BAY K 8644 206 UNC0638 inhibits H3K9 dimethylation in

UNC0638 inhibits H3K9 dimethylation in MDA-MB231 cells with an IC50 of 81 nM

an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models

inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of bacteria

CID 2011756 was the most potent of the inhibitors with a cellular EC50 of 10±0

BAY K 8644 206 UNC0638 inhibits H3K9 dimethylation inBay K 8644 is a potent selective activator of L type Ca2 channel with IC50 of 173 nM Product information CAS Number: 71145 03 4 Molecular Weight: 356. 30 Formula: C16H15F3N2O4 Chemical Name: methyl 2,6 dimethyl 5 nitro 4 [2 (trifluoromethyl)phenyl] 1,4 dihydropyridine 3 carboxylate Smiles: COC(=O)C1C(C(=C(C)NC=1C)[N+]([O ])=O)C1=CC=CC=C1C(F)(F)F InChiKey: ZFLWDHHVRRZMEI UHFFFAOYSA N InChi: InChI=1S C16H15F3N2O4 c1 8 12(15(22)25 3)13(14(21(23)24)9(2)20