selleck产品在文献中的引用: 
    
   
Biochem Biophys   Res Commun, 2013, 437(1):1-6
  
  
   
Cancer Res, 2013, 74(1):298-308
  
  
   
Pharmacol Res, 2014,   10.1016/j.phrs.2014.01.003
  

客户使用selleck产品的实验数据:
 更多详情请访问中国唯一官方网站www.selleck.cn/products/a-769662.html

生物活性
产品描述
A-769662是一种有效的，可逆的AMPK激活剂，EC50为0.8 μM，对GPPase/FBPase活性几乎没有作用效果。
靶点
AMPK
Fatty acid synthesis
 
 
 
 
IC50
0.8 μM
3.2 μM [1]
 
 
 
 
体外研究
A-769662 stimulates partially purified rat liver AMPK with EC50 with 0.8 μM. A-769662 activates AMPK purified from multiple tissues and species in a dose-responsive manner with modest variations in observed EC50s. EC50s determined for A-769662 using partially purified AMPK extracts from rat heart, rat muscle, or human embryonic kidney cells (HEKs) are 2.2 mM, 1.9 mM, or 1.1 mM, respectively. A 4 hours treatment of primary rat hepatocytes with A-769662 dose-dependently increases ACC phosphorylation, which correlated inhibition of fatty acid synthesis with IC50 of 3.2 μM. A-769662 also inhibits fatty acid sythesis in mouse hepatocytes with IC50 with 3.6 μM [1] A-769662 activates AMPK both allosterically and by inhibiting dephosphorylation of AMPK on Thr-172, similar to the effects of AMP. [2] A-769662 inhibits proteasomal function by an AMPK-independent mechanism. A-769662 affects the in vitro activity of purified 26S proteasomes but not the in vitro activity of purified 20S proteasomes. A-769662 has toxic effects on MEF cells. [3] A recent research shows A-769662 inhibited cell proliferation and DNA synthesis. [4]
体内研究
Short-term treatment of normal Sprague Dawley rats with A-769662 decreases liver malonyl CoA levels and the respiratory exchange ratio, VCO2/VO2, indicating an increased rate of whole-body fatty acid oxidation. Treatment of ob/ob mice with 30 mg/kg b.i.d. A-769662 decreases hepatic expression of PEPCK, G6Pase, and FAS, lowers plasma glucose by 40%, reduced body weight gain and significantly decreases both plasma and liver triglyceride levels. [1]
特征
 
推荐的实验操作(此推荐来自于公开的文献所以Selleck并不保证其有效性)
激酶实验: 
[1]
96-well AMPK assay
AMPK activity is measured by monitoring phosphorylation of the SAMS peptide substrate (20 mM in standard assays and 100 mM in additivity assays) following a previously described protocol (Anderson et al., 2004). To determine whether A-769662-induced AMPK activation occurs in a reversible manner, AMP or A-769662 are preincubated with rat liver AMPK for 10 minutes at 20 times standard assay concentrations prior to dilution and measurement of AMPK activity.
Fatty Acid Synthesis Assay
Primary rat hepatocytes are isolated and plated at 5 × 104 cells per well on BioCoat, collagen-coated, black-walled 96-well plates in DMEM supplemented with 10% FBS, 5 mM glucose, 1 mM sodium pyruvate, 2 mM L-glutamine, 25 mM HEPES, 0.1 mM nonessential amino acids, 5 mg/mL ransferring, 100 nM dexamethasone, 100 nM insulin and 25 mg/mL gentamycin. After 4 hours medium is replaced with medium but without FBS and containing 100 nM triiodothyronine (T3). Following a 16 hours, 37 °C incubation, the incubation medium is removed and replaced with medium containing 14C acetate (2 mCi/mL) and Acadesine at the indicated concentrations. Cells are incubated 4 hours at 37 °C then the plates are rinsed with PBS. The final wash is replaced with Microscint20 and radioactivity incorporate into fatty acid monitored on a Wallac Microbeta plate rea
细胞试验: 
[3]
细胞系
MEF cells
浓度
300 μM
处理时间
24 hours
方法
Cell viability of MEF cells treated or not with A-769662 is performed as follows: cells are harvested by trypsinization and incubated with 0.5 mg/mL RNase and 50 μg/mL propidium iodine at room temperature in the dark; cell viability is analyzed by flow cytometry using a FACScanto flow cytometer, using an excitation laser at 488 nm and a propidium iodine fluorescence detection at 600 nm. To determine the proportion of cells in each phase of the cell cycle, cells are harvested by trypsinization, collected by centrifugation, washed in PBS and fixed overnight in 80% ethanol at -20 °C. Subsequently, these fixed cells are centrifuged to remove the fixative and incubated for 20 minutes in the dark at room temperature in PBS containing 0.5 mg/mL RNase and 50 μg/mL propidium iodine. Flow cytometry analysis is performed as above. The proportion of cells in G1, S, and G2 is determined using the MODFIT program. Cell culture pictures are taken at the indicated times using a camera coupled to an inverted microscope with a 20 × objective.
动物实验: 
[1]
动物模型
Sprague Dawley rats
配制
A-769662 is dissolved in DMSO.
剂量
30 mg/kg
给药处理
Administered via i.p.
溶解度
1% DMSO/30% polyethylene glycol/1% Tween 80, 30 mg/mL
参考文献
[1] Cool B, et al, Cell Metab, 2006, 3(6), 403-416.
[2] Sanders MJ, J Biol Chem, 2007, 282(45), 32539-32548.
[3] Moreno D, et al, FEBS Lett, 2008, 583(17), 2650-2654.
[4] Pevton KJ, et al, J Pharmacol Exp Ther, 2012, Jun 13.