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P2X3 antagonist 34

Catalog No.GC60281

P2X3 길항제 34는 인간 P2X3, 쥐 P2X3 및 기니피그 P2X3 수용체에 대해 IC50이 각각 25nM, 92nM 및 126nM인 강력하고 선택적이고 경구 활성인 P2X3 동종삼량체 수용체 길항제입니다.

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P2X3 antagonist 34 Chemical Structure

Cas No.: 2417288-67-4

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5mg
US$324.00
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10mg
US$556.00
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50mg
US$1,576.00
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100mg
US$2,410.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

P2X3 antagonist 34 is a potent, selective and orally active P2X3 homotrimeric receptor antagonist with IC50s of 25?nM, 92?nM and 126?nM for human P2X3, rat P2X3 and guinea pig P2X3 receptors, respectively. P2X3 antagonist 34 is less active against human, rat and guinea pig P2X2/3 heterotrimeric receptors. P2X3 antagonist 34 has strong anti-tussive effect[1].

P2X3 antagonist 34 (BLU-5937; 500?nM) is able to block αβ-meATP-induced sensitization and firing activity of isolated primary nociceptors in rat dorsal root ganglions (DRGs), through P2X3 homotrimeric receptor antagonism. The sensitizing effect of αβ-meATP and the inhibition of P2X3 antagonist 34 are reversible after washout[1].

P2X3 antagonist 34 (BLU-5937; 0.3-0mg/kg, oral administration; male Dunkin Hartley guinea pigs) treatment significantly reduces the histamine-induced enhancement in the number of citric acid-induced coughs in a dose-dependent fashion in a guinea pig cough model[1].P2X3 antagonist 34 (BLU-5937; 3 and 30mg/kg, oral) is also shown to reduce significantly and dose-dependently the ATP-induced enhancement of citric acid-induced coughs in the guinea pig[1]. Animal Model: Male Dunkin Hartley guinea pigs[1]

[1]. Garceau D, et al. BLU-5937: A selective P2X3 antagonist with potent anti-tussive effect and no taste alteration. Pulm Pharmacol Ther. 2019 Jun;56:56-62.

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