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D-Cl-amidine hydrochloride, a potent and highly selective inhibitor of PAD1, exhibits excellent tolerance and does not induce significant toxicity [1].
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 100 mg | $1,490 | 10-14 weeks | 10-14 weeks |
| Description | D-Cl-amidine hydrochloride, a potent and highly selective inhibitor of PAD1, exhibits excellent tolerance and does not induce significant toxicity [1]. |
| In vitro | D-Cl-amidine (200-400 μM) effectively reduces cell viability and increases caspase 3 activity in MDA-MB-231 cells, suggesting that inhibition of PAD1 enhances apoptosis [1]. |
| In vivo | Administered intravenously (iv) at a dose of 2.5 mg/kg, D-Cl-amidine remains detectable in serum, exhibiting concentrations of approximately 21 nM after 2 hours and around 10 nM at 4 hours. Similarly, when administered intraperitoneally (ip) at a 10 mg/kg dosage, D-Cl-amidine's presence in blood serum is sustained, with concentrations approximately 10 nM at the 4-hour mark [1]. |
| Molecular Weight | 347.24 |
| Formula | C14H20Cl2N4O2 |
| Smiles | #N/A |
| 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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