ChemicalBook--->CAS DataBase List--->209860-88-8

209860-88-8

209860-88-8 Structure

209860-88-8 Structure
IdentificationBack Directory
[Name]

9ALPHA,11ALPHA-DIHYDROXY-15,15-DIFLUORO-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID
[CAS]

209860-88-8
[Synonyms]

AFP-172
209860-84-1
tafluprost acid
Tafluprost Impurity 9
TAFLUPROST (FREE ACID)
Tafluprost Impurity Tafluprost acid
7-[2-(3,3-difluoro-4-phenoxybut-1-enyl)-3,5-dihydroxycyclopentyl]hept-5-enoic acid
9ALPHA,11ALPHA-DIHYDROXY-15,15-DIFLUORO-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID
(Z)-7-((1R,2R,3R,5S)-2-((E)-3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl)hept-5-enoic acid
5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E)-3,3-difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, (5Z)-
[Molecular Formula]

C22H28F2O5
[MDL Number]

MFCD08062149
[MOL File]

209860-88-8.mol
[Molecular Weight]

410.45
Chemical PropertiesBack Directory
[Boiling point ]

575.9±50.0 °C(Predicted)
[density ]

1.271±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30 mg/ml; DSMO: 30 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 3 mg/ml
[form ]

Oil
[pka]

4.76±0.10(Predicted)
[color ]

Colorless to light yellow
[Optical Rotation]

[α]/D 17 to 22°, c =1.0 in methanol
[InChIKey]

KIQXRQVVYTYYAZ-VKVYFNERSA-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(F)(F)COC1=CC=CC=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H360
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

Tafluprost Acid is a derivative of Tafluprost (T004820), a novel prostanoid used in the treatment of glaucoma and is the first prostanoid to be released in a preservative free-formula.
[Biological Activity]

Taflupost acid is the active metabolite of Tafluprosta prostaglandin F2α agonist th at lowers intraocular pressure and is used in the treatment of glaucoma. Taflupost acid has high affinity and selectivity for the prostaglandin PGF2α (FP) receptor with a Ki of 0.4 nM.
[IC 50]

Human FP Receptor: 0.4 nM (Ki); Human FP Receptor: 0.53 nM (EC50); EP3: 67 nM (IC50)
[storage]

Store at -20°C
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