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NVP-DPP728 dihydrochloride is a highly potent, selective, and orally active inhibitor of dipeptidyl peptidase IV (DPP-IV), with a binding affinity (K i ) of 11 nM. This compound proves useful for investigating diabetes mellitus in research studies.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | Inquiry | Inquiry |
| Description | NVP-DPP728 dihydrochloride is a highly potent, selective, and orally active inhibitor of dipeptidyl peptidase IV (DPP-IV), with a binding affinity (K i ) of 11 nM. This compound proves useful for investigating diabetes mellitus in research studies. |
| Targets&IC50 | DPP4:11 nM (Ki) |
| In vitro | NVPDPP728 selectively inhibits DPP-IV in both human and rat plasma, exhibiting high potency with IC50 values between 5-10 nM. Its selectivity exceeds 15,000-fold compared to DPP-II and various proline-cleaving proteases[1]. |
| In vivo | NVP-DPP728 (3.72 mg/kg; p.o.) suppresses DPP-IV, likely amplify ng endogenous GLP-1 effects to enhance insulin secretion and glucose tolerance in obese (fa/fa) and lean (FA/?) Zucker rats, as evidenced by inhibited plasma DPP-IV activity. |
| Synonyms | NVP-DPP728 dihydrochloride |
| Molecular Weight | 371.27 |
| Formula | C15H20Cl2N6O |
| Cas No. | 207556-62-5 |
| Smiles | Cl.Cl.O=C(CNCCNc1ccc(cn1)C#N)N1CCC[C@H]1C#N |
| 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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