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376382-11-5

376382-11-5 Structure

376382-11-5 Structure
IdentificationBack 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 PropertiesBack 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.
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack 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
Spectrum DetailBack Directory
[Spectrum Detail]

1-[(2-Phenylethyl)amino]-3H-naphtho[1,2,3-de]quinoline-2,7-dione(376382-11-5)1HNMR
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