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        產(chǎn)品名稱 ISRIB - trans-ISRIB
        產(chǎn)品貨號 Axon 2278 CAS [1597403-47-8] MF C22H24Cl2N2O4MW 451.34 Purity: 99% Optical purity: Relative stereochemistry Soluble in DMSO and DCM-MeOH Description First reported, potent and selective inhibitor of the ‘integrated stress response’ (ISR) and a potent inhibitor of PERK signaling. ISRIB potently reverses the effects of eIF2α phosphorylation (IC50 value of 5 nM for inhibition of ATF4-luciferase reporter).Trans-ISRIB reduces the viability of cells subjected to PERK-activation by chronic endoplasmic reticulum stress, and proved to be 100-fold more potent than cis-ISRIB, indicating that the compound’s interaction with its cellular target is stereospecific. References Certificates Categories Extra info C. Sidrauski et al. Pharmacological brake-release of mRNA translation enhances cognitive memory. eLife 2013, 2, e00498. ? A.G. Hinnebusch et al. Cell biology. Blocking stress response for better memory? Science. 2015 May 29;348(6238):967-8. Certificate of Analysis Material Safety Data Sheet Angiogenesis Cell Signaling & Oncology CNS PERK EC 2.7.11.1 Potent inhibitor of the integrated stress response and PERK signaling Chemical name N,N'-((1r,4r)-cyclohexane-1,4-diyl)bis(2-(4-chlorophenoxy)acetamide) Parent CAS No. [1597403-47-8] Order Size Unit Price Stock 10 mg €95.00 In Stock
        產(chǎn)品價格 現(xiàn)貨詢價,電話:010-67529703
        產(chǎn)品規(guī)格
        產(chǎn)品品牌 axonmedchem
        產(chǎn)品概述
        產(chǎn)品詳情

        ISRIB - trans-ISRIB

        Based on 14 reference(s) in Google Scholar 8 10 14

        Axon 2278

        CAS [1597403-47-8]

        MF C22H24Cl2N2O4
        MW 451.34

        • Purity: 99%
        • Optical purity: Relative stereochemistry
        • Soluble in DMSO and DCM-MeOH

        ISRIB

        Description

        First reported, potent and selective inhibitor of the ‘integrated stress response’ (ISR) and a potent inhibitor of PERK signaling. ISRIB potently reverses the effects of eIF2α phosphorylation (IC50 value of 5 nM for inhibition of ATF4-luciferase reporter).Trans-ISRIB reduces the viability of cells subjected to PERK-activation by chronic endoplasmic reticulum stress, and proved to be 100-fold more potent than cis-ISRIB, indicating that the compound’s interaction with its cellular target is stereospecific.
        產(chǎn)品資料
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