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Z-MAL is an efficient, broad-spectrum substrate for HDAC. It exhibits potent conversion activity for both Class I and II histone deacetylases as well as Class III SIRT1. Z-MAL is utilized in research focused on the structure-activity relationship, subtype selectivity, and inhibitor screening of HDAC.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Z-MAL is an efficient, broad-spectrum substrate for HDAC. It exhibits potent conversion activity for both Class I and II histone deacetylases as well as Class III SIRT1. Z-MAL is utilized in research focused on the structure-activity relationship, subtype selectivity, and inhibitor screening of HDAC. |
| Molecular Weight | 479.53 |
| Formula | C26H29N3O6 |
| Cas No. | 642463-22-7 |
| Smiles | CC=1C=2C(=CC(NC([C@@H](NC(OCC3=CC=CC=C3)=O)CCCCNC(C)=O)=O)=CC2)OC(=O)C1 |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
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