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(-)-Agelastatin A is a member of the pyrrole-aminoimidazole marine alkaloid (PAI) family, capable of inhibiting β-catenin, GSK-3β, and osteopontin (OPN), exhibiting antiproliferative activity against various cancers such as leukaemia and breast cancer, and possessing a certain ability to penetrate the central nervous system (CNS).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $490 | - | In Stock | |
| 5 mg | $1,090 | - | In Stock | |
| 10 mg | $1,480 | - | In Stock | |
| 25 mg | $2,230 | - | In Stock | |
| 50 mg | $2,950 | - | In Stock |
| Description | (-)-Agelastatin A is a member of the pyrrole-aminoimidazole marine alkaloid (PAI) family, capable of inhibiting β-catenin, GSK-3β, and osteopontin (OPN), exhibiting antiproliferative activity against various cancers such as leukaemia and breast cancer, and possessing a certain ability to penetrate the central nervous system (CNS). |
| Targets&IC50 | Jurkat cells:74 nM, U-937 cells:67 nM, BT-549 cells:278 nM, IMR90 cells:1.11 μM, HL-60 cells:138 nM, CEM cells:20 nM, CA46 cells:187 nM, HeLa cells:708 nM, Daudi cells:20 nM, A549 cells:1.05 μM |
| In vitro | Methods: Agelastatin A (0-2 μM, 48 h) was used to treat U-937, HeLa, A549, BT549 and IMR90 cells, and the IC50 values at 48 hours were determined by MTS. Results: The IC50 values of U-937, HeLa, A549, BT549 and IMR90 cells were 67 nM, 708 nM, 1.05 μM, 278 nM and 1.11 μM, respectively. Methods: CEM, Jurkat, Daudi, HL-60 and CA46 cells were treated with Agelastatin A (0-1 μM, 48 h). The IC50 values at 48 h were determined by MTS assay. Results: The IC50 values of CEM, Jurkat, Daudi, HL-60 and CA46 cells were 20, 74, 20, 138 and 187 nM, respectively. [1] |
| Synonyms | AglA, Agelastatin A |
| Molecular Weight | 341.16 |
| Formula | C12H13BrN4O3 |
| Cas No. | 152406-28-5 |
| Smiles | BrC=1N2[C@]3([C@]([C@]4([C@@](O)(C3)N(C)C(=O)N4)[H])(NC(=O)C2=CC1)[H])[H] |
| Relative Density. | 2.24 g/cm3 (Predicted) |
| Storage | store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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