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        產(chǎn)品名稱 MG 132
        產(chǎn)品貨號 Axon 1869 CAS [133407-82-6] MF C26H41N3O5MW 475.62 Purity: 98% Optical purity: Optically pure Soluble in DMSO Description Specific, potent, reversible, and cell-permeable proteasome inhibitor (Ki = 4 nM). MG132 inhibits NF-κB activation with an IC50 of 3 μM and prevents β-secretase cleavage. MG132 also activates c-Jun N-terminal kinase (JNK1), which initiates apoptosis. References Certificates Categories Extra info D Banerjee and A Liefshitz. Potential of the proteasomal inhibitor MG-132 as an anticancer agent, alone and in combination. Anticancer Res. 2001, 21(6A), 3941-3947. ? VJ Palombella et al. The ubiquitin-proteasome pathway is required for processing the NF-kappa B1 precursor protein and the activation of NF-kappa B. Cell. 1994, 78(5), 773-785. Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Signaling & Oncology MAPK (JNK) Proteasome 26S NF-κB Ubiquitin EC 3.4 Inhibitor of 26S proteasome Chemical name benzyl (S)-4-methyl-1-((S)-4-methyl-1-((S)-4-methyl-1-oxopentan-2-ylamino)-1-oxopentan-2-ylamino)-1-oxopentan-2-ylcarbamate Parent CAS No. [133407-82-6] 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

        MG 132

        Based on 16 reference(s) in Google Scholar 9 10 16

        Axon 1869

        CAS [133407-82-6]

        MF C26H41N3O5
        MW 475.62

        • Purity: 98%
        • Optical purity: Optically pure
        • Soluble in DMSO

        MG 132

        Description

        Specific, potent, reversible, and cell-permeable proteasome inhibitor (Ki = 4 nM). MG132 inhibits NF-κB activation with an IC50 of 3 μM and prevents β-secretase cleavage. MG132 also activates c-Jun N-terminal kinase (JNK1), which initiates apoptosis.
        產(chǎn)品資料
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