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S84543

TANDUTINIB

源葉(MedMol) 99%
  • 英文名:
  • TANDUTINIB
  • 別名:
  • N,BETA,BETA-三甲基-L-苯基丙氨?;?N-[(1S,2E)-3-羧基-1-(1-甲基乙基)-2-丁烯基]-N,3-二甲基-L-纈氨酰胺;N,beta,beta-Trimethyl-L-phenylalanyl-N-[(1S,2E)-3-carboxy-1-(1-methylethyl)-2-butenyl]-N,3-dimethyl-L-valinamide;Taltobulin;Ht
  • CAS號(hào):
  • 228266-40-8
  • 分子式:
  • C27H31Br2ClN4O2
  • 分子量:
  • 473.65
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫(kù)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) S84543-5mg 99% ¥1840.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車
源葉(MedMol) S84543-10mg 99% ¥3400.00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)

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  • 提示:詳情請(qǐng)下載說(shuō)明書。
  • 產(chǎn)品描述: Taltobulin (HTI-286), a synthetic analogue of the tripeptide hemiasterlin, is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Taltobulin inhibits the polymerization of purified tubulin, disrupts microtubule organization in cells, and induces mitotic arrest, as well as apoptosis
  • 靶點(diǎn): Traditional Cytotoxic Agents;MicrotubuleAssociated
  • 體內(nèi)研究:
    Taltobulin (HTI-286; 1.6 mg/kg i.v.) inhibits the growth of human tumor xenografts (e.g., HCT-15, DLD-1, MX-1W, and KB-8-5) in athymic nu/nu female mice. Taltobulin (HTI-286; 3 mg/kg; p.o. gavage) inhibits growth by 97.3 % and 82% in athymic nu/nu female mice with Lox melanoma xenografts and KB-3-1 epidermoid xenograft model, respectively Animal Model: Athymic nu/nu female mice with Lox melanoma model (5-6 weeks of age) Dosage: 1.6 mg/kg Administration: Administered i.v.;for 35 days Result: Growth of Lox tumors was inhibited by 96-98% on day 12 compared with vehicle-treated controls.Growth of KB-8-5 tumors was inhibited by 84% on day 14 compared with vehicle-treated controls.Growth of MX-1W tumors was inhibited by 97% compared with vehicle-treated controls.Growth of DLD-1 and HCT-15 tumors was inhibited by 80 and 66%, respectively.
  • 參考文獻(xiàn):
    1. Loganzo F, et al. HTI-286, a synthetic analogue of the tripeptide hemiasterlin, is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Cancer Res. 2003 Apr 15;63(8):1838-45.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.111 ml 10.556 ml 21.113 ml
    5 mM 0.422 ml 2.111 ml 4.223 ml
    10 mM 0.211 ml 1.056 ml 2.111 ml
    50 mM 0.042 ml 0.211 ml 0.422 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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