- Fluprostenol
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- $1.00
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2019-07-06
- CAS:40666-16-8
- Min. Order: 1kg
- Purity: 95%-99%
- Supply Ability: 100kg
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| | Fluprostenol Basic information |
| Product Name: | Fluprostenol | | Synonyms: | (+/-)-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;FLUPROSTENOL;(±)-16-(3-trifluoromethylphenoxy)tetranorprostaglandin f2α;FLUPROSTENOL, ETHANOL SOLUTION;WWSWYXNVCBLWNZ-QIZQQNKQSA-N;(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 | | CAS: | 40666-16-8 | | MF: | C23H29F3O6 | | MW: | 458.47 | | EINECS: | 255-029-3 | | Product Categories: | prost | | Mol File: | 40666-16-8.mol |  |
| | Fluprostenol Chemical Properties |
| 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| |
| Hazard Codes | F | | Risk Statements | 11 | | Safety Statements | 7-16 | | RIDADR | UN 1170 3/PG 2 | | WGK Germany | 1 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Eye Irrit. 2
Flam. Liq. 2 |
| | Fluprostenol Usage And Synthesis |
| 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. |
| | Fluprostenol Preparation Products And Raw materials |
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