ChemicalBook--->CAS DataBase List--->2040295-03-0

2040295-03-0

2040295-03-0 Structure

2040295-03-0 Structure
IdentificationBack Directory
[Name]

PLX3397 HCl
[CAS]

2040295-03-0
[Synonyms]

PLX3397 HCl
Pexidartinib hcl
Pexidartinib Hydrochloride Salt
Pexidartinib hydrochloride (PLX-3397)
[Molecular Formula]

C20H16Cl2F3N5
[MDL Number]

MFCD30738678
[MOL File]

2040295-03-0.mol
[Molecular Weight]

454.28
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:60.0(Max Conc. mg/mL);132.1(Max Conc. mM)
[form ]

Solid
[color ]

White to off-white
[InChIKey]

CJLUYLRKLUYCEK-UHFFFAOYSA-N
[SMILES]

C(C1=CN=C(NCC2=CN=C(C(F)(F)F)C=C2)C=C1)C1=CNC2=NC=C(Cl)C=C12.Cl
Hazard InformationBack Directory
[Uses]

Pexidartinib Hydrochloride is RTK inhibitor. It can be used in pharmacological activity, therapeutic use, and biological study of inhibition of colony stimulating factor-1 receptor improves antitumor efficacy of BRAF inhibition.
[in vivo]

Pexidartinib can be used to deplete the microglia cells in mice.
Pexidartinib (290 ppm in AIN-76A standard chow, 21 days) depletes the microglia cells in brain by 70% in adult male C57BL/6?J mice (20–25?g)[5].
Pexidartinib (600 ppm in chow, 10 days and 30 days ) depletes the microglia cells more than 90% in brain of C57BL/6J mice[6].
Pexidartinib hydrochloride (0.25, 1 mg/kg, i.p., twice daily for 8 days) inhibits the proliferation of microglia and BrdU-positive cells in neonatal mice[2].
Pexidartinib hydrochloride (1 mg/kg, twice daily for 8 day) shows no obvious effect on the cleaved caspase-3-positive cells in mice[2].
Pexidartinib hydrochloride (50 mg/kg; p.o.; every second day for 3 weeks) reduces tissue macrophage levels without affecting glucose homeostasis in mice[4].

Animal Model:Neonatal mice[2]
Dosage:0.25, 1 mg/kg
Administration:I.P. twice daily for 8 days
Result:Decreased the number of microglia and BrdU-positive proliferative cells, but did not change the cleaved caspase-3-positive cells.
Animal Model:10-week old litter mate C57BL/6 mice (chow and high-fat diet fed mice)[4]
Dosage:50?mg/kg
Administration:P.o.; every second day for 3 weeks
Result:Substantially reduced macrophage numbers in adipose tissue of both chow and high-fat diet fed mice without affecting total myeloid cell levels.
[storage]

Store at -20°C
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