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UAMC00039 dihydrochloride

🥰Excellent
Catalog No. T4467Cas No. 697797-51-6
Alias UAMC 00039 dihydrochloride

UAMC00039 dihydrochloride is a potent, reversible, and competitive inhibitor of dipeptidyl peptidase II, with an IC50 of 0.48 nM.

UAMC00039 dihydrochloride

UAMC00039 dihydrochloride

🥰Excellent
Purity: 99.56%
Catalog No. T4467Alias UAMC 00039 dihydrochlorideCas No. 697797-51-6
UAMC00039 dihydrochloride is a potent, reversible, and competitive inhibitor of dipeptidyl peptidase II, with an IC50 of 0.48 nM.
Pack SizePriceAvailabilityQuantity
1 mg$37In Stock
5 mg$101In Stock
10 mg$163In Stock
25 mg$328In Stock
50 mg$496In Stock
100 mg$693In Stock
1 mL x 10 mM (in DMSO)$85In Stock
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Purity:99.56%
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Product Introduction

Bioactivity
Description
UAMC00039 dihydrochloride is a potent, reversible, and competitive inhibitor of dipeptidyl peptidase II, with an IC50 of 0.48 nM.
Targets&IC50
DPP2:0.48 nM.
Kinase Assay
Stability of UAMC00039 in RPMI medium or assay buffer (50 mM cacodylate buffer pH5.5) is monitored at 37 °C. The inhibitors' capacity (IC50) to inhibit DPPII is measured at different time points (up to 48 h). U937 cells are incubated with various concentrations of UAMC00039 for 15 min at 37 °C in RPMI. Cells are then ished with PBS, lysed and assayed for DPPII activity. Concentration–response and time–response curves are generated from incubations of PBMC with UAMC00039 (0.01 nM–1 μM) in RPMI at 37 °C for 1, 5, 15, 30 and 60 min. Ished cells are lysed overnight at 4 °C using 100 mM HEPES buffer pH 7.4, 10 mM EDTA, 70 μg/mL aprotinin and 1% octylglucoside.
Animal Research
Rat: UAMC00039 is administered orally at 2 mg/kg (~5 μMol/kg in a vehicle of 2% tween 80, 10 mL/kg) on a blind basis in all in vivo assays. For each assay, a reference compound and vehicle control is analyzed concurrently. For the in vivo studies 3 to 5 animals per condition are tested.
AliasUAMC 00039 dihydrochloride
Chemical Properties
Molecular Weight382.76
FormulaC16H26Cl3N3O
Cas No.697797-51-6
SmilesCl.Cl.N[C@@H](CCNCc1ccc(Cl)cc1)C(=O)N1CCCCC1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 55 mg/mL (143.69 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6126 mL13.0630 mL26.1260 mL130.6302 mL
5 mM0.5225 mL2.6126 mL5.2252 mL26.1260 mL
10 mM0.2613 mL1.3063 mL2.6126 mL13.0630 mL
20 mM0.1306 mL0.6532 mL1.3063 mL6.5315 mL
50 mM0.0523 mL0.2613 mL0.5225 mL2.6126 mL
100 mM0.0261 mL0.1306 mL0.2613 mL1.3063 mL

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In Vivo Formulation Calculator (Clear solution)

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.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
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Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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