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Synonyms: DDO2728, DDO 2728

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| 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]. |
| Synonyms | DDO2728, DDO 2728 |
| Molecular Weight | 578.45 |
| Formula | C28H17F3N4O7 |
| Cas No. | 3029515-97-4 |
| Smiles | O=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 | Powder: -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
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. | ||||||||||||||||||||||||||||||||||||
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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