7
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T38421 | PRMT1-IN-1 | PRMT1-IN-1 | |
PRMT1-IN-1 is a PRMT1 inhibitor. | |||
T10682L | CARM1-IN-1 | CARM1-IN-7G | Histone Methyltransferase |
CARM1-IN-1 (CARM1-IN-7G) is a selective inhibitor of CARM1 with IC50 of 8.6 μM. CARM1-IN-1 shows weak activity against PRMT1 and SET7 with IC50 > 600 μM. | |||
T27133 | DCLX069 | DCLX 069,DCLX-069 | Histone Methyltransferase |
DCLX069 is a potent and selective PRMT1 inhibitor. DCLX069 occupies the SAM binding pocket to exert the inhibitory effect. DCLX069 effectively blocks cell proliferation in breast cancer, liver cancer and acute myeloid le... | |||
T64186 | CARM1-IN-1 hydrochloride | ||
CARM1-IN-1 hydrochloride is a potent and selective inhibitor of CARM1 (IC50: 8.6 μM) with low inhibition of PRMT1 and SET7. | |||
T27395 | Furamidine dihydrochloride | DB 75, DB75, NSC 305831, WR199385,Furamidine HCl | |
Furamidine is a cell-permeable, selective inhibitor of protein arginine methyltransferase 1 (PRMT1). Furamidine binds to strings of AT base pair sequences in DNA′s minor groove. Furamidine targets the enzyme active site ... | |||
T81399 | PRMT4-IN-2 | ||
PRMT4-IN-2 (compound 55) acts as a pan-inhibitor across various protein arginine methyltransferase (PRMT) isoforms, exhibiting inhibitory potencies with IC50 values of 92 nM for PRMT4, 436 nM for PRMT6, 460 nM for PRMT1,... | |||
T36802 | Bisubstrate Inhibitor 78 | ||
Bisubstrate inhibitor 78 is an inhibitor of nicotinamide N-methyltransferase (NNMT; IC50= 1.41 μM).1It binds the NNMT active site in the binding pockets for the NNMT substrates S-adenosyl-L-methionine (SAM) and nicotinam... |