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      HMN-214 173529-46-9

      簡(jiǎn)要描述:HMN-214 173529-46-9
      HMN-214(IVX214) is a potent PLK1 inhibitor an average IC50 of 0.12 μM.

      • 產(chǎn)品型號(hào):abs47028045
      • 廠商性質(zhì):生產(chǎn)廠家
      • 更新時(shí)間:2026-01-14
      • 訪  問(wèn)  量:673

      詳細(xì)介紹

      品牌absinCAS173529-46-9
      分子式C22H20N2O5S純度99%
      分子量424.47貨號(hào)abs47028045
      規(guī)格5mg供貨周期現(xiàn)貨
      主要用途is a potent PLK1 inhibitor應(yīng)用領(lǐng)域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

      HMN-214 173529-46-9

      產(chǎn)品描述
      描述

      HMN-214(IVX214) is a potent PLK1 inhibitor an average IC50 of 0.12 μM.

      純度
      99%
      儲(chǔ)存/保存方法
      Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
      基本信息
      別名
      HMN-214,HMN214,HMN 214,IVX214
      可溶性/溶解性
      10 mM in DMSO
      生物活性
      靶點(diǎn)
      Polo-like Kinase (PLK)
      In vitro(體外研究)
      HMN-214 is a prodrug of HMN-176. HMN-176 shows potent activities against 22 human tumor cell lines, with a mean IC50s of 118 nM. HMN-176 (3-300 nM) inhibits luciferase expression driven by the MDR1 promoter in a dose dependent manner in HeLa cells. HMN-176 (30-3000 nM) also dose-dependently suppresses complex formation on the Y-box. HMN-214 (3.3 μM) enhances luciferase expression relative to vehicle control with the 1,4C-1,4Bis polymer (11-fold) and PEI (37-fold) in PC3-PSMA cells. HMN-214 (≥ 3.3 μM) significantly reduces cell proliferation, causes considerable changes in cell morphology in MB49 cells.
      In vivo(體內(nèi)研究)
      HMN-214 (33 mg/kg, p.o.) converts to HMN-176 in rats. HMN-214 has no effect on the conduction velocity and the amplitude of action potentials in the aciatic and tibial nerves. HMN-214 (20 mg/kg, p.o.) exhibits antitumor activity in mice. HMN-214 (10, 20 mg/kg, p.o.) decreases MDR1 mRNA expression in nude mice bearing KB- and KB-A.1.-derived tumors.
      參考文獻(xiàn)
      參考文獻(xiàn)
      • 1. Garland LL, et al. Clin Cancer Res. 2006 Sep 1;12(17):5182-9.

      • 2. Takagi M, et al. Invest New Drugs. 2003 Nov;21(4):387-99.

      研究領(lǐng)域
      研究領(lǐng)域
      CancerCell cycleCell division
      Cell CycleCell DivisionSpindle
      Cell CycleKinases/PhosphatasesOther
      EpigeneticsCell cycleKinases/PhosphatasesOther
      NeuroscienceProcesses
      Drug DiscoverySmall Molecule DrugLead Compound Discovery
      HMN-214 173529-46-9溫馨提示:本產(chǎn)品僅作科研實(shí)驗(yàn)使用,不支持臨床等研究

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