CAS NO: | 1454808-95-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | LP-922761 is a potent, selective and orally activeadapter protein-2 associated kinase 1 (AAK1) inhibitor withIC50s of 4.8 nM and 7.6 nM in enzyme and cell assays, respectively. LP-922761 also inhibitsBMP-2-inducible protein kinase (BIKE)with anIC50of 24 nM. LP-922761 exhibits no significant activity atcyclin G-associated kinase (GAK), opioid, adrenergic α2 or GABAa receptors[1]. | ||||||||||||||||
IC50& Target | IC50: 4.8 nM (Adapter protein-2 associated kinase 1 (AAK1) in enzyme assays); 7.6 nM (AAK1 in cell assays); 24 nM (BMP-2-inducible protein kinase (BIKE))[1] | ||||||||||||||||
体内研究 (In Vivo) | In mouse, LP-922761 has a brain to plasma ratio of 0.007, indicating that LP-922761 is essentially restricted to the peripheral compartment[1]. | ||||||||||||||||
分子量 | 410.47 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H26N6O3 | ||||||||||||||||
CAS 号 | 1454808-95-7 | ||||||||||||||||
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 : 41.67 mg/mL(101.52 mM;ultrasonic and warming and heat to 80℃) 配制储备液
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