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Adagrasib

CAS No. : 2326521-71-3

MCE 國(guó)際站：Adagrasib

產(chǎn)品活性：Adagrasib (MRTX849) 是一種有效，口服可用，突變選擇性的 KRAS G12C 共價(jià)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(jià)結(jié)合，將蛋白鎖定在非活性的 GDP 結(jié)合構(gòu)象中，并抑制 KRAS 依賴性信號(hào)轉(zhuǎn)導(dǎo)。

研究領(lǐng)域：GPCR/G Protein

作用靶點(diǎn)：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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