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5-BDBD

Catalog No. T22518   CAS 768404-03-1

5-BDBD is a potent and selective P2X4 receptor antagonist. 5-BDBD inhibits rP2X4R-mediated currents with an IC50 of 0.75 μM. 5-BDBD completely blocked the basal and acute hyperalgesia induced by NTG.

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5-BDBD Chemical Structure
5-BDBD, CAS 768404-03-1
Pack Size Availability Price/USD Quantity
1 mg In stock $ 36.00
2 mg In stock $ 52.00
5 mg In stock $ 84.00
10 mg In stock $ 147.00
25 mg In stock $ 322.00
50 mg In stock $ 572.00
100 mg In stock $ 815.00
1 mL * 10 mM (in DMSO) In stock $ 94.00
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Purity: 99.74%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description 5-BDBD is a potent and selective P2X4 receptor antagonist. 5-BDBD inhibits rP2X4R-mediated currents with an IC50 of 0.75 μM. 5-BDBD completely blocked the basal and acute hyperalgesia induced by NTG.
Targets&IC50 P2X4:0.75 μM
In vitro 5-BDBD could be specifically used to discriminate between P2X1R, P2X2aR, P2X2bR, P2X3R, P2X4R, and P2X7R[1]. 5-BDBD inhibits 10 μM ATP-induced currents of rP2X4R-expressing HEK293 cells in a concentration-dependent manner, with an IC50 of 0.75 μM[1]. 5-BDBD displaces rightward the ATP concentration-response curve, with an EC50 of 4.7 to 15.9 μM[1].
In vivo Basal hyperalgesia induced by recurrent NTG injection was completely blocked by 5-BDBD[2].
Animal Research 5-BDBD (28 mg/kg; i.p.; daily for 9 days; male C57BL/6 mice) prevented NTG-induced mechanical hypersensitivity[2].
Molecular Weight 355.19
Formula C17H11BrN2O2
CAS No. 768404-03-1

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 60 mg/mL (168.92 mM), Sonication and heating to 60℃ are recommended.

TargetMolReferences and Literature

1. Coddou C, et al. Characterization of the antagonist actions of 5-BDBD at the rat P2X4 receptor. Neurosci Lett. 2019;690:219-224. 2. Long T, et al. Microglia P2X4 receptor contributes to central sensitization following recurrent nitroglycerin stimulation. J Neuroinflammation. 2018;15(1):245. Published 2018 Aug 30.

Related compound libraries

This product is contained In the following compound libraries:
Membrane Protein-targeted Compound Library Inhibitor Library Ion Channel Inhibitor Library Bioactive Compounds Library Max Anti-Cancer Compound Library Neuronal Signaling Compound Library NO PAINS Compound Library Bioactive Compound Library

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Keywords

5-BDBD 768404-03-1 Membrane transporter/Ion channel Neuroscience P2X Receptor inhibit P2XRs currents NTG hyperalgesia selective Inhibitor ATP 5BDBD acute 5 BDBD inhibitor

 

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