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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
1 mg/5 mg/10 mg/25 mg
| 规格: | 1 mg | 产品价格: | ¥623.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥1700.0 |
| 规格: | 10 mg | 产品价格: | ¥2700.0 |
| 规格: | 25 mg | 产品价格: | ¥4600.0 |
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JNJ-38877618
CAS No. : 943540-74-7
MCE 国际站:JNJ-38877618
产品活性:JNJ-38877618是一种有效的,高选择性的,口服可用的 (Met) 激酶抑制剂,对于野生型和突变体的 IC50 值分别为2和3 nM。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:c-Met/HGFR
In Vitro: OMO-1 (formerly JNJ-38877618), is a potent, highly selective, orally bioavailable Met kinase inhibitor with nM binding affinity (Kd=1.4 nM) and enzyme inhibitory activity against wt and M1268T mutant Met (2 and 3 nM IC50). Met inhibitory effects are assessed in proliferation, colony formation and motility assays. JNJ-38877618 displays nM potency against Met Ampl/mutant and therapy resistant models.
In Vivo: JNJ-38877618 induces complete inhibition of tumor growth in 3 models: the SNU5 Met amp gastric, U87-MG HGF autocrine glioblastoma and Hs746T Met exon 14 skipping mutant gastric cancer. JNJ-38877618 induces regression of large Met amplified EBC-1 SqNSCLC where JNJ-38877618 leads to dose- and time-dependent inhibition of Met kinase activation, with the duration of target shut down considerably exceeding plasma exposure times. Combination treatments are well tolerated and improved EGFR targeted therapy.
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