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S83728

Salirasib

源葉(MedMol) 98%
  • 英文名:
  • Salirasib
  • 別名:
  • 2-[[(2E,6E)-3,7,11-三甲基-2,6,10-十二烷三烯-1-基]硫代]苯甲酸;Farnesyl thiosalicylate; Farnesyl thiosalicylic acid; Lopac-F-8175; Salirasib; FTS; S-Farnesylthiosalicylic acid; 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,1
  • CAS號(hào):
  • 162520-00-5
  • 分子式:
  • C22H30O2S
  • 分子量:
  • 358.54
  • 核磁/質(zhì)譜:
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 數(shù)量計(jì)量單位 加入購(gòu)物車...
源葉(MedMol) S83728-5mg 98% ¥100.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車
源葉(MedMol) S83728-10mg 98% ¥145.00元 7 - - - EA 加入購(gòu)物車
源葉(MedMol) S83728-25mg 98% ¥245.00元 1 - - - EA 加入購(gòu)物車
源葉(MedMol) S83728-50mg 98% ¥400.00元 7 - - - EA 加入購(gòu)物車
源葉(MedMol) S83728-100mg 98% ¥680.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車
源葉(MedMol) S83728-200mg 98% ¥1280.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(COA)

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  • 提示:詳情請(qǐng)下載說明書。
  • 產(chǎn)品描述: Salirasib is a Ras inhibitor that inhibits specifically both oncogenically activated Ras and growth factor receptor-mediated Ras activation, resulting in the inhibition of Ras-dependent tumor growth.
  • 靶點(diǎn): Ki: 2.6 μM (PPMTase);Autophagy;?Ras
  • 體外研究:
    Salirasib (12.5-100 μM) inhibits the proliferation of ELT3 cells in a dose-dependent manner with an average IC50 of 58.57±4.59 μM. The effects of Salirasib on the TSC2-null cells are evidently mimicked by DN-Rheb but not by DN-Ras. Salirasib reduces Rheb in TSC2-null cells and TSC2 expression rescues the cells from the inhibitory effect of Salirasib. Salirasib reduces phosphorylation of S6K but not of ERK in the TSC2-null ELT3 cells. Salirasib (50, 100, 150 μM) induces a dose- and time-dependent decrease of cell growth in HCC cells. Salirasib reduces cell proliferation through modulation of cell cycle effectors and inhibitors. Salirasib induces apoptosis in HepG2 and Hep3B cells. The growth inhibitory effect of salirasib in HCC cell lines is associated with mTOR inhibition independent of ERK or Akt activation
  • 體內(nèi)研究:
    Salirasib (40, 60 or 80 mg/kg, p.o.) significantly inhibits the tumor growth in a dose dependent manner in vivo[1]. Salirasib (5 mg/kg, i.p.) significantly decreases Ras expression in the?dy2J/dy2Jmice, and causes an increase in Ras expression which is by far much lower than the increase observed in the?dy2J/dy2J?mice. Salirasib treatment is associated with significantly inhibition of both MMP-2 and MMP-9 activities in the?dy2J/dy2J?mice[2]. Salirasib (10 mg/kg, i.p.) inhibits tumour growth in a subcutaneous xenograft mice model without weight loss
  • 參考文獻(xiàn):
    1. Makovski V, et al. Farnesylthiosalicylic acid (salirasib) inhibits Rheb in TSC2-null ELT3 cells: a potential treatment for lymphangioleiomyomatosis. Int J Cancer. 2012 Mar 15;130(6):1420-9. 2. Nevo Y, et al. Chapman J. The Ras antagonist, farnesylthiosalicylic acid (FTS), decreases fibrosis and improves muscle strength in dy/dy mouse model of muscular dystrophy. PLoS One. 2011 Mar 22;6(3):e18049. 3. Charette N, et al. Salirasib inhibits the growth of hepatocarcinoma cell lines in vitro and tumor growth in vivo through ras and mTOR inhibition. Mol Cancer. 2010 Sep 22;9:256.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.789 ml 13.945 ml 27.891 ml
    5 mM 0.558 ml 2.789 ml 5.578 ml
    10 mM 0.279 ml 1.395 ml 2.789 ml
    50 mM 0.056 ml 0.279 ml 0.558 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)


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