Biological Activity |
NI-57 is an inhibitor of bromodomain and plant homeodomain finger-containing (BRPF) famlily of proteins, with IC50s of 3.1, 46 and 140 nM for BRPF1, BRPF2 (BRD1) and BRPF3, respectively. IC50 & Target: IC50: 3.1 nM (BRPF1), 46 nM (BRPF2 (BRD1)), 140 nM (BRPF3)[1] In Vitro: NI-57 is an inhibitor of bromodomain and plant homeodomain finger-containing (BRPF), with IC50s of 3.1, 46 and 140 nM for BRPF1, BRPF2 (BRD1) and BRPF3, respectively. NI-57 binds the BRD of BRPF1 with a Kd of 31 +/- 2 nM, BRD1 with a Kd of 110 +/- 13 nM, and BRPF3 with a Kd of 410 +/- 47 nM, whereas binding to BRD9 is weaker (Kd 1000 +/- 130 nM) measured by isothermal titration calorimetry. NI-57 shows less active effect on BRD9 (IC50, 520 nM) and BRD4 (BD1) (IC50, 3700 nM), TRIM24 (IC50, 1600 nM). NI-57 also inhibits BRPF BRDs in the nucleus, but shows little effect on the proliferation of many cancer cell lines with GI50s of 10.4 uM (NCI-H1703 cells), 14.7 uM (DMS114), 15.6 uM (HRA-19), and 16.6 uM (RERF-LC-Sq1). Furthermore, Inhibition on BRPF1 of NI-57 (10 uM) reduces the gene expression of CCL-22 by 27.7 +/- 9.4%[1]. In Vivo: NI-57 has favorable oral bioavailability in mice[1]. |