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PLX7904

    
10mM in DMSO

PLX7904

源叶(MedMol)
S56496 一键复制产品信息
1393465-84-3
C24H22F2N6O3S
512.53
PB04Sulfamide,N'-​[3-​[[5-​(2-​cyclopropyl-​5-​pyrimidinyl)​-​1H-​pyrrolo[2,​3-​b]​pyridin-​3-​yl]​carbonyl]​-​2,​4-​difluorophenyl]​-​N-​ethyl-​N-​methyl-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S56496-1ml促销
10mM in DMSO

¥720.00 ¥648.00

8 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Raf抑制剂;Raf Inhibitors;;InformationPLX7904 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.TargetsRafIn vitroPLX7940 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.Consistent with ERK1/2 re-activation driving the re-acquisition of malignant properties, PLX7904 promotes apoptosis and inhibits entry into S phase and anchorage-independent growth in mutant N-RAS mediated vemurafenib-resistant cells.PLX7904 is also evaluated in the human SCC cell line A431 and the human breast adenocarcinoma cell line SKBR3 as these cells achieve MAPK pathway activation by upstream signals feeding into RAS (through overexpression of epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (HER2), respectively).In vivoPLX7904 inhibits the COLO205 xenograft growth in eight mice per group.Cell Research(from reference)Cell lines:WM793, WM115, WM9, WM278, WM1346, WM1366, WM1361A, Sbcl2, 1205Lu, A375, SK-MEL 24, SKMEL-2, and SK-MEL 207 cells Concentrations:0, 0.5, 1, 5 μM Incubation Time:24 h 
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.951 ml 9.756 ml 19.511 ml
5 mM 0.39 ml 1.951 ml 3.902 ml
10 mM 0.195 ml 0.976 ml 1.951 ml
50 mM 0.039 ml 0.195 ml 0.39 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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