包装 | 价格(元) |
10mg | 询价 |
50mg | 询价 |
生物活性 | YS-49 (monohydrate) is aPI3K/Akt(a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibitsangiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiacβ-adrenoceptors[1][2][3]. | ||||||||||||||||
IC50& Target | PI3K/Akt[3] | ||||||||||||||||
体外研究 (In Vitro) | YS-49 (1-100 μM; 18 hours; RAVSMC and RAW 264.7 cells) concentration-dependently inhibits the accumulation of nitrite in both RAVSMC and RAW 264.7 exposed to lipopolysaccharide (LPS) plus INF-γ, withIC50values of 22 μM and 30 μM, respectively[2]. Cell Viability Assay[2]
Western Blot Analysis[2]
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体内研究 (In Vivo) | YS-49 (5 mg/kg; intraperitoneal injection; 8 hours; male Sprague Dawley rats) treatment significantly reduces serum NOx levels in LPS-treated rats, the NOx levels reduce from 86 μM to 34 μM[2].
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分子量 | 404.30 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H22BrNO3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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