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bgb 283

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  • 抑制剂&激动剂
    4
    TargetMol | Inhibitors_Agonists
  • Lifirafenib
    BGB-283, Beigene-283
    T222721446090-79-4
    Lifirafenib (Beigene-283) 是新型高效的Raf 激酶和EGFR 抑制剂,对重组BRafV600E 和EGFR 的IC50值分别为 23 和 29 nM。
    • ¥ 237
    现货
    规格
    数量
  • Ticalopride
    T69984202590-69-0In house
    Ticalopride是一种5-HT3 receptor激动剂,可用于治疗消化系统疾病、口颌疾病、耳鼻咽喉疾病,可用于研究神经性贪食症、胃食管反流和肠易激综合征。
    • ¥ 360
    现货
    规格
    数量
    TargetMol | Inhibitor Sale
  • Lifirafenib maleate
    BGB-283 maleate
    T868101854985-74-2
    Lifirafenib (BGB-283) maleate 是一种高效的Raf激酶和EGFR抑制剂,对重组BRafV600E和EGFR的IC50值分别为23 nM和29 nM。
    • 待询
    10-14周
    规格
    数量
  • Lifirafenib HCl
    T699852025320-97-0
    Lifirafenib, also known as Beigene-283, is a Novel potent and selective RAF Kinase and EGFR inhibitor. BGB-283-displays Potent Antitumor Activity in B-RAF Mutated Colorectal Cancers. In vitro, BGB-283 potently inhibits B-RAFV600E-activated ERK phosphorylation and cell proliferation. It demonstrates selective cytotoxicity and preferentially inhibits proliferation of cancer cells harbouring B-RAFV600E and EGFR mutation amplification. In B-RAFV600E CRC cell lines, BGB-283 effectively inhibits the reactivation of EGFR and EGFR-mediated cell proliferation. In vivo, BGB-283 treatment leads to dose-dependent tumor growth inhibition accompanied by partial and complete tumor regressions in both cell-line derived and primary human colorectal tumor xenografts bearing B-RAFV600E mutation. BGB-283 as a potent antitumor drug candidate with clinical potential for treating CRC harbouring B-RAFV600E mutation.
    • ¥ 13900
    1-2周
    规格
    数量