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1G244

Catalog No. T14005Cas No. 847928-32-9

1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties. 1G244 had the IC50 values of 14 and 53 nM against DPP8 and DPP9, and The Ki values for 1G244 were 0.9 and 4.2 nM for DPP8 and DPP9

1G244

1G244

Purity: 98.23%
Catalog No. T14005Cas No. 847928-32-9
1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties. 1G244 had the IC50 values of 14 and 53 nM against DPP8 and DPP9, and The Ki values for 1G244 were 0.9 and 4.2 nM for DPP8 and DPP9
Pack SizePriceAvailabilityQuantity
5 mg$33In Stock
10 mg$53In Stock
25 mg$106In Stock
50 mg$173In Stock
100 mg$283In Stock
500 mgInquiryIn Stock
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Purity:98.23%
ee:98.76%
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Product Introduction

Bioactivity
Description
1G244 is an inhibitor of DPP8/9 with antiatherosclerotic and antimyeloma properties. 1G244 had the IC50 values of 14 and 53 nM against DPP8 and DPP9, and The Ki values for 1G244 were 0.9 and 4.2 nM for DPP8 and DPP9
Targets&IC50
DPP8:0.9 nM(ki), DPP9:53 nM, DPP8:14 nM, DPP9:4.2 nM(ki)
In vitro
1G244 (0-100 μM) dose-dependently decreased viable cell number of five multiple myeloma cell lines as well as three T-cell lymphoma cell lines[2].
In vivo
The apoE−/− mice treated with 1G244 (1G244 dissolved in 75% PEG 300, 2 mg/kg) showed that 1G244 reduced the area of advanced atherosclerotic lesions by about 14%[1]. 1G244 was administered subcutaneously into mice at 30 mg/kg once a week, administration of 1G244 apparently suppressed the subcutaneous growth of MM.1 S cells[2].
Chemical Properties
Molecular Weight504.57
FormulaC29H30F2N4O2
Cas No.847928-32-9
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 225.0 mg/mL (445.9 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9819 mL9.9094 mL19.8189 mL99.0943 mL
5 mM0.3964 mL1.9819 mL3.9638 mL19.8189 mL
10 mM0.1982 mL0.9909 mL1.9819 mL9.9094 mL
20 mM0.0991 mL0.4955 mL0.9909 mL4.9547 mL
50 mM0.0396 mL0.1982 mL0.3964 mL1.9819 mL
100 mM0.0198 mL0.0991 mL0.1982 mL0.9909 mL

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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
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