125256-00-0
                            中文名称
                            FATOSTATIN A
                        
                        
                            英文名称
                            Fatostatin A
                        
                        
                            CAS
                            125256-00-0
                        
                        
                            分子式
                            C18H18N2S
                        
                        
                            分子量
                            294.41
                        
                        
                            MOL 文件
                            125256-00-0.mol
                        
                        
                            更新日期
                            2025/10/13 11:49:06
                        
                    
                        125256-00-0 结构式
                    基本信息
中文别名
脂肪抑制素  英文别名
125B11Pyridine, 4-[4-(4-methylphenyl)-2-thiazolyl]-2-propyl-
4-(4-methylphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole
物理化学性质
沸点474.3±55.0 °C(Predicted)
密度1.125±0.06 g/cm3(Predicted)
储存条件Inert atmosphere,2-8°C
溶解度溶于 DMSO(高达 25 mg/ml)。
酸度系数(pKa)3.46±0.10(Predicted)
形态固体
颜色黄色
稳定性DMSO中的溶液可在-20°下稳定储存3个月。
FATOSTATIN A价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 | 
| 2025/09/19 | S9785 | FATOSTATIN A Fatostatin  | 125256-00-0 | 5mg | 795.2元 | 
| 2025/09/19 | S9785 | Fatostatin | 125256-00-0 | 10mM (1mL in DMSO) | 958.23元 | 
| 2025/09/19 | S9785 | FATOSTATIN A Fatostatin  | 125256-00-0 | 25mg | 2375.39元 | 
常见问题列表
生物活性
Fatostatin (125B11) 是一种diarylthiazole的衍生物,是 Sterol regulatory element binding proteins (SREBPs) 活化的特异性抑制剂。Fatostatin 可结合SCAP (SREBP cleavage-activating protein),并抑制SREBP的ER-Golgi易位。Fatostatin 可抑制癌细胞生长并增强癌细胞的凋亡。靶点
| Target | Value | 
| 
 SREBP
  ()  | 
体外研究
  Fatostatin (125B11) (0.1-1 μM; 3 days) inhibits the androgen-independent prostate cancer cell proliferation (IC
  
   50
  
  =0.1 μM) in an independent of the known IGF1-signaling pathway. Fatostatin inhibits insulin-induced adipogenesis of 3T3-L1 cells.
  
  Fatostatin directly binds SCAP and blocks its ER-to-Golgi transport with IC
  
   50
  
  of 2.5 and 10 μM in mammalian cells.
 
Cell Proliferation Assay
| Cell Line: | DU-145 cells | 
| Concentration: | 0.1, 1 μM | 
| Incubation Time: | 3 days | 
| Result: | Impaired the IGF1-induced growth at an IC 50 of 0.1 μM. | 
体内研究
Fatostatin (125B11) (30 mg/kg; 150 μL; i.p. injection; daily for 28 days) reduces adiposity, ameliorated fatty liver by reducing triglyceride (TG) storage, and lowered hyperglycemia in ob/ob mice.
| Animal Model: | Four-to-five-week-old homozygous male obese ( ob/ob ) mice (C57BL/6J) | 
| Dosage: | 30 mg/kg; 150 μL | 
| Administration: | i.p. injection; daily for 28 days | 
| Result: | Blocked increases in body weight, blood glucose, and hepatic fat accumulation in obese ob/ob mice, even under uncontrolled food intake. | 
