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BzATP triethylammonium salt

BzATP triethylammonium salt
BzATP triethylammonium salt is a P2X7 receptor agonist.
Catalog No. TP2226Cas No. 112898-15-4
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Purity:96.26%
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BzATP triethylammonium salt

Catalog No. TP2226Cas No. 112898-15-4

BzATP triethylammonium salt is a P2X7 receptor agonist.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$41In Stock
5 mg$97In Stock
10 mg$155In Stock
25 mg$258In Stock
1 mL x 10 mM (in DMSO)$179In Stock
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Product Introduction

Bioactivity
Description
BzATP triethylammonium salt is a P2X7 receptor agonist.
In vitro
METHODS: Glioma cell lines U87 and U251 were treated with BzATP triethylammonium salt (5-1000 µM) for 2-72 h. Cell proliferation was detected by MTT assay.
RESULTS: Proliferation of glioma cell lines U87 and U251 was significantly increased in the presence of BzATP. the peak fine cell proliferation of both U87 and U251 cell lines was 100 µM BzATP, and the optimal incubation time was 24 h for both cell lines [1].
METHODS: Retinal ganglion cells were treated with BzATP triethylammonium salt (50 µM) for 2 min and intracellular Ca2+ levels were measured.
RESULTS: The P2X7 agonist BzATP resulted in a rapid increase in intracellular Ca2+ and the level remained elevated for 2 min after agonist application. More than 80% of the examined cells responded strongly to BzATP. [2]
In vivo
METHODS: To investigate the effects on whole-body energy metabolism, BzATP triethylammonium salt (1 mg/kg) was administered intraperitoneally to C57BL/6J mice once daily for seven days.
RESULTS: BzATP triethylammonium salt increased metabolic rate and O2 consumption while decreasing respiratory rate and upregulating NADPH oxidase 2 in gastrocnemius and tibialis anterior muscle.The findings suggest that activation of P2X7 has a significant effect on energy homeostasis and muscle metabolism. [3]
Chemical Properties
Molecular Weight1018.96
FormulaC24H24N5O15P3·C18H45N3
Cas No.112898-15-4
Storage & Solubility Information
Storagestore at low temperature,keep away from moisture,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 50 mg/mL (49.06 mM), Sonification is recommended.
DMSO: 50 mg/mL (49.06 mM), Sonification is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM0.9814 mL4.9070 mL9.8139 mL49.0696 mL
5 mM0.1963 mL0.9814 mL1.9628 mL9.8139 mL
10 mM0.0981 mL0.4907 mL0.9814 mL4.9070 mL
20 mM0.0491 mL0.2453 mL0.4907 mL2.4535 mL

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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:
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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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