LM11
LM11 is an inhibitor of transglutaminase 2 (TG2) with an activity of killing glioblastoma cells by maintaining TG2 in a cytotoxic conformational state.
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- 分子式: C26H18Cl2N4O5
- 分子量:537.35
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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
LM11 (0.1-100 μM, 6 h) inhibits MDA-MB-231 cell migration in a dose-dependent fashion at stimulation with EGF.
LM11 (100 μM, 16 h) inhibits MDA-MB-231 cell viability with a 60% death rate.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:MDA-MB-231
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Concentration:0.1, 1, 10, 100 μM
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Incubation Time:6 h
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Result:Inhibited cell migration at 10 uM of stimulation with EGF.
Inhibited cell viability at 100 uM after 16 h.
化学情報
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分子量 537.35
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分子式 C26H18Cl2N4O5
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SMILES
O=C1NC(N(C(/C1=C/NC2=CC(CN3C(C4=C(C3=O)CCC=C4)=O)=C(C=C2)Cl)=O)C5=CC=CC(Cl)=C5)=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
[1]. Cody Aplin, et al. Defining the conformational states that enable transglutaminase 2 to promote cancer cell survival versus cell death. bioRxiv. 2024. [Content Brief]
[2]. Sabrina Schlienger, et al. ARF1 regulates adhesion of MDA-MB-231 invasive breast cancer cells through formation of focal adhesions. Cell Signal. 2015, 27, 3. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)