CAS NO: | 1627091-47-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | MLi-2 is an orally active and highly selectiveLRRK2inhibitor with anIC50of 0.76 nM. MLi-2 has the potential for Parkinson’s disease[1]. | ||||||||||||||||
IC50& Target | IC50: 0.76 nM (LRRK2)[1] | ||||||||||||||||
体外研究 (In Vitro) | MLi-2 exhibits exceptional potency in a purified LRRK2 kinase assayin vitro( IC50=0.76 nM), a cellular assay monitoring dephosphorylation of LRRK2 pSer935 LRRK2 (IC50=1.4 nM), and a radioligand competition binding assay (IC50=3.4 nM). MLi-2 has greater than 295-fold selectivity for over 300 kinases in addition to a diverse panel of receptors and ion channels[1]. | ||||||||||||||||
体内研究 (In Vivo) | Acute oral and subchronic dosing in MLi-2 mice results in dose-dependent central and peripheral target inhibition over a 24-hour period as measured by dephosphorylation of pSer935 LRRK2. Treatment of MitoPark mice with MLi-2 is well tolerated over a 15-week period at brain and plasma exposures. Morphologic changes in the lung, consistent with enlarged type II pneumocytes, are observed in MLi-2-treated MitoPark mice[1]. | ||||||||||||||||
分子量 | 379.46 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H25N5O2 | ||||||||||||||||
CAS 号 | 1627091-47-7 | ||||||||||||||||
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 : 50 mg/mL(131.77 mM;Need ultrasonic) 配制储备液
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