Powder: -20°C for 3 years | In solvent: -80°C for 1 year
(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
5 mg | 35 days | $ 798.00 | |
10 mg | 35 days | $ 1,410.00 |
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 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ethanol: 50 mg/mL (117.67 mM), Sonication is recommended.
DMSO: 100 mg/mL (235.34 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. More
bottom
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
(+)-Cloprostenol 54276-21-0 Others (+)Cloprostenol D-Cloprostenol Cloprostenol (+) Cloprostenol inhibitor inhibit