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Size | Price | Stock |
---|---|---|
10mg | $350 | 3-6 Days |
25mg | $600 | 3-6 Days |
50mg | $1050 | 3-6 Days |
100mg | $1750 | 3-6 Days |
250mg | $2550 | 3-6 Days |
Cat #: V20664 CAS #: 2095432-47-4 Purity ≥ 99%
Description: EPZ-020411 (EPZ020411) 2HCl, the dihydrochloride salt of EPZ-020411, is a novel, potent and selective inhibitor of PRMT6 (protein arginine methyltransferase) with the potential to be used for cancer treatment. It inhibits PRMT6 with an IC50 value of 10 nM.
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Molecular Weight (MW) | 515.52 |
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Molecular Formula | C25H40Cl2N4O3 |
CAS No. | 2095432-47-4 |
Synonyms | EPZ020411 HCl; EPZ020411; EPZ 020411; EPZ-020411; EPZ020411 hydrochloride |
Protocol | In Vitro | In vitro activity: Treatment with EPZ020411 results in a dose-dependent decrease in H3R2 methylation in A375 human melanoma cells exogenously overexpressing PRMT6(IC50=0.637±0.241 μM). In biochemical assays EPZ020411 is over 100-fold selective for PRMT6/8/1 compared to other histone methyltransferases including four arginine methyltransferases (PRMT3, PRMT4, PRMT5, and PRMT7). The compound shows poor permeability in the parallel artificial membrane permeation assay. Kinase Assay: EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has >10 fold selectivity for PRMT6 over PRMT1 and PRMT8. Cell Assay: A375 (CRL-1619) cells are cultured in DMEM plus 10% (vol/vol) FBS. PRMT6 is cloned into BamHI and EcoRI sites of a pcDNA4 HisMAX_A plasmid. Transfection of his-tagged PRMT6 or vector control is carried out using Lipofectamine LTX and Plus reagent according to procedures recommended by the manufacturer. Cells are seeded at 200,000 cells/well in 6-well plates. The following day, the cells are concurrently transfected and treated with compound in 0.25% DMSO. Cells are incubated in the presence of increasing concentrations of compound up to 20 μM. Cell pellets are collected after 48 hours of compound treatment. |
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In Vivo | EPZ020411 shows good bioavailability following subcutaneous dosing in rats making it a suitable tool for in vivo studies. Male Sprague-Dawley rats administered a single dose of EPZ020411 at 1 mg/kg by i.v. bolus show a moderate clearance (CL) of 19.7±1.0 mL/min/kg, with a volume of distribution at steady state (Vss) of 11.1±1.6 L/kg, translating to a mean terminal half-life (t1/2) of 8.54±1.43 h. Following 5 mg/kg s.c. dosing, a good bioavailability of 65.6 ± 4.3% is observed, leading to EPZ020411 unbound blood concentration remaining above the PRMT6 biochemical IC50 value for more than 12 h. | |
Animal model | Sprague-Dawley rats |
Solvent volume to be added | Mass (the weight of a compound) | |||
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Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 1.9398 mL | 9.6989 mL | 19.3979 mL | 38.7958 mL |
5mM | 0.3880 mL | 1.9398 mL | 3.8796 mL | 7.7592 mL |
10mM | 0.1940 mL | 0.9699 mL | 1.9398 mL | 3.8796 mL |
20mM | 0.0970 mL | 0.4849 mL | 0.9699 mL | 1.9398 mL |
This equation is commonly abbreviated as: C1 V1 = C2 V2
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.