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        產(chǎn)品名稱 Nexturastat A
        產(chǎn)品貨號(hào) Axon 2359 CAS [1403783-31-2] MF C19H23N3O3MW 341.40 Purity: 99% Soluble in DMSO Description Potent HDAC6 inhibitor with >600 fold and >190 fold selectivity over HDAC1 and HDAC8, respectively (IC50 values 5 nM, 3 μM, 1 μM for HDAC6, HDAC1, and HDAC8, respectively). Nexturastat A was found to be capable of increasing acetylated α-tubulin levels and it inhibited the growth of B16 melanoma cells, albeit with lower potency than LBH 589 (Axon 1548). References Certificates Categories Extra info J.A. Bergman et al. Selective histone deacetylase 6 inhibitors bearing substituted urea linkers inhibit melanoma cell growth. J. Med. Chem. 2012, 55, 9891-9899. Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Cycle Regulation Cell Signaling & Oncology Epigenetics DNA-damage Response EC 3.5.1.98 HDAC HDAC6 inhibitor with good selectivity over HDAC1 and HDAC8 Chemical name 4-((1-butyl-3-phenylureido)methyl)-N-hydroxybenzamide Parent CAS No. [1403783-31-2] Order Size Unit Price Stock 5 mg €95.00 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

        Nexturastat A

        Based on 12 reference(s) in Google Scholar 9 10 12

        Axon 2359

        CAS [1403783-31-2]

        MF C19H23N3O3
        MW 341.40

        • Purity: 99%
        • Soluble in DMSO

        Nexturastat A

        Description

        Potent HDAC6 inhibitor with >600 fold and >190 fold selectivity over HDAC1 and HDAC8, respectively (IC50 values 5 nM, 3 μM, 1 μM for HDAC6, HDAC1, and HDAC8, respectively). Nexturastat A was found to be capable of increasing acetylated α-tubulin levels and it inhibited the growth of B16 melanoma cells, albeit with lower potency than LBH 589 (Axon 1548).

        產(chǎn)品資料
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