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(Rac)-AMXT-1501 4HCl is a polyamine transport inhibitor that inhibits polyamine transport and acts synergistically with cisplatin in HNSCC. (Rac)-AMXT-1501 4HCl has potential antimicrobial activity and inhibits neuroblastoma cell proliferation and pneumococcal pod biosynthesis by targeting ornithine decarboxylase and polyamine transport.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $183 | In Stock | In Stock | |
| 2 mg | $269 | In Stock | In Stock | |
| 5 mg | $456 | In Stock | In Stock | |
| 10 mg | $697 | In Stock | In Stock | |
| 25 mg | $1,530 | In Stock | In Stock | |
| 50 mg | $2,360 | - | In Stock |
| Description | (Rac)-AMXT-1501 4HCl is a polyamine transport inhibitor that inhibits polyamine transport and acts synergistically with cisplatin in HNSCC. (Rac)-AMXT-1501 4HCl has potential antimicrobial activity and inhibits neuroblastoma cell proliferation and pneumococcal pod biosynthesis by targeting ornithine decarboxylase and polyamine transport. |
| In vitro | In BE(2)-C, SMS-KCNR, and SH-SY5Y cells, AMXT-1501 tetrahydrochloride (0.39 µM, 1 µM, 3.1 µM, 10 µM, 31 µM, 50 µM; 48 hours) exhibited cytotoxicity against this panel of NB cell lines[2]. |
| In vivo | In C57BL/6 (WT) and experimental autoimmune encephalomyelitis (EAE) model-bearing ODC knockout strain (ODC cKO) mice, AMXT-1501 tetrahydrochloride (3 mg/kg; subcutaneous injection; once daily; 28 days) initially displayed a delayed disease onset but eventually proceeded with pathological development and reached the endpoint[3]. |
| Molecular Weight | 714.77 |
| Formula | C32H72Cl4N6O2 |
| Cas No. | 2771343-93-0 |
| Smiles | O=C(CCCCCCCCCCCCCCC)NCCCCC(C(NCCCNCCCCNCCCN)=O)N.Cl.Cl.Cl.Cl |
| Relative Density. | no data available |
| Storage | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: 72.5 mg/mL (101.43 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
H2O
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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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