CDK2-IN-59
CDK2-IN-59 is a CDK2 inhibitor with a IC50 of 66.33 μM. CDK2-IN-59 stably interacts within the CDK2 active site and induces apoptosis in breast cancer cells. CDK2-IN-59 can be used for the research of breast cancer.
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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: C24H18ClN5O4
- 分子量:475.88
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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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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CDK2/CycA2 66.33 μM (IC50) |
CDK2-IN-59 (Compound 7d) (up to 500 μM) potently inhibits the proliferation of MDA-MB-231 breast cancer cells with an IC50 of 5.16 μM[1].
CDK2-IN-59 exhibits reduced cytotoxicity toward L929 murine fibroblast normal cells with an IC50 of 59.10 μM and a selectivity index of 11.45 compared to MDA-MB-231 breast cancer cells[1].
CDK2-IN-59 induces apoptosis in MDA-MB-231 breast cancer cells, driving 14.1% of cells into early apoptosis and 52.7% into late apoptosis[1].
CDK2-IN-59 significantly inhibits CDK2/CyclinA2 enzymatic activity with an IC50 of 66.33 μM[1].
CDK2-IN-59 exhibits strong binding affinity for CDK2 (PDB ID: 4BCQ) with an MM/GBSA binding free energy of -53.28 kcal/mol[1].
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 475.88
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分子式 C24H18ClN5O4
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SMILES
COC1=CC=C(C2=CC(C3=CC=C(OC4=NC(N)=NC(Cl)=C4)C=C3)=C(C#N)C(N2)=O)C=C1OC
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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)
CDK2-IN-59 関連分類
HY-183789 関連分類
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