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首页-小分子抑制剂&激动剂-Tyrosine Kinase-c-Met (HGFR)-PLB-1001
PLB-1001

Chemical Structure : PLB-1001

CAS No.: 1440964-89-5

PLB-1001 (Bozitinib, Vebreltinib, PLB1001, CBI-3103, CBT-101)

货号: PC-35732Not For Human Use, Lab Use Only.

PLB-1001 (Bozitinib, PLB1001, CBI-3103, CBT-101) is a potent, highly selective, ATP-competitive, BBB-permeable MET kinase inhibitor, potently inhibits MET activity by 95.1% at 2 uM.

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纯度 & COA & 质检文件 纯度: 98.25% (HPLC) Select Batch:

生物&药学活性

PLB-1001 (Bozitinib, Vebreltinib, PLB1001, CBI-3103, CBT-101) is a potent, highly selective, ATP-competitive, BBB-permeable MET kinase inhibitor, potently inhibits MET activity by 95.1% at 2 uM.
Similar with crizotinib, PLB-1001 inhibited the phosphorylation of MET and STAT3, indicating a robust inhibitory effect of PLB-1001 on MET and its downstream signaling pathways.
PLB-1001 demonstrates remarkable potency in selectively inhibiting MET-altered tumor cells (METex14) in preclinical models.
PLB-1001 also exhibits clinical potential for precisely treating gliomas.

物理化学性质&存储条件

分子量 424.391
分子式 C20H15F3N8
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

6-(1-cyclopropyl-1H-pyrazol-4-yl)-3-(difluoro(6-fluoro-2-methyl-2H-indazol-5-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazine

参考文献

1. Hu H, et al. Cell. 2018 Oct 12. pii: S0092-8674(18)31250-9.

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