Comparison

NI-57

Item no. CS-0015636-100mg
Manufacturer ChemScene
Amount 100mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Similar products 1883548-89-7
Available
CAS
1883548-89-7
Purity
>98%
Formula
C19H17N3O4S
MWt
383.42
Solubility
DMSO : >= 83.3 mg/mL (217.26 mM)
Clinical Information
No Development Reported
Pathway
Epigenetics
Target
Epigenetic Reader Domain
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].

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100mg
Available: In stock
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