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HDAC-IN-93 is an HDAC inhibitor that demonstrates strong, broad-spectrum inhibitory activity against HDACs. It exhibits significant antiproliferative effects on various cancer cell lines and can induce apoptosis (apoptosis) and necrosis. HDAC-IN-93 is applicable for research in prostate and breast cancer.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | HDAC-IN-93 is an HDAC inhibitor that demonstrates strong, broad-spectrum inhibitory activity against HDACs. It exhibits significant antiproliferative effects on various cancer cell lines and can induce apoptosis (apoptosis) and necrosis. HDAC-IN-93 is applicable for research in prostate and breast cancer. |
| In vitro | HDAC-IN-93 (Compound 17) exhibits sensitivity towards a variety of cancer cell lines, showing particular efficacy in prostate cancer PC-3 cells and breast cancer MCF-7 cells, with IC50 values of 4.1 μM and 20.8 μM, respectively. At a concentration of 4.1 μM for 24 hours, HDAC-IN-93 markedly increases the number of SubG0-G1 phase cells and induces early apoptosis in MCF-7 cells. This compound also upregulates pro-apoptotic genes (Bax, Cyt-C, Caspase-3) and downregulates the anti-apoptotic gene (Bcl-2) in MCF-7 cells. HDAC-IN-93 demonstrates a total HDAC inhibitory activity of 66.1% in MCF-7 cells, although it exhibits weaker direct inhibition on specific HDAC subtypes (6, 7, 8). |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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