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RGX-202 (β-GPA) 是口服有活性的SLC6A8转运蛋白抑制剂。它在体内外均能够强烈地抑制肌酸输入,降低细胞内磷酸肌酸和 ATP 水平,诱导肿瘤凋亡,可于研究肿瘤。
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RGX-202 (β-GPA) 是口服有活性的SLC6A8转运蛋白抑制剂。它在体内外均能够强烈地抑制肌酸输入,降低细胞内磷酸肌酸和 ATP 水平,诱导肿瘤凋亡,可于研究肿瘤。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥ 108 | 现货 | |
10 mg | ¥ 137 | 现货 | |
25 mg | ¥ 198 | 现货 | |
50 mg | ¥ 282 | 现货 | |
100 mg | ¥ 428 | 现货 | |
200 mg | ¥ 625 | 现货 | |
500 mg | ¥ 987 | 现货 | |
1 g | ¥ 1,450 | 现货 |
产品描述 | RGX-202 (β-GPA) is a creatine analog that alters skeletal muscle energy expenditure. It reduces cellular ATP, creatine, and phosphocreatine levels and stimulates AMP-activated protein kinase (AMPK), activating PPARγ coactivator 1α (PGC-1α). |
体外活性 | 3-Guanidinopropionic acid促使代谢从糖酵解向氧化代谢转变, 增加细胞对葡萄糖的摄取,并提高了疲劳耐受性[1]。 |
体内活性 | 3-Guanidinopropionic Acid(β-GPA) 降低了β-氧化基因的表达。在小鼠体内使用β-GPA 3周显著增强了动物的体力和耐力健康,即提高了它们的体力和耐力,并减轻了焦虑。β-GPA可能被视为一种对哺乳动物的肌肉和大脑代谢均有影响的适应原[2]。 |
动物实验 | The following animal groups were used for the experiment: (1) mice that were not subjected to injections (n = 10)—this group was used only for physiological tests and were not killed after the experiment;?(2) saline-treated mice (n = 8)—the volume of injections was 200 μL;?and (3) β-GPA-treated mice (n = 8)—concentration of β-GPA was 1 mg/kg/day.?The volume of injections was 200 μL.Injections were performed 3 times a week for 3 weeks.?The mice's weight and the total amount of consumed food and water were measured daily.?Once a week, a string test was performed.?Measurements of the oxygen consumption rates of live animals and the open field test were performed after the course of injections.?After 3 weeks, the mice were killed;?brain dissection was performed to extract the cortex and the ventral midbrain (VMB) for quantitative real-time polymerase chain reaction (qRT-PCR) analysis[2]. |
别名 | 胍基丙酸, β-GPA, 3-Guanidinopropionic Acid |
分子量 | 131.13 |
分子式 | C4H9N3O2 |
CAS No. | 353-09-3 |
Smiles | C(CC(O)=O)NC(=N)N |
密度 | 1.46 g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度信息 | DMSO: Slightly soluble |
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