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P2X3 antagonist 34

カタログ番号GC60281

P2X3 アンタゴニスト 34 は、ヒト P2X3、ラット P2X3、およびモルモット P2X3 受容体に対してそれぞれ 25nM、92nM、および 126nM の IC50 を持つ、強力で選択的かつ経口的に活性な P2X3 ホモ三量体受容体アンタゴニストです。

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P2X3 antagonist 34 化学構造

Cas No.: 2417288-67-4

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5mg
$324.00
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10mg
$556.00
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50mg
$1,576.00
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100mg
$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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