| | Identification | Back Directory |  | [Name] 
 1-[(2-Phenylethyl)amino]-3H-naphtho[1,2,3-de]quinoline-2,7-dione
 |  | [CAS] 
 376382-11-5
 |  | [Synonyms] 
 BRD 7389
 BRD 7389
(BRD7389)
 BRD7389 >=98% (HPLC)
 Insulin Expression Inducer, BRD7389
 1-Phenethylamino-3H-naphtho[1,2,3-de]quinoline-2,7-dione
 1-[(2-Phenylethyl)amino]-3H-naphtho[1,2,3-de]quinoline-2,7-dione
 1-[(2-Phenylethyl)amino]-naphtho-3H-[1,2,3-de]quinoline-2,7-dione
 Insulin Expression Inducer, BRD7389 - CAS 376382-11-5 - Calbiochem
 3H-Naphtho[1,2,3-de]quinoline-2,7-dione, 1-[(2-phenylethyl)aMino]-
 |  | [Molecular Formula] 
 C24H18N2O2
 |  | [MDL Number] 
 MFCD02924820
 |  | [MOL File] 
 376382-11-5.mol
 |  | [Molecular Weight] 
 366.41
 | 
 | Chemical Properties | Back Directory |  | [Boiling point ] 
 655.0±55.0 °C(Predicted)
 |  | [density ] 
 1.35±0.1 g/cm3(Predicted)
 |  | [storage temp. ] 
 Store at +4°C
 |  | [solubility ] 
 DMSO: >20mg/mL
 |  | [form ] 
 powder
 |  | [pka] 
 11.31±0.40(Predicted)
 |  | [color ] 
 orange
 |  | [Stability:] 
 Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
 | 
 | Hazard Information | Back Directory |  | [Description] 
 BRD7389 is an inhibitor of ribosomal S6 kinases (RSKs; IC50s = 1.5, 2.4, and 1.2 μM for RSK1, RSK2, and RSK3, respectively). Through this action, BRD7389 causes mouse αTC1 pancreatic α cells to adopt several morphological and gene expression features of β cells, including increased insulin expression. BRD7389 also enhances glucose-stimulated insulin and glucagon secretion by pancreatic islet cells isolated from human donors with a low body mass index.
 |  | [Uses] 
 BRD7389 is a specific RSK family kinase inhibitor with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively. BRD7389 is a small-molecule inducer of insulin expression in pancreatic α-cells[1].
 |  | [Definition] 
 ChEBI: LSM-4550 is a member of anthracenes.
 |  | [IC 50] 
 RSK1: 1.5 μM (IC50); RSK2: 2.4 μM (IC50); RSK3: 1.2 μM (IC50); CDK5/p35: 6.5 μM (IC50); DRAK1: 2.8 μM (IC50); FLT3: 3.5 μM (IC50); PIM1: 3.7 μM (IC50); PKG1α: 6.5 μM (IC50); SGK: 13.8 μM (IC50)
 |  | [storage] 
 Store at -20°C
 |  | [References] 
 1) Fomina-Yadlin et al. (2010), Small molecule inducers of insulin expression in pancreatic alpha-cells; Proc. Natl. Acad. Sci. USA, 107 15099
2) Choudhary et al. (2014), Quantitative-proteomic comparison of alpha and Beta cells to uncover novel targets for lineage reprogramming; PLoS One, 9(4) e95194
3) Park and Cho (2012), EGFR and PKC are involved in the activation of ERK1/2 and p90 RSK and the subsequent proliferation of SNU-470 colon cancer cells by muscarinic acetylcholine receptors; Mol. Cell. Biochem., 370 191
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