PLX5622 NEW
| Price | $97 | $161 | $324 |
| Package | 5mg | 10mg | 25mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2025-06-16 |
Product Details
| Product Name: PLX5622 | CAS No.: 1303420-67-8 |
| Purity: 99.32% | Supply Ability: 10g |
| Release date: 2025/06/16 |
Product Introduction
Bioactivity
| Name | PLX5622 |
| Description | PLX5622 is a highly selective, brain-penetrant, and orally active CSF1R inhibitor. |
| 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] |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice./Shipping at ambient temperature. |
| 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. |
| Keywords | preceding | PLX5622 | PLX 5622 | penetrant | pathology | orally | microglial | Inhibitor | inhibit | elimination | CSF-1R | CSF1R | CSF-1 receptor | colony stimulating factor 1 receptor | c-Fms | cFms | brain |
| Inhibitors Related | c-Fms-IN-3 | PLX647 | Sotuletinib | Tandutinib | AZD7507 | GW2580 | Pexidartinib | c-Fms-IN-13 | GW786034B | Linifanib | Masitinib | Cerdulatinib hydrochloride |
| Related Compound Libraries | Highly Selective Inhibitor Library | Bioactive Compound Library | Cytokine Inhibitor Library | Membrane Protein-targeted Compound Library | Kinase Inhibitor Library | Tyrosine Kinase Inhibitor Library | Drug Repurposing Compound Library | CNS-Penetrant Compound Library | Inhibitor Library | Bioactive Compounds Library Max | Fluorochemical Library | Anti-COVID-19 Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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United States- Since: 2011-01-07
- Address: 36 Washington Street, Wellesley Hill, MA
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