SOS1-IN-28
SOS1-IN-28 is an orally active, blood-brain barrier permeable SOS1 inhibitor with an IC50 value of 0.11 μM. SOS1-IN-28 disrupts the SOS1: KRAS protein-protein interaction, with an IC50 of 0.29 μM for the KRAS-RAF interaction. SOS1-IN-28 blocks GTP loading of KRAS, inhibits RAS-MAPK pathway activity, and reduces cancer cell proliferation. SOS1-IN-28 can be used for the research of KRASG12C-mutant lung cancer.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 分子式: C16H14F4N4O2
- 分子量:370.30
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
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SOS1 0.11 μM (IC50) |
SOS1-IN-28 (Compound 27) (0.03 nM-30 μM; 6 days) inhibits the proliferation of NCI-H358 SOS2-/- cell spheroids in a 3D assay with a GI50 of 0.33 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Nude male mice (Envigo)[1]
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Dosage:100 mg/kg
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Administration:p.o.; single dose
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Result:Produced deeper, more sustained suppression of DUSP6 mRNA and phosphorylated ERK (pERK) at 4 h, 8 h, and 16 h compared to KRASG12C inhibitor alone.
Reduced DUSP6 mRNA expression.
Reduced pERK protein levels statistically significantly relative to vehicle control at all three time points.
Maintained unbound plasma concentrations above its biochemical and cellular proliferation IC50 for up to 16 h.
化学情報
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分子量 370.30
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分子式 C16H14F4N4O2
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SMILES
FC1=C(C(F)(F)F)C=CC=C1[C@@H](C)NC(C2=CC=NC(C(NC)=O)=N2)=O
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)