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CuATSP
🥰Excellent
Catalog No. T40791Cas No. 68341-12-8
Alias Cu-ATSP
CuATSP is a potent free radical trapping antioxidant (RTA) and ferroptosis inhibitor that reversibly adds a peroxyl radical to a bis (thiosemicarbazone) ligand to inhibit lipid peroxidation, showing therapeutic promise for diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson's disease.
CuATSP
🥰Excellent
Catalog No. T40791Alias Cu-ATSPCas No. 68341-12-8
CuATSP is a potent free radical trapping antioxidant (RTA) and ferroptosis inhibitor that reversibly adds a peroxyl radical to a bis (thiosemicarbazone) ligand to inhibit lipid peroxidation, showing therapeutic promise for diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson's disease.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $32 | In Stock | |
| 5 mg | $72 | In Stock | |
| 10 mg | $123 | In Stock | |
| 25 mg | $269 | In Stock | |
| 50 mg | $458 | In Stock | |
| 100 mg | $757 | In Stock | |
| 200 mg | $1,060 | In Stock |
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Product Introduction
Bioactivity
Chemical Properties
| Description | CuATSP is a potent free radical trapping antioxidant (RTA) and ferroptosis inhibitor that reversibly adds a peroxyl radical to a bis (thiosemicarbazone) ligand to inhibit lipid peroxidation, showing therapeutic promise for diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson's disease. |
| Alias | Cu-ATSP |
| Molecular Weight | 446.05 |
| Formula | C18H18CuN6S2 |
| Cas No. | 68341-12-8 |
| Smiles | [N-]1C(=[S][Cu+2]23[S]=C([N-][N]3=C(C(=[N]12)C)C)NC=4C=CC=CC4)NC=5C=CC=CC5 |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||
| Solubility Information | DMSO: 2 mg/mL (4.48 mM), Sonication and heating are recommended. | ||||||||||
Solution Preparation Table | |||||||||||
DMSO
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Sci Citations
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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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