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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-Ras-INCB159020
INCB159020

Chemical Structure : INCB159020

CAS No.: 2923669-20-7

INCB159020 (INCB 159020)

货号: PC-23776Not For Human Use, Lab Use Only.

INCB159020 is a potent, selective KRAS G12D inhibitor with SPR binding Kd of 22 nM, IC50 of 33 nM in HTRF pERK cell assays.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

INCB159020 is a potent, selective KRAS G12D inhibitor with SPR binding Kd of 22 nM, IC50 of 33 nM in HTRF pERK cell assays.
INCB159020 shows significant selectivity over inhibition of wild-type KRAS, in binding (50× vs binding to KRAS WT), a pERK setting (80 fold selectivity vs a wild-type H838 line) and in a viability setting (28 fold vs a H838 wild-type line).
INCB159020 (30, 100 and 300 mg/kg, oral) dose dependently inhibits pERK levels in HPAC mouse model.

物理化学性质&存储条件

分子量 664.18
分子式 C37H35ClFN7O2
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

3-(1-((1R,4R,5S)-2-Azabicyclo[2.1.1]hexan-5-yl)-7-(3-chloro-2-methylphenyl)-6-fluoro-4-(5-methylpyrazin-2-yl)-2-((R)-1-(3-oxomorpholino)ethyl)-1H-pyrrolo[3,2-c]quinolin-8-yl)propanenitrile

参考文献

1. Ye Q, et al. J Med Chem. 2025 Jan 8. doi: 10.1021/acs.jmedchem.4c02662.

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