1. PI3K/Akt/mTOR Cell Cycle/DNA Damage MAPK/ERK Pathway Stem Cell/Wnt Apoptosis
  2. Akt PI3K PERK p38 MAPK ERK Apoptosis
  3. Anticancer agent 319

Anticancer agent 319 is an anticancer agent. Anticancer agent 319 inhibits the proliferation of liver cancer cells. Anticancer agent 319 inhibits AKT phosphorylation and blocks the PI3K/AKT signaling axis; meanwhile, it inhibits ERK1/2 phosphorylation and blocks the MAPK/ERK signaling axis. Anticancer agent 319 induces G2/M phase cell cycle arrest, triggers apoptosis, and reduces mitochondrial membrane potential in liver cancer cells. Anticancer agent 319 can be used for the research of hepatocellular carcinoma.

For research use only. We do not sell to patients.

Anticancer agent 319

Anticancer agent 319 Chemical Structure

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Description

Anticancer agent 319 is an anticancer agent. Anticancer agent 319 inhibits the proliferation of liver cancer cells. Anticancer agent 319 inhibits AKT phosphorylation and blocks the PI3K/AKT signaling axis; meanwhile, it inhibits ERK1/2 phosphorylation and blocks the MAPK/ERK signaling axis. Anticancer agent 319 induces G2/M phase cell cycle arrest, triggers apoptosis, and reduces mitochondrial membrane potential in liver cancer cells. Anticancer agent 319 can be used for the research of hepatocellular carcinoma[1].

In Vitro

Anticancer agent 319 (Compound 11e) (48-72 h) potently inhibits the proliferation of human hepatocellular carcinoma cells HepG2 and Hep3B, with IC50 values of 2.22 μM (72 h, HepG2), 4.55 μM (48 h, HepG2) and 4.95 μM (48 h, Hep3B), respectively, but exerts no inhibitory effect on the proliferation of Huh-7 cells[1].
Anticancer agent 319 (2.5-10 μM; 24-48 h) inhibits the migration of human hepatocellular carcinoma cell line HepG2 in a dose-dependent manner[1].
Anticancer agent 319 (2.5-10 μM; 36-48 h) induces G2/M cell cycle arrest, triggers concentration-dependent apoptosis, and reduces mitochondrial membrane potential in human hepatocellular carcinoma HepG2 cells[1].
Anticancer agent 319 (2.5-10 μM; 36 h) dose-dependently inhibits the phosphorylation of AKT (Ser473) and ERK1/2 (Thr202/Tyr204), and blocks the PI3K/AKT and MAPK/ERK signaling axes in human hepatocellular carcinoma HepG2 cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Migration Assay [1]

Cell Line: human hepatocellular carcinoma HepG2 cells
Concentration: 2.5, 5 and 10 μM
Incubation Time: 24 h; 48 h
Result: Inhibited HepG2 cell migration in a dose-dependent manner.
Reduced the wound closure rate to 52.96% (2.5 μM), 27.41% (5 μM), and 13.45% (10 μM) after 48 h, compared to 59.11% in the control group.

Cell Cycle Analysis[1]

Cell Line: human hepatocellular carcinoma HepG2 cells
Concentration: 2.5, 5 and 10 μM
Incubation Time: 36 h
Result: Induced G2/M phase arrest at all concentrations.
Increased the SubG1 (apoptotic) population to approximately 22.33% at 5 μM and 10 μM, indicating DNA fragmentation and apoptosis.

Apoptosis Analysis[1]

Cell Line: human hepatocellular carcinoma HepG2 cells
Concentration: 2.5, 5 and 10 μM
Incubation Time: 48 h
Result: Induced characteristic apoptotic nuclear changes, including condensation and fragmentation, in a dose-dependent manner.
Control cells showed uniform, pale blue nuclear staining.\nIncreased the proportion of both early and late apoptotic cells in a concentration-dependent manner.
Caused significant reductions in viable cells compared to the control.

Western Blot Analysis[1]

Cell Line: human hepatocellular carcinoma HepG2 cells
Concentration: 2.5, 5 and 10 μM
Incubation Time: 36 h
Result: Dose-dependently inhibited the phosphorylation of AKT (Ser473) and ERK1/2 (Thr202/Tyr204).
Nearly completely suppressed phosphorylation at the highest concentration.
Molecular Weight

657.54

Formula

C33H34Cl2N2O8

SMILES

COC([C@@H](NC(CCC(OCCOC1=CC2=C(C3=CC=CC=C3C(O2)=O)C=C1)=O)=O)CC4=CC=C(C=C4)N(CCCl)CCCl)=O

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

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Product Name:
Anticancer agent 319
Cat. No.:
HY-183316
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