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        產(chǎn)品名稱 NVP-BGT226 - BGT 226
        產(chǎn)品貨號 Axon 2029 CAS [1245537-68-1] MF C28H25F3N6O2.C4H4O4MW 650.60 Purity: 99% Soluble in DMSO Description Orally active dual PI3K/mTOR inhibitor; induces cell cycle arrest and regulates survivin gene expression in human pancreatic cancer cell lines; inhibits growth in common myeloma cell lines and primary myeloma cells at nanomolar concentrations in a time-dependent and dose-dependent manner References Certificates Categories Extra info KY Chang et al. Novel phosphoinositide 3-kinase/mTOR dual inhibitor, NVP-BGT226, displays potent growth-inhibitory activity against human head and neck cancer cells in vitro and in vivo. Clin. Cancer Res. 2011, 17(22), 7116-26. ? W Glienke et al. The dual PI3K/mTOR inhibitor NVP-BGT226 induces cell cycle arrest and regulates Survivin gene expression in human pancreatic cancer cell lines. Tumour Biol. 2012, 33(3), 757-765.? ? P Baumann et al. Simultaneous targeting of PI3K and mTOR with NVP-BGT226 is highly effective in multiple myeloma. Anticancer Drugs. 2012, 23(1), 131-138. Certificate of Analysis Material Safety Data Sheet Apoptosis Cell Cycle Regulation Cell Signaling & Oncology PI3K mTOR PI3K-Akt-mTOR EC 2.7.11.1 Orally active dual PI3K/mTOR inhibitor Chemical name 8-(6-methoxypyridin-3-yl)-3-methyl-1-(4-(piperazin-1-yl)-3-(trifluoromethyl)phenyl)-1H-imidazo[4,5-c]quinolin-2(3H)-one maleate Parent CAS No. [915020-55-2] Order Size Unit Price Stock 5 mg €120.00 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

        NVP-BGT226 - BGT 226

        Based on 8 reference(s) in Google Scholar 9 10 8

        Axon 2029

        CAS [1245537-68-1]

        MF C28H25F3N6O2.C4H4O4
        MW 650.60

        • Purity: 99%
        • Soluble in DMSO

        NVP-BGT226

        Description

        Orally active dual PI3K/mTOR inhibitor; induces cell cycle arrest and regulates survivin gene expression in human pancreatic cancer cell lines; inhibits growth in common myeloma cell lines and primary myeloma cells at nanomolar concentrations in a time-dependent and dose-dependent manner
        產(chǎn)品資料
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