Antitumor agent-223
Antitumor agent-223 is an anticancer agent and TRK inhibitor. Antitumor agent-223 exerts potent antitumor activity against liver cancer and breast cancer. Antitumor agent-223 can be used for the research of hepatocellular carcinoma and breast cancer.
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- CAS No.: 3124621-78-6
- Formule: C24H22F4N4O
- Masse moléculaire:458.45
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
In Vitro
Antitumor agent-223 (Compound IIIc) potently inhibits the proliferation of HepG2 hepatocellular carcinoma cells (IC50 = 2.06 μM) and MCF-7 breast cancer cells (IC50 = 3.15 μM)[1].
Antitumor agent-223 (1-7 μM; 48-96 h) effectively inhibits the migration of HepG2 hepatocellular carcinoma cells in a concentration- and time-dependent manner, with a migration rate of 16.70% after treatment at 7 μM for 96 h[1].
Antitumor agent-223 (1-5 μM) potently reduces the colony-forming ability of HepG2 hepatocellular carcinoma cells, with a colony formation rate of 12.50% at 5 μM and 38.20% at 3 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:HepG2 hepatocellular carcinoma cells
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Concentration:1-5 μM (48 h, 96 h); 7 μM (96 h)
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Incubation Time:48 h, 96 h
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Result:Inhibits HepG2 cell migration in a concentration- and time-dependent manner.
Reduces the cell migration rate to 16.70% at 7 μM for 96 h (compared to the control group's 70.08%, P < 0.01).
Reduces migration rates relative to controls at 1 μM, 3 μM, and 5 μM at both 48 h and 96 h.
Chemical Information
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CAS No. 3124621-78-6
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Masse moléculaire 458.45
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Formule C24H22F4N4O
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SMILES
O=C(N1)/C(C2=C1C=CC(NCC3=C(F)C=CC(C(F)(F)F)=C3)=C2)=C\C4=CN=C(CCCC)N4
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocole
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Liver Cancer Modeling
Liver cancer can be classified into primary liver cancer and secondary liver cancer. Secondary liver cancer is the metastatic liver cancer. Primary liver cancer includes hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC) and fibrolamellar HCC, of which HCC is the most common form, accounting for approximately 90% of primary liver cancers[1]. HCC mouse models include chemical agent-induced models, transplanted tumor models, and genetic engineered models.
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Subcutaneous Cell-Line-Derived Xenograft
Subcutaneous cell-line-derived xenograft (CDX) models are established by implanting cultured human cancer cell lines into immunodeficient mice, where the injected cells form localized tumors that can be monitored in vivo as a measure of tumorigenic potential, growth kinetics, and treatment response. These models are widely used in oncology research because they allow reproducible tumor formation and enable comparative assessment of tumor growth between different cell lines or genetic manipulations in a controlled in vivo microenvironment. Subcutaneous implantation of cancer cells in immunodeficient mice is a standard approach for evaluating tumor growth behavior and therapeutic response across multiple cancer types, including prostate, esophageal, pancreatic, and colon cancer models.
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Breast Cancer Modeling
Breast cancer is a heterogeneous cancer, and it has been distinguished into four subtypes: luminal A, luminal B, HER2-positive and basal-like. Molecular mutations, epigenetic alterations, hormone exposure and immune microenvironment are related to the progression of breast cancer.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)