Powder: -20°C for 3 years
In solvent: -80°C for 2 years
YS-49 is an activator of PI3K/Akt (a downstream target of RhoA).
Description | YS-49 is an activator of PI3K/Akt (a downstream target of RhoA). |
In vitro | In RAVSMC and RAW 264.7 cells, YS-49 (1-100?μM; 18 hours; ) concentration-dependently inhibits the accumulation of nitrite in both RAVSMC and RAW 264.7 exposed to lipopolysaccharide (LPS) plus INF-γ, with IC50 values of 22 μM and 30?μM, respectively[2].At the transcriptional level, YS-49 (10-100?μM; 18 hours; RAVSMC and RAW 264.7 cells) suppresses iNOS gene expression induced by LPS and/or cytokines in RAVSMC and RAW 264.7 cells [2]. |
In vivo | In male Sprague Dawley rats,YS-49 (5?mg/kg; intraperitoneal injection; 8 hours) treatment significantly reduces serum NOx levels in LPS-treated rats, the NOx levels reduce from 86 μM to 34 μM[2]. |
Molecular Weight | 386.28 |
Formula | C20H20BrNO2 |
CAS No. | 132836-42-1 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
H2O: 10 mg/mL (25.89 mM), ultrasonic and warming and heat to 60°C
DMSO: 100 mg/mL (258.88 mM)
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
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YS-49 132836-42-1 Cytoskeletal Signaling Endocrinology/Hormones GPCR/G Protein Neuroscience PI3K/Akt/mTOR signaling Adrenergic Receptor RAAS PI3K Akt inhibit Phosphoinositide 3-kinase PKB Beta Receptor YS 49 Protein kinase B Inhibitor YS49 Angiotensin Receptor inhibitor