MS023, PRMT Inhibitor
Overview | |
Catalog # | bs-60314c-2-mg-solid |
Product Name | MS023, PRMT Inhibitor |
Specifications | |
Storage Buffer | Powder |
Storage Condition | Store in dry, dark place at -20C for 1 year. |
Target | |
Product Information | Molecular Weight: 287.4 Formula: C17 H25 N3 O CAS Number: 1831110-54-3 InChi Key: FMTVWAGUJRUAKE-UHFFFAOYSA-N InChi: InChI=1S/C17H25N3O/c1-13(2)21-16-6-4-14(5-7-16)17-11-19-10-15(17)12-20(3)9-8-18/h4-7,10-11,13,19H,8-9,12,18H2,1-3H3 Smiles: CC(C)OC1C=CC(=CC=1)C1=CNC=C1CN(C)CCN Purity: 98.0 Solubility: DMSO up to 100 mM; EtOH up to 100 mM Appearance: Solid Power. Shelf Life: 1.0 years |
Description | MS023 is a potent, selective and cell permeable type I PRMT inhibitor (catalyzes mono- and asymmetric dimethylation of arginine residues) with IC50 of 30 nM, 119 nM, 83 nM, 4 nM and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6 and PRMT8, respectively. It is completely inactive against type II and type III PRMTs, protein lysine methyltransferases and DNA methyltransferases. A crystal structure of PRMT6 in complex with MS023 revealed that MS023 binds the substrate binding site. MS023 potently reduces cellular levels of H4R3me2a in MCF7 and HEK293 cells by inhibiting PRMT1/6 methyltransferase activity with IC50 of 9 nM and 56 nM, respectively. It potently decreased cellular levels of histone arginine asymmetric dimethylation. It also reduced global levels of arginine asymmetric dimethylation and concurrently increased levels of arginine monomethylation and symmetric dimethylation in cells. |