CAS NO: | 1927857-61-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | PQR530 is a potent, ATP-competitive, orally bioavailable and brain-penetrant dual pan-PI3K/mTORC1/2inhibitor, with a subnanomolarKdtowardPI3KαandmTOR(0.84 and 0.33 nM, respectively). Antitumor activity[1][2]. | ||||||||||||||||
IC50& Target[2] |
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体外研究 (In Vitro) | PQR-530 is a potent, oral and brain-penetrant dual pan-PI3K/mTORC1/2 inhibitor, exhibiting antitumor activity. PQR-530 inhibits all PI3K isoforms and mTOR complexes C1/2 potently and selectively. PQR-530 inhibits protein kinase B (PKB, pSer473) and ribosomal protein S6 (pS6, pSer235/236) phosphorylation with IC50values of 0.07 μM in A2058 melanoma cells. PQR-530 shows inhibitory activity against the growth of 44 cancer cell lines with mean GI50of 426 nM[1]. | ||||||||||||||||
分子量 | 407.42 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H23F2N7O2 | ||||||||||||||||
CAS 号 | 1927857-61-1 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(81.81 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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