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(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $1,150 | 35 days | 35 days | |
| 10 mg | $1,980 | 35 days | 35 days |
| Description | (+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic. |
| In vitro | D-Closrostenol and PGF2α have the same potency. In inhibiting the binding of [3H] PGF2α to the corpus luteum membrane, its potency is about 150 times that of dl-cloprostenol (P<0.05), and its potency is about 280 times that of PGE1. However, in myometrial cell membranes, d-cloprostenol and PGF2 alpha are about 10 times more potent than dl-cloprostenol and 95 times more potent than PGE1[2]. |
| Synonyms | D-Cloprostenol |
| Molecular Weight | 424.92 |
| Formula | C22H29ClO6 |
| Cas No. | 54276-21-0 |
| Smiles | O[C@@H](COc1cccc(Cl)c1)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O |
| Relative Density. | 1.31g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | Ethanol: 50 mg/mL (117.67 mM), Sonication is recommended. DMSO: 100 mg/mL (235.34 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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