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S80570

Tasquinimod

源葉(MedMol) 99%
  • 英文名:
  • Tasquinimod
  • 別名:
  • CAS號:
  • 254964-60-8
  • 分子式:
  • C20H17F3N2O4
  • 分子量:
  • 406.36
  • 核磁/質(zhì)譜:
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S80570-2mg 99% ¥465.00元 >10 - - - EA 加入購物車
源葉(MedMol) S80570-5mg 99% ¥670.00元 >10 - - - EA 加入購物車
源葉(MedMol) S80570-10mg 99% ¥960.00元 >10 - - - EA 加入購物車
源葉(MedMol) S80570-25mg 99% ¥1590.00元 10 - - - EA 加入購物車
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參考文獻

質(zhì)檢證書(COA)

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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Tasquinimod is an oral antiangiogenic agent, which has the potential for castration-resistant prostate cancer treatment. Tasquinimod binds to the regulatory Zn2+ binding domain of HDAC4 with Kd of 10-30 nM. Tasquinimod also is a S100A9 inhibitor
  • 靶點: HDAC4:10-30 nM (Kd);HDAC
  • 體內(nèi)研究:
    The bioavailability and oral absorption of Tasquinimod is excellent when adult male mice (i.e., C57Bl/6J, or athymic nude mice) are given 0.1-30 mg/kg (i.e., 0.2-74 μmoles/kg) via gavage or the drinking water. The potency of Tasquinimod expressed as the daily oral dose of Tasquinimod which inhibits cancer growth by 50% ranges from 0.1-1.0 mg/kg/d (i.e., 0.24-2.40 μmoles/kg/day) against a series (n>5) of human prostate cancer xenografts in immune-deficient mice. Tasquinimod at a chronic dose of 5 mg/kg/day via the drinking water produces > 80% inhibition (p<0.05) of TRAMP-C2 mouse prostate cancer growth in immune-competent syngeneic mice. Nude mice carrying subcutaneous LNCaP tumors are treated with Tasquinimod for 3 weeks. Exposure to Tasquinimod at 1 mg/kg/day and 10 mg/kg/day started on day 7 after inoculation. There is a statistically significant dose dependent reduction in tumor weight both at 1 mg/kg/day and 10 mg/kg/day compare to the untreated control group 28 days after inoculation (p<0.001), illustrating the anti-tumor effect of Tasquinimod
  • 參考文獻:
    1. Isaacs JT, et al. Tasquinimod Is an Allosteric Modulator of HDAC4 survival signaling within the compromised cancer microenvironment. Cancer Res. 2013 Feb 15;73(4):1386-99. 2. Isaacs JT, et al. Anti-cancer potency of tasquinimod is enhanced via albumin-binding facilitating increased uptake in the tumor microenvironment. Oncotarget. 2014 Sep 30;5(18):8093-106. 3. Olsson A, et al. Tasquinimod (ABR-215050), a quinoline-3-carboxamide anti-angiogenic agent, modulates the expression of thrombospondin-1 in human prostate tumors. Mol Cancer. 2010 May 17;9:107.
  • 溶解性: DMSO  :  ≥  42  mg/mL  (103.36  mM)    H2O  :  <  0.1  mg/mL  (ultrasonic;warming;heat  to  60°C)  (insoluble)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.461 ml 12.304 ml 24.609 ml
    5 mM 0.492 ml 2.461 ml 4.922 ml
    10 mM 0.246 ml 1.23 ml 2.461 ml
    50 mM 0.049 ml 0.246 ml 0.492 ml
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