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首页-小分子抑制剂&激动剂-NF-κB Pathway-TAK1-5Z-7-Oxozeaenol
5Z-7-Oxozeaenol

Chemical Structure : 5Z-7-Oxozeaenol

CAS No.: 253863-19-3

5Z-7-Oxozeaenol ((5Z)-7-Oxozeaenol, TAK1 inhibitor 5ZO, FR148083, LL-Z1640-2)

货号: PC-61198Not For Human Use, Lab Use Only.

5Z-7-Oxozeaenol (5ZO, FR148083) is a potent, selective TAK1 inhibitor with IC50 of 8 nM, displays >33-fold and >62-fold selectivity over MEKK1 and MEKK4 respectively.

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2 mg ¥2980 In stock
5 mg ¥5580 In stock
10 mg ¥8980 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

5Z-7-Oxozeaenol (5ZO, FR148083) is a potent, selective TAK1 inhibitor with IC50 of 8 nM, displays >33-fold and >62-fold selectivity over MEKK1 and MEKK4 respectively.
5Z-7-Oxozeaenol inhibits IL-1-induced activation of NF-κB (IC50= 83 nM) and JNK/p38, inhibits production of inflammatory mediators, and sensitizes cells to TRAIL- and TNF-α-induced apoptosis in vitro.
5Z-7-Oxozeaenol significantly enhances chemotherapeutic efficacy in vivo.

物理化学性质&存储条件

分子量 362.37
分子式 C19H22O7
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(3S,5Z,8S,9S,11E)-3,4,9,10-tetrahydro-8,9,16-trihydroxy-14-methoxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione

参考文献

1. Ninomiya-Tsuji J, et al. J Biol Chem. 2003 May 16;278(20):18485-90.

2. Choo MK, et al. Mol Cancer Ther. 2006 Dec;5(12):2970-6.

3. Sogabe Y, et al. Bioorg Med Chem Lett. 2015 Feb 1;25(3):593-6.

4. Fan Y, et al. Apoptosis. 2013 Oct;18(10):1224-34.

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