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BW 245C

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Catalog No. T14842Cas No. 72814-32-5
Alias BW245C

BW 245C is a selective prostaglandin-like DP receptor (DP1) agonist, a prostaglandin analogue with inhibitory effects on the aggregation response of collagen, which can be used to study diseases such as stroke.

BW 245C

BW 245C

🥰Excellent
Catalog No. T14842Alias BW245CCas No. 72814-32-5
BW 245C is a selective prostaglandin-like DP receptor (DP1) agonist, a prostaglandin analogue with inhibitory effects on the aggregation response of collagen, which can be used to study diseases such as stroke.
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1 mg$199In Stock
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Purity:≥99%
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Product Introduction

Bioactivity
Description
BW 245C is a selective prostaglandin-like DP receptor (DP1) agonist, a prostaglandin analogue with inhibitory effects on the aggregation response of collagen, which can be used to study diseases such as stroke.
In vitro
The prostaglandin DP receptor agonist BW 245C (0.01-1μM) inhibited TGF-β-induced collagen secretion and increased intracellular cAMP in lung fibroblasts [3]. The use of the DP receptor agonist BW 245C (0.1-3μmol/L) dose-dependently increased the transendothelial resistance of human umbilical vein endothelial cells and decreased FITC-dextran permeability. Moreover, it elevated intracellular cAMP levels and subsequent protein kinase A (PKA) activity [4].
In vivo
Injection of the DP1 agonist BW 245C (100 nM, 20 uL) did not significantly increase MBP-positive eosinophils in the esophageal epithelial cells of OVA-sensitized guinea pigs [2]. WT and DP1 (-/-) mice underwent middle cerebral artery occlusion, followed by a single intraperitoneal injection of vehicle or 0.02, 0.2, or 2.0 mg/kg BW 245C, and then immediate reperfusion. The results showed that BW 245C treatment significantly increased baseline CBF in WT mice but not in DP1 (-/-) mice [1].
AliasBW245C
Chemical Properties
Molecular Weight368.47
FormulaC19H32N2O5
Cas No.72814-32-5
SmilesC(C[C@@H](O)C1CCCCC1)N2[C@@H](CCCCCCC(O)=O)C(=O)NC2=O
Relative Density.1.167 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 30 mg/mL (81.42 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7139 mL13.5696 mL27.1393 mL135.6963 mL
5 mM0.5428 mL2.7139 mL5.4279 mL27.1393 mL
10 mM0.2714 mL1.3570 mL2.7139 mL13.5696 mL
20 mM0.1357 mL0.6785 mL1.3570 mL6.7848 mL
50 mM0.0543 mL0.2714 mL0.5428 mL2.7139 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent 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 DMSOTargetMol | reagent (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 DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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