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Fodipir
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Catalog No. T19327Cas No. 118248-91-2
Alias DPDP
Fodipir, the active metabolite of mangafodipir, plays a crucial role in the mechanism of mangafodipir-mediated cytoprotection, specifically mitigating cell death induced by 7β-hydroxycholesterol.
Fodipir
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Catalog No. T19327Alias DPDPCas No. 118248-91-2
Fodipir, the active metabolite of mangafodipir, plays a crucial role in the mechanism of mangafodipir-mediated cytoprotection, specifically mitigating cell death induced by 7β-hydroxycholesterol.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $30 | 5 days | 5 days |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
| Description | Fodipir, the active metabolite of mangafodipir, plays a crucial role in the mechanism of mangafodipir-mediated cytoprotection, specifically mitigating cell death induced by 7β-hydroxycholesterol. |
| In vitro | Fodipir (Dp-dp; Dipyridoxyl diphosphate; 100 μM) demonstrates significant cytoprotective effects, effectively mitigating 7β-hydroxycholesterol (7β-OH)-induced cell death after 8 hours of treatment. It not only reduces cellular reactive oxygen species (ROS) production triggered by 7β-OH but also inhibits lysosomal membrane permeabilization (LMP), enhancing cell survival. Fodipir, as a principal metabolite of mangafodipir, plays a crucial role in the cytoprotection conferred by mangafodipir against 7β-OH-induced cytotoxicity. |
| Synonyms | DPDP |
| Molecular Weight | 638.46 |
| Formula | C22H32N4O14P2 |
| Cas No. | 118248-91-2 |
| Relative Density. | 1.657 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
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% Saline/PBS/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 μLSaline/PBS/ddH2O 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 μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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