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AZD-5069 {[allProObj[0].p_purity_real_show]}

货号:A912767

AZD 5069 is a selective and reversible antagonist of CXCR2 that can inhibit CXCL8 binding to CXCR2 with pIC50 of 9.1.

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
AZD-5069 化学结构 CAS号:878385-84-3
AZD-5069 化学结构
CAS号:878385-84-3
AZD-5069 3D分子结构
CAS号:878385-84-3
AZD-5069 化学结构 CAS号:878385-84-3
AZD-5069 3D分子结构 CAS号:878385-84-3
规格 价格 会员价 库存 数量
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AZD-5069 纯度/质量文件 产品仅供科研

货号:A912767 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 CXCR1 CXCR2 CXCR4 其他靶点 纯度
Reparixin 99%+
SB225002 +++

CXCR2, IC50: 22 nM

99%+
Plerixafor ++

CXCR4, IC50: 44 nM

99%
AMD 3465 6HBr 98%
WZ811 ++++

CXCR4, EC50: 0.3 nM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

AZD-5069 生物活性

描述 AZD-5069 is a CXCR2 antagonist by blocking [125I]-IL-8 binding to human CXCR2 receptors and by inhibiting GROα-induced calcium flux in human neutrophils that are loaded with the fluo-3 dye[1].
体外研究

AZD-5069 is a CXCR2 antagonist by blocking [125I]-IL-8 binding to human CXCR2 receptors and by inhibiting GROα-induced calcium flux in human neutrophils that are loaded with the fluo-3 dye[1].

AZD-5069 动物研究

Dose Mice: 100 mg/kg[1] (i.p.) Cynomolgus monkey: 30 mg/kg - 525 mg/kg[2] (p.o., BID)
Administration i.p., p.o.

AZD-5069 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02499328 Advanced Solid Tumors & Metast... 展开 >>atic Squamous Cell Carcinoma of the Head and Neck 收起 << Phase 1 Phase 2 Recruiting October 31, 2019 -
NCT01962935 Chronic Obstructive Pulmonary ... 展开 >>Disease (COPD). 收起 << Phase 1 Completed - United Kingdom ... 展开 >> Research Site London, United Kingdom 收起 <<
NCT01989520 Uncontrolled and Persistent As... 展开 >>thma 收起 << Phase 1 Completed - United Kingdom ... 展开 >> Research Site London, United Kingdom 收起 <<

AZD-5069 参考文献

[1]Norman P, et al. Evidence on the identity of the CXCR2 antagonist AZD-5069. Expert Opin Ther Pat. 2013 Jan;23(1):113-7.

AZD-5069 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.10mL

0.42mL

0.21mL

10.49mL

2.10mL

1.05mL

20.99mL

4.20mL

2.10mL

AZD-5069 技术信息

CAS号878385-84-3
分子式C18H22F2N4O5S2
分子量 476.518
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

溶解度

DMSO: 95 mg/mL(199.36 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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