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S80974

Palbociclib isethionate

源葉(MedMol) 99%
  • 英文名:
  • Palbociclib isethionate
  • 別名:
  • CAS號:
  • 827022-33-3
  • 分子式:
  • C24H29N7O2·C2H6O4S
  • 分子量:
  • 573.66
  • MDL:
  • MFCD22666589
  • 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(jì)量單位 加入購物車...
源葉(MedMol) S80974-2mg 99% ¥168.00元 >10 - - - EA 加入購物車
源葉(MedMol) S80974-5mg 99% ¥240.00元 7 - - - EA 加入購物車
源葉(MedMol) S80974-25mg 99% ¥280.00元 7 - - - EA 加入購物車
源葉(MedMol) S80974-100mg 99% ¥784.00元 1 - 5 - EA 加入購物車
源葉(MedMol) S80974-200mg 99% ¥1280.00元 5 - - - EA 加入購物車
源葉(MedMol) S80974-500mg 99% ¥2000.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S80974-1g 99% ¥3500.00元 1 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻(xiàn)(1篇)

質(zhì)檢證書(COA)

摩爾濃度計(jì)算器

相關(guān)產(chǎn)品

  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Palbociclib (PD 0332991) isethionate is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively. Palbociclib isethionate has potent anti-proliferative activity and induces cell cycle arrest in cancer cells, which can be used in the research of HR-positive and HER2-negative breast cancer and hepatocellular carcinoma
  • 靶點(diǎn): Cdk4/cyclin D3:9 nM (IC50);Cdk4/cyclin D1:11 nM (IC50);Cdk6/cyclin D2:16 nM (IC50);DYRK1A:2000 nM (IC50);MAPK:8000 nM (IC50);CDK
  • 體內(nèi)研究:
    Palbociclib isethionate (oral adminstration, 75 or 150 mg/kg, daily for 14 days) produces rapid tumor regressions and delays tumor growth. Palbociclib isethionate (oral adminstration, 90 mg/kg, daily for 12 days) reduces Treg numbers and the Treg:CD8 ratio in the spleen and lymph nodes in tumor-free mice, demonstrating the tumor-independent effects. Palbociclib isethionate (oral administration, 100 mg/kg, daily for 1 week) has potent antitumour effects in genetically engineered mosaic mouse model of liver cancer.
  • 參考文獻(xiàn):
    1. Fry DW, et al. Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts. Mol Cancer Ther. 2004 Nov;3(11):1427-38. 2. Goel S, et al. CDK4/6 inhibition triggers anti-tumour immunity. Nature. 2017 Aug 24;548(7668):471-475. 3. Richard S Finn, et al. PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res. 2009;11(5):R77. 4. Bollard J, et al. Palbociclib (PD-0332991), a selective CDK4/6 inhibitor, restricts tumour growth in preclinical models of hepatocellular carcinoma. Gut. 2017 Jul;66(7):1286-1296.
  • 溶解性: H2O  :  50  mg/mL  (87.16  mM;  Need  ultrasonic)    DMSO  :  10  mg/mL  (17.43  mM;  Need  ultrasonic)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.743 ml 8.716 ml 17.432 ml
    5 mM 0.349 ml 1.743 ml 3.486 ml
    10 mM 0.174 ml 0.872 ml 1.743 ml
    50 mM 0.035 ml 0.174 ml 0.349 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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