產品屬性:
產品名稱 | ML-9 |
規格 | 10 mg、50 mg、100 mg、250 mg |
貨號 | EY-01Y16789 |
Cas No.: 4870
別名: N/A
化學名: N/A
分子式: C15H17ClN2O2S·HCl

分子量: 361.3
溶解度: DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2)(1:1): 0.5 mg/ml,Ethanol: 0.5 mg/ml
儲存條件: -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
產品描述:
ML-9 was originally identified as a selective Ca2+-calmodulin-dependent myosin light chain kinase inhibitor. Concentrations from 10-100 μM are effective at inhibiting vascular smooth muscle tension and reducing intracellular Ca2+ concentrations.1 ML-9 also inhibits PKB/Akt activity with an IC50 range of 10-50 μM in rat primary adipocytes. This results in a specific inhibition of insulin-stimulated glucose transport and GLUT4/IGF II receptor translocation to the plasma membrane yet does not interfere with the antilipolytic effect of insulin.2 Additionally, ML-9 inhibits other serine/threonine kinases including PKA (IC50 = ~20 μM), p90 S6 (IC50 = ~50 μM), and MAP kinase (IC50 = ~35 μM).21.Ito, S., Kume, H., Honjo, H., et al.ML-9, a myosin light chain kinase inhibitor, reduces intracellular Ca2+ concentration in guinea pig trachealisEuropean Journal of Pharmacology486325-333(2004)
2.Smith, U., Carvalho, E., Mosialou, E., et al.PKB inhibition prevents the stimulatory effect of insulin on glucose transport and protein translocation but not the antilipolytic effect in rat adipocytesBiochemical and Biophysical Research Communications268315-320(2000)
特別提醒公司產品僅供科研使用