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DDO-2728

(Synonyms: DDO2728, DDO 2728) Copy Product Info
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Synonyms: DDO2728, DDO 2728

Catalog No. T205009 Copy Product Info
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DDO-2728 is a selective pyrazolo[1,5-a]pyrimidine-based ALKBH5 inhibitor with an IC50 of 2.97 μM. It increases the levels of N6-methyladenosine (m6A) modifications in acute myeloid leukemia (AML) cells and exhibits antiproliferative activity in these cells. DDO-2728 also demonstrates anti-tumor efficacy in the MV4-11 xenograft model.
DDO-2728
Cas No. 3029515-97-4
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
DDO-2728 is a selective pyrazolo[1,5-a]pyrimidine-based ALKBH5 inhibitor with an IC50 of 2.97 μM. It increases the levels of N6-methyladenosine (m6A) modifications in acute myeloid leukemia (AML) cells and exhibits antiproliferative activity in these cells. DDO-2728 also demonstrates anti-tumor efficacy in the MV4-11 xenograft model.
Targets & IC50
HUVEC:165.1 μM, HEK293 cells:97.4 μM, MOLM-13 cells:0.45 μM, MV4-11 cells:1.2 μM
In vitro
DDO-2728 (0–40 μM, 48 h) increased m6A methylation levels in MOLM-13, HEK293, and MV4-11 cells across a concentration gradient [1].
DDO-2728 (0.01–100 μM, 72 h) inhibits the proliferation of MOLM-13 and MV4-11 cells, with IC₅₀ values of 0.45 and 1.2 μM, respectively, and exhibits relatively low toxicity toward HEK293 and HUVEC cells [1].
DDO-2728 (20 μM, 48 h) significantly arrested the cell cycle of MOLM-13 and MV4-11 cells at the G1/M phase [1].
DDO-2728 (5, 10 μM, 48 h) induced apoptosis in MV4-11 and MOLM-13 cells in a concentration-dependent manner [1].
DDO-2728 (20 μM, 24 h) reduced the half-life of TACC3 mRNA in MOLM-13 and MV4-11 cells [1].
DDO-2728 (0–10 μM, 48 h) significantly reduced the abundance of TACC3 and c-Myc in MOLM-13 and MV4-11 cells at both the mRNA and protein levels [1].
In vivo
DDO-2728 (10–40 mg/kg, intraperitoneal injection, once daily, for 14 days) effectively inhibited tumor growth in nude mice with MV4-11 xenografts [1].
SynonymsDDO2728, DDO 2728
Chemical Properties
Molecular Weight578.45
FormulaC28H17F3N4O7
Cas No.3029515-97-4
SmilesO=C(C1=CC=C(C2=NN3C=C(C(C4=C(O)C([N+]([O-])=O)=CC=C4O)=O)C=NC3=C2)C=C1)OCC5=CC=C(C(F)(F)F)C=C5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 100.00 mg/mL (172.88 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.7288 mL8.6438 mL17.2876 mL86.4379 mL
5 mM0.3458 mL1.7288 mL3.4575 mL17.2876 mL
10 mM0.1729 mL0.8644 mL1.7288 mL8.6438 mL
20 mM0.0864 mL0.4322 mL0.8644 mL4.3219 mL
50 mM0.0346 mL0.1729 mL0.3458 mL1.7288 mL
100 mM0.0173 mL0.0864 mL0.1729 mL0.8644 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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 stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Related Tags: DDO-2728 chemical structure | DDO-2728 in vivo | DDO-2728 in vitro | DDO-2728 formula | DDO-2728 molecular weight