Chemical Structure : Ceapin-A7
CAS No.: 2323027-38-7
货号: PC-73217Not For Human Use, Lab Use Only.
Ceapin-A7 is a selective inhibitor of ATF6α with IC50 of 0.59 uM, selective over ATF6β, PERK and other branches of the unfolded protein response (UPR).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥680 | In stock | |
10 mg | ¥980 | In stock | |
25 mg | ¥1680 | In stock | |
50 mg | ¥2680 | In stock | |
100 mg | Get quote |
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Ceapin-A7 is a selective inhibitor of ATF6α with IC50 of 0.59 uM, selective over ATF6β, PERK and other branches of the unfolded protein response (UPR).
Ceapin-A7 inhibits ER stress-induced upregulation of BiP in vitro.
Ceapin-A7 inhibits cleavage and functional activation of endogenous ATF6 in response to ER stress in vitro.
Ceapin-A7 could phenocopy the results obtained using genetic ablation of ATF6α in mouse models.
Ceapin-A7 is a first-in-class series of ATF6α inhibitors that selectively blocks ATF6α and not ATF6β, SREBP or other UPR branches.
分子量 | 470.33 | |
分子式 | C20H12F6N4O3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
N-(1-(2,4-Bis(trifluoromethyl)benzyl)-1H-pyrazol-4-yl)-5-(furan-2-yl)isoxazole-3-carboxamide |
1. Ciara M Gallagher, et al. eLife. 2016; 5: e11878.
2. Mufrrih M, et al. mSphere. 2021 Jun 30;6(3):e0036121.
3. Ma M, et al. iScience. 2021 Jun 28;24(7):102791.
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