目錄:MedChemExpress LLC>>信號通路>> Adagrasib | MedChemExpress (MCE)
CAS | 2326521-71-3 | 純度 | 99.93% |
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分子量 | 604.12 | 分子式 | C??H??ClFN?O? |
供貨周期 | 現貨 | 規(guī)格 | 10 mM * 1 mL |
貨號 | HY-130149 | 應用領域 | 醫(yī)療衛(wèi)生,化工,生物產業(yè),制藥 |
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CAS No. : 2326521-71-3
MCE 國際站:Adagrasib
產品活性:Adagrasib (MRTX849) 是一種有效,口服可用,突變選擇性的 KRAS G12C 共價抑制劑,具有潛在抗腫瘤活性的。Adagrasib 在半胱氨酸 12 殘基處與 KRAS G12C 共價結合,將蛋白鎖定在非活性的 GDP 結合構象中,并抑制 KRAS 依賴性信號轉導。
研究領域:GPCR/G Protein
作用靶點:Ras
In Vitro: Adagrasib (MRTX849) (0.1-10000 nM; 3-day/2D conditions; 12-day/3D conditions) potently inhibits cell growth in the vast majority of KRAS G12C-mutant cell lines with IC50s ranging between 10 and 973 nM in the 2D format and between 0.2 and 1042 nM in the 3D format.
Adagrasib (0.24-1000 nM; 24 hours) inhibits KRAS-dependent signaling targets including ERK1/2 phosphorylation (Thr202/Tyr204 ERK1; pERK), S6 phosphorylation (RSK-dependent Ser235/236; pS6) and expression of the ERK-regulated DUSP6.
In Vivo: Adagrasib (1-100 mg/kg; i.g.; daily until day 16) demonstrates dose-dependent anti-tumor efficacy over a well-tolerated dose range, and the maximally efficacious dose of MRTX849 is between 30-100 mg/kg/day.
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