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(+)-Cloprostenol
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Catalog No. T13461Cas No. 54276-21-0
Alias D-Cloprostenol
(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.
(+)-Cloprostenol
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Catalog No. T13461Alias D-CloprostenolCas No. 54276-21-0
(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $798 | 35 days | |
| 10 mg | $1,410 | 35 days |
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Product Introduction
Bioactivity
Chemical Properties
| 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]. |
| Alias | D-Cloprostenol |
| Molecular Weight | 424.92 |
| Formula | C22H29ClO6 |
| Cas No. | 54276-21-0 |
| Relative Density. | 1.31g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| 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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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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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
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