BRD7389
產品名稱:BRD7389
產品描述:
產品描述 | BRD7389 is an inhibitor of RSK family kinase with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively. |
靶點活性 | RSK1:1.5 μM, RSK2:2.4 μM, SGK:13.8 μM, PKG1α:6.5 μM, DRAK1:2.8 μM, Pim1:3.7 μM, CDK5/p35:6.5 μM, RSK3:1.2 μM, FLT3:3.5 μM |
體外活性 | BRD7389 (1 μM) almost completely blocked Carbachol (1 mM)-stimulated cell proliferation, but has little effect on the basal level of proliferation[1]. BRD7389 (0.425, 0.85, 1.7, 3.4, 6.8 μM) induces insulin expression in mouse α-cells and induces a dose-dependent up-regulation of insulin (Ins2) mRNA, peaking at 0.85 μM. BRD7389 increases β-cell-specific gene expression in primary human islet cells. BRD7389 (0.85-6.8μM) significantly up-regulates Pdx1 mRNA expression in mouse α-cell line[2]. |
分子量 | 366.41 |
分子式 | C24H18N2O2 |
CAS No. | 376382-11-5 |
存儲
Powder: -20°C for 3 years | In solvent: -80°C for 2 years
溶解度
DMSO: 20 mg/mL (54.58 mM),ultrasonic and warming and heat to 60°C
( < 1 mg/mL refers to the product slightly soluble or insoluble )
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