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PLX5622
Catalog No. T7100Cas No. 1303420-67-8
Alias PLX-5622
PLX5622 is a highly selective, brain-penetrant, and orally active CSF1R inhibitor.
PLX5622
Catalog No. T7100Alias PLX-5622Cas No. 1303420-67-8
PLX5622 is a highly selective, brain-penetrant, and orally active CSF1R inhibitor.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $97 | In Stock | |
| 10 mg | $161 | In Stock | |
| 25 mg | $324 | In Stock | |
| 50 mg | $537 | In Stock | |
| 100 mg | $649 | In Stock | |
| 500 mg | $1,380 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $86 | In Stock |
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Purity:99.89%
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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 | PLX5622 is a highly selective, brain-penetrant, and orally active CSF1R inhibitor. |
| Targets&IC50 | CSF1R:Ki: 5.9 nM, CSF1R:0.016 µM (IC50) |
| In vitro | METHODS: CX CR1+/GFP mouse-derived mixed glial cell cultures were treated with PLX5622 (0.1-10 µM) for 7 days and cell counts were assayed by Flow cytometry. RESULTS: Although there was a dose-dependent decrease in microglia numbers under PLX5622, no decrease in GFAP+ astrocytes was seen, but rather a gradual increase, along with a decrease in PDGFR-a OPC. [1] METHODS: Cerebellar sections prepared from PLP-eGFP mouse pups were treated with PLX5622 (1-20 µM) for 3 days followed by Immunostaining. RESULTS: After three days of treatment, PLX5622 at concentrations greater than 2 µM eliminated more than 95% of microglia. [2] |
| In vivo | METHODS: To study in vivo activity, PLX5622 (1200 mg/kg) was administered to PLP eGFP mice by feed for 7-21 days. RESULTS: PLX5622 was effective in depleting microglia in the central nervous system of adult mice. treatment with PLX5622 for 7 days had no effect on oligodendrocyte progenitor cell populations; however, a mild reduction was observed after 21 days in some central nervous system regions. [2] |
| Alias | PLX-5622 |
| Molecular Weight | 395.41 |
| Formula | C21H19F2N5O |
| Cas No. | 1303420-67-8 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 16.67 mg/mL (42.15 mM), Sonication is recommended.  10% DMSO+40% PEG300+5% Tween 80+45% Saline: 7.9 mg/mL (19.98 mM), Suspension. Please add co-solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
10% DMSO+40% PEG300+5% Tween 80+45% Saline/DMSO
DMSO
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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% 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.
Dose Conversion
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