPROSTA 5Z,13E-DIEN-1-OIC ACID
(5Z)-rel-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-butenyl]cyclopentyl]-5-heptenoic acid
5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]cyclopentyl]-, (5Z)-rel-
[EINECS(EC#)]

255-029-3
[Molecular Formula]

C23H29F3O6
[MDL Number]

MFCD03427566
[MOL File]

40666-16-8.mol
[Molecular Weight]

458.47
Chemical PropertiesBack Directory
[Boiling point ]

608.0±55.0 °C(Predicted)
[density ]

1.335
[storage temp. ]

−20°C
[form ]

Colorless oil dissolved in ethanol (1mg/100μl).
[pka]

4.76±0.10(Predicted)
[InChIKey]

WWSWYXNVCBLWNZ-QAAGTRDINA-N
[SMILES]

C(O)(=O)CCC/C=C\C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)COC1=CC=CC(C(F)(F)F)=C1 |&1:9,10,13,15,18,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P305+P351+P338
[Hazard Codes ]

F
[Risk Statements ]

11
[Safety Statements ]

7-16
[RIDADR ]

UN 1170 3/PG 2
[WGK Germany ]

1
Hazard InformationBack Directory
[Uses]

Fluprostenol is a prostaglandin F (FP) receptor agonist.
[Definition]

ChEBI: Fluprostenol is an organofluorine compound that is racemic prostaglandin F2alpha in which the pentyl group is replaced by a 3-(trifluoromethyl)phenoxymethyl group. A synthetic analogue of prostaglandin F2alpha, ophthalmic solutions of its isopropyl ester prodrug, travoprost, are used as a topical medication for controlling the progression of open-angle glaucoma and ocular hypertension, by reducing intraocular pressure. The isopropyl ester group of travoprost is hydrolysed to the biologically active free acid by esterases in the cornea. It has a role as an antiglaucoma drug, an antihypertensive agent, a prostaglandin receptor agonist, a female contraceptive drug and an abortifacient. It is a prostaglandins Falpha, a hydroxy monocarboxylic acid and a member of (trifluoromethyl)benzenes.
[Biological Activity]

Fluprostenol is a selective prostaglandin F2-α (PGF2α) receptor or prostaglandin F (FP) receptor agonist.
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