Powder: -20°C for 3 years | In solvent: -80°C for 1 year
HDAC-IN-42 (compound 14f) is a highly potent and selective inhibitor of histone deacetylase (HDAC) enzymes, with IC50 values of 0.19 μM for HDAC1 and 4.98 μM for HDAC6. It exhibits remarkable anticancer properties and inhibits cell proliferation. Additionally, HDAC-IN-42 induces apoptosis and causes cell cycle arrest specifically at the G2/M phase [1].
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 6-8 weeks | $ 2,140.00 | |
50 mg | 6-8 weeks | $ 2,785.00 | |
100 mg | 6-8 weeks | $ 3,520.00 |
Description | HDAC-IN-42 (compound 14f) is a highly potent and selective inhibitor of histone deacetylase (HDAC) enzymes, with IC50 values of 0.19 μM for HDAC1 and 4.98 μM for HDAC6. It exhibits remarkable anticancer properties and inhibits cell proliferation. Additionally, HDAC-IN-42 induces apoptosis and causes cell cycle arrest specifically at the G2/M phase [1]. |
In vitro | HDAC-IN-42 (compound 14f) exhibits anti-proliferative effects on various cancer cell lines, achieving half-maximal inhibitory concentrations (C50s) of 9.56 μM for MCF-7, 13.32 μM for HCT-116, 10.46 μM for HepG2, and 6.91 μM for HeLa cells. At concentrations of 1, 5, and 10 μM over 24 hours, it diminishes colony formation in HeLa cells and enhances the expression levels of histone H3 and α-tubulin, indicating an impact on cell structure and genetic material packaging. Furthermore, when applied for 48 hours, HDAC-IN-42 prompts apoptosis and halts the cell cycle at the G2/M phase, demonstrating its potential as a targeted therapeutic agent [1]. |
Molecular Weight | 381.34 |
Formula | C20H15NO7 |
CAS No. | 2454024-18-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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HDAC-IN-42 2454024-18-9 inhibitor inhibit