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S80501

Tipifarnib

源葉(MedMol) 98%
  • 英文名:
  • Tipifarnib
  • 別名:
  • R115777;(R)-6-(amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methylquinolin-2(1H)-one
  • CAS號(hào):
  • 192185-72-1
  • 分子式:
  • C27H22Cl2N4O
  • 分子量:
  • 489.4
  • 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 加入購物車...
源葉(MedMol) S80501-2mg 98% ¥240.00元 8 - - - EA 加入購物車
源葉(MedMol) S80501-5mg 98% ¥380.00元 3 - - - EA 加入購物車
源葉(MedMol) S80501-10mg 98% ¥610.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S80501-50mg 98% ¥1960.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S80501-100mg 98% ¥3100.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(COA)

摩爾濃度計(jì)算器

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  • 提示:詳情請(qǐng)下載說明書。
  • 產(chǎn)品描述: Tipifarnib (IND 58359) binds to and inhibits farnesyltransferase (FTase) with an IC50 of 0.86 nM. Antineoplastic activity
  • 靶點(diǎn): IC50: 0.86 nM (FTase);Transferase
  • 體內(nèi)研究:
    Combined therapy with ICI 47699 and Tipifarnib (50 mg/kg, p.o.) produces greater tumor growth inhibition when compared with either drug alone. E2 deprivation and Tipifarnib in combination results in greater growth inhibition than either E2 deprivation or Tipifarnib alone. The combination of ICI 47699 and Tipifarnib results in significantly lower Ki-67 compared with either ICI 47699 or Tipifarnib alone. Tipifarnib alone also reduces the CTI compared with control. The combination of ICI 47699 and Tipifarnib or Tipifarnib coupled with E2 withdrawal is most effective at lowering the CTI (0.8 and 0.7, respectively), which may account for the decrease in tumor volume
  • 參考文獻(xiàn):
    1. Devendra S Puntambekar, et al. Inhibition of farnesyltransferase: a rational approach to treat cancer? J Enzyme Inhib Med Chem. 2007 Apr;22(2):127-40. 2. Martin LA, et al. The farnesyltransferase inhibitor R115777 (tipifarnib) in combination with ICI 47699 acts synergistically to inhibit MCF-7 breast cancer cell proliferation and cell cycle progression in vitro and in vivo. Mol Cancer Ther. 2007 Sep;6(9):2 3. End DW, et al. Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro. Cancer Res. 2001 Jan 1;61(1):131-7 4. Amrita Datta, et al. High-throughput screening identified selective inhibitors of exosome biogenesis and secretion: A drug repurposing strategy for advanced cancer. Sci Rep. 2018 May 25;8(1):8161.
  • 溶解性: DMSO  :  100  mg/mL  (204.33  mM;  Need  ultrasonic)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.043 ml 10.217 ml 20.433 ml
    5 mM 0.409 ml 2.043 ml 4.087 ml
    10 mM 0.204 ml 1.022 ml 2.043 ml
    50 mM 0.041 ml 0.204 ml 0.409 ml
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