mIDH1-IN-2
mIDH1-IN-2 is a brain-penetrant isocitrate dehydrogenase 1 (IDH1) inhibitor. mIDH1-IN-2 shows subnanomolar potency against IDH1 R132H and R132C (IC50 = 80.0 and 58.0 nM) and minimal activity against wt-IDH1/2. mIDH1-IN-2 also inhibits PDK1 (IC50 = 0.61 μM) and reduces PDH phosphorylation dose-dependently. mIDH1-IN-2 can inhibit cells proliferation, induces S phase arrest and promotes apoptosis. mIDH1-IN-2 can be used for the research of cancer, such as glioma.
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- 分子式: C18H15Br2NO4S
- 分子量:501.19
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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R132H IDH1 80 nM (IC50) |
R132C IDH1 58 nM (IC50) |
mIDH1-IN-2 (Compound 27j) inhibits HT1080 and U87-MG cells proliferation all profile with EC50 values of 121.1 nM and 69.0 nM, respectively[1].
mIDH1-IN-2 (1-5 μM, 24-48 h) induces S phase arrest and apoptosis in U87-MG IDH1 R132H cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:U87-MG IDH1 R132H cells
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Concentration:1, 2 and 5 μM
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Incubation Time:24 and 48 h
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Result:Increased the proportion of apoptotic cells.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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分子量 501.19
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分子式 C18H15Br2NO4S
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SMILES
O=C(C1=CC=C(SC2=CC=CC(OC3CCC3)=C2)C([N+]([O-])=O)=C1)C(Br)Br
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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)
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