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    首頁(yè) > 產(chǎn)品中心 > 生化試劑 > 小分子化合物 > abs47027963CL-387785 194423-06-8

    CL-387785 194423-06-8

    簡(jiǎn)要描述:CL-387785 194423-06-8
    CL-387785(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to overcome resistance caused by the T790M mutation on a functional level.

    • 產(chǎn)品型號(hào):abs47027963
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時(shí)間:2026-01-09
    • 訪  問(wèn)  量:744

    詳細(xì)介紹

    品牌absinCAS194423-06-8
    分子式C18H13BrN4O純度98%
    分子量381.23貨號(hào)abs47027963
    規(guī)格10mg供貨周期現(xiàn)貨
    主要用途able to overcome resistance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

    CL-387785  194423-06-8

    產(chǎn)品描述
    描述
    CL-387785(EKI785; WAY-EKI 785) is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to overcome resistance caused by the T790M mutation on a functional level.
    純度
    98%
    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
    EKI-785; WAY-EKI 785
    外觀
    Off-white to yellow solid
    可溶性/溶解性
    DMSO : 13.67 mg/mL (35.86 mM)
    生物活性
    靶點(diǎn)
    EGFR
    In vitro(體外研究)
    CL-387785 blocks EGF-stimulated autoposphorylation of the receptor in cells (IC50, 5 nM), In cell lines that overexpress EGF-R or c-erbB-2, CL-387785 inhibits cell proliferation (IC50, 31 nM) primarily in a cytostatic manner.
    In vivo(體內(nèi)研究)
    In nude mice overexpressed EGF-R, CL-387785 (80 mg/kg/day, p.o.) profoundly blocks the growth of tumor. In murine models of autosomal recessive polycystic kidney disease (ARPKD), treatment of Balb/c-bpk/bpk (BPK) mice with CL-387785 (90 mg/kg, i.p.) results in a marked reduction of collecting tubule cystic lesions, improved renal function, decreased biliary epithelial abnormalities, and prolonged life span. Doses of CL-387785 as low as 25 mg/kg reduces the growth of HCA-7-induced xenograft tumor, and a dose of 100 mg/kg prevents tumor growth entirely. Dose of 50 mg/kg CL-387785 is effective at reducing the growth of HCT-116-induced xenograft tumor.
    研究領(lǐng)域
    研究領(lǐng)域
    CancerGrowth factorsEGF
    CancerOncoproteins/suppressorsOncoproteinsGrowth factor receptors
    CancerSignal transductionProtein phosphorylationTyrosine kinasesReceptor tyrosine kinases
    CancerTumor biomarkersReceptors
    Cell CycleCell differentiation
    MicrobiologyOrganismVirusDNA VirusssRNA positive strand virusSARS Coronavirus
    NeuroscienceDevelopment
    NeuroscienceProcesses
    Signal TransductionGrowth Factors/HormonesEGF
    Signal TransductionProtein PhosphorylationTyrosine KinasesReceptor Tyrosine Kinases
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    CL-387785  194423-06-8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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