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(Rac)-AMXT-1501 4HCl
🥰Excellent
Catalog No. T10313Cas No. 2771343-93-0
(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.
(Rac)-AMXT-1501 4HCl
🥰Excellent
Purity: 98.31%
Catalog No. T10313Cas No. 2771343-93-0
(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 | Availability | Quantity |
|---|---|---|---|
| 1 mg | $183 | In Stock | |
| 2 mg | $269 | In Stock | |
| 5 mg | $456 | In Stock | |
| 10 mg | $697 | In Stock | |
| 25 mg | $1,530 | In Stock | |
| 50 mg | $2,360 | In Stock |
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CitedSelect Batch
Purity:98.31%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| 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 & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
| Solubility Information | H2O: 60 mg/mL (83.94 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
H2O
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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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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