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        產(chǎn)品名稱 JNK-IN-8
        產(chǎn)品貨號 Axon 2361 CAS [1410880-22-6] MF C29H29N7O2MW 507.59 Purity: 98% Soluble in DMSO Description Remarkably potent and selective covalent inhibitor of JNK (IC50 values 4.67 nM, 18.7 nM, and 0.98nM for JNK1/2/3, respectively). JNK-IN-8 inhibits phosphorylation of c-Jun, a direct substrate of JNK, in cells exposed to submicromolar drug in a manner that depends on covalent modification of the conserved cysteine residue (EC50 values 486 nM and 338 nM for inhibition of c-Jun phosphorylation in HeLa and A375 cells, respectively). Useful as a pharmacological probe of JNK-dependent signal transduction References Certificates Categories Extra info T. Zhang et al. Discovery of potent and selective covalent inhibitors of JNK. Chem. Biol. 2012, 19, 140-154. Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Signaling & Oncology CNS Immunology Pain & Inflammation MAPK (JNK) p53-Tumor Suppression NF-κB MAPK EC 2.7.11.24 Remarkably potent and selective covalent inhibitor of JNK Chemical name (E)-3-(4-(dimethylamino)but-2-enamido)-N-(3-methyl-4-(4-(pyridin-3-yl)pyrimidin-2-ylamino)phenyl)benzamide Parent CAS No. [1410880-22-6] Order Size Unit Price Stock 5 mg €120.00 In Stock
        產(chǎn)品價(jià)格 現(xiàn)貨詢價(jià),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

        JNK-IN-8

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

        Axon 2361

        CAS [1410880-22-6]

        MF C29H29N7O2
        MW 507.59

        • Purity: 98%
        • Soluble in DMSO

        JNK-IN-8

        Description

        Remarkably potent and selective covalent inhibitor of JNK (IC50 values 4.67 nM, 18.7 nM, and 0.98nM for JNK1/2/3, respectively). JNK-IN-8 inhibits phosphorylation of c-Jun, a direct substrate of JNK, in cells exposed to submicromolar drug in a manner that depends on covalent modification of the conserved cysteine residue (EC50 values 486 nM and 338 nM for inhibition of c-Jun phosphorylation in HeLa and A375 cells, respectively). Useful as a pharmacological probe of JNK-dependent signal transduction
        Remarkably potent and selective covalent inhibitor of JNK

        Chemical name

        (E)-3-(4-(dimethylamino)but-2-enamido)-N-(3-methyl-4-(4-(pyridin-3-yl)pyrimidin-2-ylamino)phenyl)benzamide

        Parent CAS No.

        [1410880-22-6]

        產(chǎn)品資料
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