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        產(chǎn)品名稱 STK16-IN-1
        產(chǎn)品貨號(hào) Axon 2743 CAS [1223001-53-3] MF C17H12FN3OMW 293.30 Purity: 99% Soluble in DMSO Description STK16-IN-1 is a highly selective ATP-competitive inhibitor which exhibits potent inhibitory activity against STK16 kinase (IC50 value of 0.295 μM). In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics results in a slight potentiation of the antiproliferative effects of the chemotherapeutics. References Certificates Categories Extra info F Liu et al. Discovery of a Highly Selective STK16 Kinase Inhibitor. ACS Chem Biol. 2016 Jun 17;11(6):1537-43. Certificate of Analysis Material Safety Data Sheet Cell Signaling & Oncology EC 2.7.10.2 STK16 ATP-competitive STK16 inhibitor Chemical name 1-(4-Fluoro-3-methylphenyl)-1H-pyrrolo[2,3-h][1,6]naphthyridin-2(7H)-one Parent CAS No. [1223001-53-3] Order Size Unit Price Stock 10 mg €125.00 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

        STK16-IN-1

        Based on 1 reference(s) in Google Scholar 8 10 1

        Axon 2743

        CAS [1223001-53-3]

        MF C17H12FN3O
        MW 293.30

        • Purity: 99%
        • Soluble in DMSO

        STK16-IN-1

        Description

        STK16-IN-1 is a highly selective ATP-competitive inhibitor which exhibits potent inhibitory activity against STK16 kinase (IC50 value of 0.295 μM). In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics results in a slight potentiation of the antiproliferative effects of the chemotherapeutics.
        產(chǎn)品資料
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