中文名:PLX5622
英文名:PLX5622
英文别名:3-Pyridinemethanamine, 5-fluoro-N-[6-fluoro-5-[(5-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)methyl]-2-pyridinyl]-2-methoxy-
纯度:10mM in DMSO
货号:P409126
包装:1ml
Cas号:1303420-67-8
存储温度:-80℃储存
产品介绍:
Information
PLX5622 PLX5622 is a highly selective CSF-1R inhibitor (IC50 < 10 nmol/L), showing > 20-fold selectivity over KIT and FLT3.
In vitro
In vivo
In vivo PLX5622 demonstrates desirable PK properties in mice, rats, dogs, and monkeys, with a brain penetrance of ~20%. PLX5622 has low systemic clearance, moderate volume of distribution, and favorable oral bioavailability (F > 30%) in all four species. PLX5622 is a useful compound for investigating microglial dynamics. It allows for the sustained and specific elimination of microglia, preceding and during pathology development of Alzheimer’s disease (AD). Long-term PLX5622-mediated microglial depletion is highly robust, sustainable, and specific to the microglial compartment.
Cell Data
cell lines:Ba/F3 cells expressing JAK2V617F (Ba/F3-EpoR-V617F) and MPLW515L (Ba/F3-W515L) mutants.
Concentrations:
Incubation Time:
Powder Purity:≥98%
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关键字: 3-?Pyridinemethanamine, 5-?fluoro-?N-?[6-?fluoro-?5-?[(5-?methyl-?1H-?pyrrolo[2,?3-?b]?pyridin-?3-?yl)?methyl]?-?2-?pyridinyl]?-?2-?methoxy-
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