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CPDA 是新型 SH2 domain-containing inositol phosphatase 2 抑制剂,能够作用于3T3-L1脂肪细胞,改善胰岛素抗性。
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CPDA 是新型 SH2 domain-containing inositol phosphatase 2 抑制剂,能够作用于3T3-L1脂肪细胞,改善胰岛素抗性。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 298 | In stock | |
5 mg | ¥ 690 | In stock | |
10 mg | ¥ 1,160 | In stock | |
25 mg | ¥ 2,170 | In stock | |
50 mg | ¥ 3,480 | In stock | |
100 mg | ¥ 4,960 | In stock | |
200 mg | ¥ 6,860 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 588 | In stock |
CPDA 相关产品
产品描述 | CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2). |
体外活性 | CPDA enhances insulin signaling. CPDA was found to enhance in vitro insulin signaling through the Akt pathway more efficiently than the previously reported SHIP2 inhibitor AS1949490, and ameliorated abnormal glucose metabolism in diabetic (db/db) mice. |
体内活性 | CPDA greatly improves abnormal glucose metabolism in diabetic animals. In db/db mice, CPDA improves abnormal glucose metabolism. |
分子量 | 388.8 |
分子式 | C20H15ClF2N2O2 |
CAS No. | 1415834-63-7 |
Smiles | Fc1cccc(F)c1CC(=O)Nc1cc(OCc2ccc(Cl)cc2)ccn1 |
密度 | 1.381 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: 50 mg/mL (128.6 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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