CAS NO: | 345303-91-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
AZD9056 hydrochloride is a selective orally active inhibitor ofP2X7which plays a significant role in inflammation and pain-causing diseases. |
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体外研究 (In Vitro) |
The antagonist AZD9056 blocks P2X7 receptors with an IC50of 11.2 nM in HEK-hP2X7 cell line, indicating a high selectivity of the antagonist for the P2X7 receptor. The P2X7-receptor antagonist AZD9056 has a clear inhibitory effect (IC50=1-3 μM) in mouse microglia BV2 cells[1]. AZD9056 is an inhibitor of BCRP and weakly inhibits BCRP-mediated transport of methotrexate (IC50=92 μM)[2].
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体内研究 (In Vivo) |
Treatment with AZD9056 exerts pain-relieving and anti-inflammatory effects. The upregulated expression of interleukin (IL)-1β, IL-6, tumor necrosis factor-α (TNF-α), matrix metalloproteinase-13 (MMP-13), substance P (SP) and prostaglandin E2 (PGE2) which is induced by MIA in cartilage tissues is reversed by AZD9056[3].
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Clinical Trial |
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分子量 |
455.46 |
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性状 |
Solid |
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Formula |
C24H36Cl2N2O2 |
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CAS 号 |
345303-91-5 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:
DMSO : 50 mg/mL(109.78 mM;Need ultrasonic) H2O : 1.67 mg/mL(3.67 mM;ultrasonic and warming and heat to 60℃)
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