ChemicalBook--->CAS DataBase List--->1700663-41-7

1700663-41-7

1700663-41-7 Structure

1700663-41-7 Structure
IdentificationBack Directory
[Name]

EPZ020411
[CAS]

1700663-41-7
[Synonyms]

CS-2262
EPZ020411
EPZ020411 HCl
EPZ020411 2HCl
EPZ 020411;EPZ-020411
N1,N2-dimethyl-N1-((3-(4-((1r,3r)-3-(2-(tetrahydro-2H-pyran-4-yl)ethoxy)cyclobutoxy)phenyl)-1H-pyrazol-4-yl)methyl)ethane-1,2-diamine
1,2-Ethanediamine, N1,N2-dimethyl-N1-[[3-[4-[[trans-3-[2-(tetrahydro-2H-pyran-4-yl)ethoxy]cyclobutyl]oxy]phenyl]-1H-pyrazol-4-yl]methyl]-
[Molecular Formula]

C25H38N4O3
[MDL Number]

MFCD28963945
[MOL File]

1700663-41-7.mol
[Molecular Weight]

442.59
Chemical PropertiesBack Directory
[Boiling point ]

619.2±55.0 °C(Predicted)
[density ]

1.16±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

crystalline solid
[pka]

14.53±0.50(Predicted)
Hazard InformationBack Directory
[Biological Activity]

epz020411 is an inhibitor of prmt6.prmt6, a member of the protein arginine methyltransferasefamily, comprises 45 enzymes. the post-translational modifications of prmt6 are important regulators of rna processing, transcriptional regulation, and signal transduction.
[in vitro]

in biochemical assays, epz020411 was found to be over 100-fold selective for prmt6/8/1 compared to other histone methyltransferases, such as prmt3, prmt4, prmt5 and prmt7. in addition, epz020411 treatment led to a dose-dependent decrease in h3r2 methylation, while treatment with its prmt6-inactive analog did not generate an ic50 at concentrations up to 20 μm [1].
[in vivo]

animal study found that male sd rats i.v. administered a single dose of epz020411 at 1 mg/kg showed a moderate clearance of 19.7 ml/min/kg, with a volume of distribution at steady state of 11.1 l/kg, and a mean terminal half-life of 8.54 h. following 5 mg/kg s.c. dosing, a good bioavailability of 65.6 was observed, resulting in epz020411 unbound concentration remaining over the prmt6 ic50 for more than 12 h [1].
[IC 50]

10 nm
[storage]

Store at -20°C
[References]

[1] mitchell lh, et al. aryl pyrazoles as potent inhibitors of arginine methyltransferases: identification of the first prmt6 toolcompound. acs med chem lett. 2015 apr 6;6(6):655-659.
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