FLUPROSTENOL
Fluprostenol is a prostaglandin analogue inducing uterine contractions, used in veterinary reproduction. Side effects include sweating, restlessness, and GI upset.
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Product Description
Mechanism of Action
Fluprostenol is a potent prostaglandin F2α analogue that stimulates smooth muscle contraction in reproductive tissues via FP receptors.
Benefits and Advantages
Used in reproductive endocrinology, prostaglandin signalling assays and uterine‑contractility studies.
Side Effects and Risks
Bronchoconstriction, abdominal cramping and hormonal effects.
Datasheet
| Molecular Formula | C23H29F3O6 |
|---|---|
| Molecular Weight | 458.5 g/mol |
| CAS Number | 40666-16-8 |
| Storage Condition | Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light. |
| Solubility | Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance. |
| Purity | Purity information is available upon request (COA). |
| Synonym | fluprostenol; Fluprostenolum; travoprost free acid; Fluoprostenol; ICI 81,008 |
| IUPAC/Chemical Name | (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-enyl]cyclopentyl]hept-5-enoic acid |
| InChl Key | WWSWYXNVCBLWNZ-QIZQQNKQSA-N |
| InChl Code | InChI=1S/C23H29F3O6/c24-23(25,26)15-6-5-7-17(12-15)32-14-16(27)10-11-19-18(20(28)13-21(19)29)8-3-1-2-4-9-22(30)31/h1,3,5-7,10-12,16,18-21,27-29H,2,4,8-9,13-14H2,(H,30,31)/b3-1-,11-10+/t16-,18-,19-,20+,21-/m1/s1 |
| References |
3D Conformer.
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