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详细介绍
l 基本信息 |
产品名称 | 艾代拉里斯(Idelalisib) |
一般描述 | Idelalisib(艾代拉里斯)
is Kinase Inhibitor, and Cytochrome P450 3A Inhibitor. |
别 称 | 5-fluoro-3-phenyl-2-[(1S)-1-(7H-purin-6-ylamino)propyl]quinazolin-4-one; CAL-101; GS-1101 |
纯 度 | ≥98%(HPLC) | CAS NO. | 870281-82-6 |
分子式 | C22H18FN7O | 分子量 | 415.432 |
适用范围 | 生物试剂,适用于细胞培养等 |
l 理化信息 |
外 观 | 白色或类白色固体 |
溶解性(25℃) | DMSO | ≥50mg/mL |
乙醇 | ≥20mg/mL |
水 | Insoluble |
l 生物学信息 |
生物活性/药理作用 | Idelalisib is an orally bioavailable, small molecule inhibitor of the delta isoform of the 110 kDa catalytic subunit of class I phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities. Idelalisib inhibits the production of the second messenger phosphatidylinositol-3,4,5-trisphosphate (PIP3), preventing the activation of the PI3K signaling pathway and inhibiting tumor cell
proliferation, motility, and survival. Unlike other isoforms of PI3K, PI3K-delta is expressed primarily in hematopoietic lineages. The targeted
inhibition of PI3K-delta is designed to preserve PI3K signaling in normal, non-neoplastic cells. |
l 包装与存储 |
包 装 | 10mg; 50mg; 250mg |
存储温度 | -20℃ |
l 注意事项及免责声明 |
本产品仅用于实验研究,不得作为药物使用,不得用于家用或其它用途。 |
l 参考文献 |
1. http://www.drugbank.ca 2. https://ncit.nci.nih.gov 3. https://www.ncbi.nlm.nih.gov |