research use only
Cat.No.S8874
| Related Targets | EGFR VEGFR FGFR PDGFR c-Met Src MEK FLT3 HER2 c-Kit |
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| Other CSF-1R Inhibitors | Sotuletinib (BLZ945) Ki20227 Edicotinib(JNJ-40346527) Sulfatinib CSF1R-IN-1 Vimseltinib AZD7507 Chiauranib Adrixetinib TFA Pimicotinib |
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In vitro |
DMSO
: 79 mg/mL
(199.79 mM)
Water : Insoluble Ethanol : Insoluble The solubility data above are all experimental results (not literature values). |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.
Read more about PLX5622 working concentrations for cell culture treatment
PLX5622 is a potent inhibitor of CSF1R (< 10nM), CSF-1R (16 nM), c-kit (860 nM). PLX5622 exhibits the greatest inhibitory potency toward CSF1R (IC50 < 10nM).
| Information | PLX5622 is a potent, highly selective, and brain-penetrant CSF1R antagonist. It affects neuroinflammatory and microglial survival signaling by blocking CSF1R, effectively depleting microglia and suppressing neuroinflammation. |
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| Primary Applications and Mechanism of Action |
| Molecular Weight | 395.41 | Formula | C21H19F2N5O |
Storage (From the date of receipt) | 3 years -20°C powder |
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| CAS No. | 1303420-67-8 | -- | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC1=CC2=C(NC=C2CC3=C(N=C(C=C3)NCC4=C(N=CC(=C4)F)OC)F)N=C1 | ||
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