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PLX-4720

    99%

PLX-4720

源葉(MedMol)
S81102
918505-84-7
C17H14ClF2N3O3S
413.83
N-(3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonamide
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫存(上海) 北京 武漢 南京 購(gòu)買數(shù)量
源葉(MedMol) S81102-5mg 99% ¥255.00元 7 - - -
源葉(MedMol) S81102-10mg 99% ¥425.00元 6 - - -
源葉(MedMol) S81102-25mg 99% ¥680.00元 8 - - -
源葉(MedMol) S81102-50mg 99% ¥935.00元 8 - - -
源葉(MedMol) S81102-100mg 99% ¥1700.00元 6 - - -
源葉(MedMol) S81102-200mg 99% ¥2975.00元 5 - - -
源葉(MedMol) S81102-500mg 99% ¥4930.00元 5 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

PLX-4720 is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM in a cell-free assay, equally potent to c-Raf-1(Y340D and Y341D mutations), and 10-fold selectivity for B-RafV600E than wild-type B-Raf.
產(chǎn)品描述: PLX-4720 is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM in a cell-free assay, equally potent to c-Raf-1(Y340D and Y341D mutations), and 10-fold selectivity for B-RafV600E than wild-type B-Raf.
靶點(diǎn): B-RafV600E:13 nM (IC50);B-Raf:160 nM (IC50);BRK:130 nM (IC50);FRK:1300 nM (IC50);Csk:1500 nM (IC50);Src:1700 nM (IC50);FAK:1700 nM (IC50);FGFR:1900 nM (IC50);KDR:2300 nM (IC50);HGK:2800 nM (IC50);CSF1R:3300 nM (IC50);Aurora A:3400 nM (IC50);Raf
體內(nèi)研究: Oral administration of PLX-4720 at 20 mg/kg/day induces significant tumor growth delays and regressions in B-RafV600E-dependent COLO205 tumor xenografts, without obvious adverse effects in mice even at dose of 1 g/kg. PLX-4720 at 100 mg/kg twice daily almost completely eliminates the 1205Lu xenografts bearing B-RafV600E, while has no activity against C8161 xenografts bearing wild-type B-Raf. The anti-tumor effects of PLX-4720 correlate with the blockade of MAPK pathway in those cells harboring the V600E mutation. PLX-4720 treatment at 30 mg/kg/day significant inhibits the tumor growth of 8505c xenografts by >90%, and dramatically decreases distant lung metastases
參考文獻(xiàn): 1. Tsai J, et al. Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc Natl Acad Sci U S A, 2008, 105(8), 3041-3046. 2. Paraiso KH, et al. PTEN loss confers BRAF inhibitor resistance to melanoma cells through the suppression of BIM expression. Cancer Res, 2011, 71(7), 2750-2760. 3. Nucera C, et al. B-Raf(V600E) and thrombospondin-1 promote thyroid cancer progression. Proc Natl Acad Sci U S A, 2010, 107(23), 10649-10654. 4. Rizzolio S, et al. Neuropilin-1 upregulation elicits adaptive resistance to oncogene-targeted therapies. J Clin Invest. 2018 Aug 31;128(9):3976-3990.
溶解性: Soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.416 ml 12.082 ml 24.165 ml
5 mM 0.483 ml 2.416 ml 4.833 ml
10 mM 0.242 ml 1.208 ml 2.416 ml
50 mM 0.048 ml 0.242 ml 0.483 ml
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摩爾濃度計(jì)算器

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