CAS NO: | 2061980-01-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 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 | XMU-MP-1 is a reversible and selectiveMST1/2inhibitor withIC50s of 71.1 and 38.1 nM, respectively[1]. | ||||||||||||||||
IC50& Target | IC50: 71.1 (MST1), 38.1 nM (MST2)[1] | ||||||||||||||||
体外研究 (In Vitro) | At concentrations ranging from 0.1 to 10 μM, XMU-MP-1 reduces the phosphorylation of endogenous MOB1, LATS1/2, and YAP in HepG2 cells in a dose-dependent manner. XMU-MP-1 treatment inhibits hydrogen peroxide-stimulated MOB1 phosphorylation and MST1/2 autophosphorylation in a variety of cell lines, including mouse macrophage-like cells, human osteosarcoma, human colorectal adenocarcinoma cells. XMU-MP-1 blocks MST1/2 kinase activities, thereby activating the downstream effector Yes-associated protein and promoting cell growth. XMU-MP-1 can potently and reversibly suppress the activities of kinases MST1/2 and enhance their downstream YAP activation in cells[1]. | ||||||||||||||||
体内研究 (In Vivo) | XMU-MP-1 displays excellent inin vivopharmacokinetics and is able to augment mouse intestinal repair, as well as liver repair and regeneration, in both acute and chronic liver injury mouse models at a dose of 1 to 3 mg/kg via intraperitoneal injection. XMUMP-1 treatment exhibits substantially greater repopulation rate of human hepatocytes in the Fah-deficient mouse model than in the vehicle-treated control, indicating that XMU-MP-1 treatment might facilitate human liver regeneration[1]. | ||||||||||||||||
分子量 | 416.48 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H16N6O3S2 | ||||||||||||||||
CAS 号 | 2061980-01-4 | ||||||||||||||||
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 : 8 mg/mL(19.21 mM;Need ultrasonic) 配制储备液
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