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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-Ras-MK-1084
MK-1084

Chemical Structure : MK-1084

CAS No.: 2641216-67-1

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MK-1084 (MK1084)

货号: PC-22632Not For Human Use, Lab Use Only.

MK-1084 is a potent, orally bioavailable and low-dose KRAS G12C covalent inhibitor with IC50 of 1.2 nM in in vitro guanine nucleotide exchange assay, and 9 nM in cell-based phospho-ERK1/2 assay with H358 cell line.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

MK-1084 is a potent, orally bioavailable and low-dose KRAS G12C covalent inhibitor with IC50 of 1.2 nM in in vitro guanine nucleotide exchange assay, and 9 nM in cell-based phospho-ERK1/2 assay with H358 cell line.
MK-1084 30 mg/kg QD dosing demonstrated excellent efficacy in patient-derived xenograft models, LU2512 and LU2529.

物理化学性质&存储条件

分子量 637.08
分子式 C32H31ClF2N6O4
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

1,18-Etheno-4H-pyrido[4,3-e]pyrimido[1,6-g][1,4,7,9]benzodioxadiazacyclododecin-4-one, 20-chloro-2-[(2S,5R)-2,5-dimethyl-4-(1-oxo-2-propen-1-yl)-1-piperazinyl]-14,17-difluoro-11,12-dihydro-6-(1-methylethyl)-, (5S,17aR)-

参考文献

1. Ma X, et al. J Med Chem. 2024 Jun 26. doi: 10.1021/acs.jmedchem.4c00572.

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