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BJJF078 是一种氨基哌啶衍生物,是一种有效的重组人和小鼠谷氨酰胺转氨酶 (TG2) 活性的抑制剂,对人和小鼠谷氨酰胺转氨酶的IC50 值分别为 41 和 54 nM。BJJF078 对 TG1 酶有抑制作用,其IC50 为 0.16 μM。 BJJF078 可用于研究多发性硬化症 (MS) 。
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BJJF078 是一种氨基哌啶衍生物,是一种有效的重组人和小鼠谷氨酰胺转氨酶 (TG2) 活性的抑制剂,对人和小鼠谷氨酰胺转氨酶的IC50 值分别为 41 和 54 nM。BJJF078 对 TG1 酶有抑制作用,其IC50 为 0.16 μM。 BJJF078 可用于研究多发性硬化症 (MS) 。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 347 | In stock | |
5 mg | ¥ 765 | In stock | |
10 mg | ¥ 1,090 | In stock | |
25 mg | ¥ 1,850 | In stock | |
50 mg | ¥ 2,750 | In stock | |
100 mg | ¥ 3,970 | In stock | |
200 mg | ¥ 5,790 | In stock |
BJJF078 相关产品
产品描述 | BJJF078, an aminopiperidine derivative, is a potent inhibitor of recombinant human and mouse glutamine aminotransferase (TG2) activity, with IC50 values of 41 and 54 nM for human and mouse glutamine aminotransferase, respectively.BJJF078 inhibits TG1 enzyme, with an IC50 of 0.16 μM.BJJF078 can be used to study multiple sclerosis (MS). BJJF078 can be used to study multiple sclerosis (MS). |
靶点活性 | TGase 1:0.16 μM, TG2 (human):41 nM, TG2 (mouse):54 nM |
分子量 | 523.6 |
分子式 | C27H29N3O6S |
CAS No. | 2531244-56-9 |
Smiles | S(=O)(=O)(C=1C2=C(C(NC(=O)C3=CC(OC)=C(OC)C=C3)=CC=C2)C=CC1)N4CCC(NC(C=C)=O)CC4 |
密度 | 1.36 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 60 mg/mL (114.59 mM), Sonication is recommended. ![]() | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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