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NVP-DPP728 dihydrochloride

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Catalog No. T39481Cas No. 207556-62-5
Alias NVP-DPP728 dihydrochloride

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.

NVP-DPP728 dihydrochloride

NVP-DPP728 dihydrochloride

😃Good
Catalog No. T39481Alias NVP-DPP728 dihydrochlorideCas No. 207556-62-5
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.
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Product Introduction

Bioactivity
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.
AliasNVP-DPP728 dihydrochloride
Chemical Properties
Molecular Weight371.27
FormulaC15H20Cl2N6O
Cas No.207556-62-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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2 Enter the in vivo formulation:
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