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Zapnometinib {[allProObj[0].p_purity_real_show]}

货号:A578981 同义名: PD0184264;ATR-002 Ambeed 开学季,买赠积分,赢豪礼

Zapnometinib is a MEK inhibitor, with an IC50 of 5.7 nM.

Zapnometinib 化学结构 CAS号:303175-44-2
Zapnometinib 化学结构
CAS号:303175-44-2
Zapnometinib 3D分子结构
CAS号:303175-44-2
Zapnometinib 化学结构 CAS号:303175-44-2
Zapnometinib 3D分子结构 CAS号:303175-44-2
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Zapnometinib 纯度/质量文件 产品仅供科研

货号:A578981 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 MEK MEK1 MEK1/2 MEK2 MEK5 其他靶点 纯度
Honokiol {[allProObj[0].p_purity_real_show]}
Mirdametinib ++++

MEK, IC50: 0.33 nM

{[allProObj[0].p_purity_real_show]}
Binimetinib +++

MEK, IC50: 12 nM

{[allProObj[0].p_purity_real_show]}
BI-847325 ++

MEK1, IC50: 25 nM

+++

MEK2, IC50: 4 nM

{[allProObj[0].p_purity_real_show]}
U0126-EtOH +

MEK1, IC50: 0.07 μM

++

MEK2, IC50: 0.06 μM

{[allProObj[0].p_purity_real_show]}
GDC-0623 ++++

MEK1, IC50: 0.13 nM

{[allProObj[0].p_purity_real_show]}
TAK-733 ++++

MEK1, IC50: 3.2 nM

{[allProObj[0].p_purity_real_show]}
Trametinib ++++

MEK1, IC50: 0.92 nM

++++

MEK2, IC50: 1.8 nM

{[allProObj[0].p_purity_real_show]}
Selumetinib +++

MEK1, Kd: 99 nM

MEK1, IC50: 14 nM

+

MEK2, Kd: 530 nM

{[allProObj[0].p_purity_real_show]}
CI-1040 ++

MEK1, IC50: 17 nM

++

MEK2, IC50: 17 nM

{[allProObj[0].p_purity_real_show]}
Myricetin {[allProObj[0].p_purity_real_show]}
Refametinib ++

MEK1, IC50: 19 nM

++

MEK2, IC50: 47 nM

{[allProObj[0].p_purity_real_show]}
Cobimetinib +++

MEK1, IC50: 4.2 nM

{[allProObj[0].p_purity_real_show]}
PD98059 +

MEK1, IC50: 2 μM

{[allProObj[0].p_purity_real_show]}
SL327 +

MEK1, IC50: 0.18 μM

+

MEK2, IC50: 0.22 μM

AP-1 {[allProObj[0].p_purity_real_show]}
PD318088 {[allProObj[0].p_purity_real_show]}
AZD8330 +++

MEK1/2, IC50: 7 nM

{[allProObj[0].p_purity_real_show]}
Pimasertib {[allProObj[0].p_purity_real_show]}
(E/Z)-BIX02189 ++++

MEK5, IC50: 1.5 nM

{[allProObj[0].p_purity_real_show]}
(E/Z)-BIX02188 +++

MEK5, IC50: 4.3 nM

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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。

Zapnometinib 生物活性

描述 Zapnometinib (PD0184264), a MEK inhibitor and active metabolite of CI-1040, displays an IC50 of 5.7 nM. It demonstrates antiviral activity against influenza virus and antibacterial effects [1][2][3].
体内研究

In mice infected with lethal H1N1pdm09, Zapnometinib (8.4-75 mg/kg/day; administered orally three times a day) lowers lung virus titers and improves survival rates [1].

Zapnometinib (150 mg/kg) yields AUC values of 860.02 and 1953.68 μg•h/mL in mice via intravenous or oral administration, respectively [1].

体外研究

Zapnometinib (0.1 nM-1 μM) inhibits MEK, showing IC50 values of 30.96 nM, 357 nM, and 15 nM in cell-free kinase assay, A549, MDCK cells, and human PBMCs [1].

Zapnometinib (100 μM; 4 h) impedes Ionomycin-induced phosphorylation of ERK1/2 in human PBMCs [1].

Zapnometinib (1-100 μM) decreases the viral titers of IV H1N1pdm09 and H3N2 [1].

Zapnometinib 参考文献

[1]Laure M, et, al. Antiviral efficacy against influenza virus and pharmacokinetic analysis of a novel MEK-inhibitor, ATR-002, in cell culture and in the mouse model. Antiviral Res. 2020 Jun;178:104806.

[2]Hamza H, et, al. Improved in vitro Efficacy of Baloxavir Marboxil Against Influenza A Virus Infection by Combination Treatment With the MEK Inhibitor ATR-002. Front Microbiol. 2021 Feb 12;12:611958.

[3]Bruchhagen C, et, al. Metabolic conversion of CI-1040 turns a cellular MEK-inhibitor into an antibacterial compound. Sci Rep. 2018 Jun 14;8(1):9114.

Zapnometinib 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.44mL

0.49mL

0.24mL

12.21mL

2.44mL

1.22mL

24.42mL

4.88mL

2.44mL

Zapnometinib 技术信息

CAS号303175-44-2
分子式C13H7ClF2INO2
分子量 409.555
别名 PD0184264;ATR-002
运输蓝冰
存储条件

粉末 Keep in dark place,Sealed in dry,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 60 mg/mL(146.5 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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