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PI3Kδ-IN-21 (Compound 31) 是一种选择性抑制磷酸肌醇 3-激酶 δ (PI3Kδ) 的抑制剂,具有13.6 nM的IC50。它通过PI3K/AKT/mTOR信号通路抑制T细胞的增殖与分化。在大鼠模型中,PI3Kδ-IN-21展现出优良的药代动力学特性,并在髓磷脂少突胶质细胞糖蛋白 (MOG) 诱导的实验性自身免疫性脑脊髓炎(EAE)模型中显示改善的活性。
PI3Kδ-IN-21 (Compound 31) 是一种选择性抑制磷酸肌醇 3-激酶 δ (PI3Kδ) 的抑制剂,具有13.6 nM的IC50。它通过PI3K/AKT/mTOR信号通路抑制T细胞的增殖与分化。在大鼠模型中,PI3Kδ-IN-21展现出优良的药代动力学特性,并在髓磷脂少突胶质细胞糖蛋白 (MOG) 诱导的实验性自身免疫性脑脊髓炎(EAE)模型中显示改善的活性。

PI3Kδ-IN-21 相关产品
| 产品描述 | PI3Kδ-IN-21 (Compound 31) is a selective inhibitor of phosphoinositide 3-kinase δ (PI3Kδ), with an IC50 of 13.6 nM. It impedes the proliferation and differentiation of T cells through the PI3K/AKT/mTOR signaling pathway. In rat models, PI3Kδ-IN-21 exhibits favorable pharmacokinetic properties and demonstrates activity in improving experimental autoimmune encephalomyelitis induced by myelin oligodendrocyte glycoprotein (MOG) in EAE models. |
| 靶点活性 | PI3Kδ:13.6 nM, PI3Kα:7034 nM, PI3Kβ:1660 nM |
| 分子式 | C19H16ClN9 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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