PLX7904

    
≥97%

PLX7904

源葉(MedMol)
S81311 一鍵復(fù)制產(chǎn)品信息
1393465-84-3
C24H22F2N6O3S
貨號(hào) 規(guī)格 價(jià)格 上海 北京 武漢 南京 購(gòu)買數(shù)量
S81311-5mg ≥97% ¥720.00 10 - - -
S81311-10mg ≥97% ¥1230.00 7 - - -
S81311-25mg ≥97% ¥2670.00 3 - - -
S81311-50mg ≥97% ¥4325.00 1 - - -
S81311-100mg ≥97% ¥7200.00 1 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(shū)(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

PLX7904, also known as PB04, is a potent and selective paradox-breaker RAF inhibitor. It is able to efficiently inhibit activation of ERK1/2 in mutant BRAF melanoma cells but does not hyperactivate ERK1/2 in mutant RAS-expressing cells.

產(chǎn)品描述: PLX7904, also known as PB04, is a potent and selective paradox-breaker RAF inhibitor. It is able to efficiently inhibit activation of ERK1/2 in mutant BRAF melanoma cells but does not hyperactivate ERK1/2 in mutant RAS-expressing cells.
靶點(diǎn): Raf
體內(nèi)研究: PLX7904 inhibits the COLO205 xenograft growth in eight mice per group
細(xì)胞實(shí)驗(yàn): Cells are treated with PB04(PLX7904) at different concentrations (0, 0.05, 0.1, 1, 5 μM) for 24 h. Cells are lysed and analyzed by Western blotting with phospho-MEK1/2, total MEK1/2, phospho-ERK1/2 and total ERK1/2 antibodies. (Only for Reference)
參考文獻(xiàn): 1. Zhang C, et al. Nature. 2015, 526(7574):583-586. 2. Le K, et al. Pigment Cell Melanoma Res. 2013, 26(4):509-517.
溶解性: Soluble  in  DMSO
保存條件: -20°C
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 0 ml 0 ml 0 ml
5 mM 0 ml 0 ml 0 ml
10 mM 0 ml 0 ml 0 ml
50 mM 0 ml 0 ml 0 ml
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參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

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摩爾濃度計(jì)算器

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