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PRGL493为高效、选择性的长链酰基辅酶a合成酶4 (ACSL4) 抑制剂,能在乳腺和前列腺细胞以及动物模型中抑制细胞增殖和肿瘤生长,主要应用于癌症研究。
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PRGL493为高效、选择性的长链酰基辅酶a合成酶4 (ACSL4) 抑制剂,能在乳腺和前列腺细胞以及动物模型中抑制细胞增殖和肿瘤生长,主要应用于癌症研究。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 595 | 现货 | |
5 mg | ¥ 1,290 | 现货 | |
10 mg | ¥ 1,780 | 现货 | |
25 mg | ¥ 2,720 | 现货 | |
50 mg | ¥ 4,580 | 现货 | |
100 mg | ¥ 7,190 | 现货 |
产品描述 | PRGL493 is an inhibitor of long-chain acyl-CoA synthetase 4 (ACSL4).1It inhibits formation of arachidonoyl-CoA (AA-CoA) from arachidonic acid in, as well as the proliferation and migration of, PC3 and MDA-MB-231 cancer cells when used at a concentration of 50 μM. PRGL493 (5 μM) reduces production of progesterone induced by 8-Br-cyclic AMP (8-Br-cAMP) in MA-10 Leydig tumor cells. It inhibits tumor growth in a PC3 mouse xenograft model when administered at a dose of 0.25 mg/kg. |
分子量 | 451.48 |
分子式 | C25H21N7O2 |
CAS No. | 2479378-45-3 |
Smiles | CC(=O)NC1=NC(N2C(Nc3ccccc23)=N1)c1cn(nc1-c1ccc(C)o1)-c1ccccc1 |
存储 | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||
溶解度信息 | Chloroform: 1 mg/mL DMSO: 4.5 mg/mL (10.0 mM), Sonication and heating to 60℃ are recommended. | ||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||
DMSO
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