CAS NO: | 1628830-21-6 |
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 | EZM 2302 is an inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1) with anIC50of 6 nM. | ||||||||||||||||
IC50& Target | IC50: 6 nM (CARM1)[1] | ||||||||||||||||
体外研究 (In Vitro) | EZM 2302 binds to CARM1 and is a selective inhibitor of CARM1 activity (IC50=6 nM) with broad selectivity against other histone methyltransferases. Treatment of MM cell lines with EZM 2302 leads to inhibition of PABP1 and SMB methylation and cell stasis with IC50values in the nanomolar range (9, 31 nM, respectively). EZM 2302 inhibits thein vitroproliferation of multiple hematopoietic cell lines, with day 14 IC50values of less than 100 nM in 9 of 15 cell lines[1]. | ||||||||||||||||
体内研究 (In Vivo) | EZM 2302 is stable in human hepatocytes (CL<3 mL/min/kg), and moderately binds to human, mouse and rat plasma proteins with a mean fraction unbound of 0.66, 0.46 and 0.74, respectively. In mouse and rat, the plasma clearance (CL) is 43 and 91 mL/min/kg, respectively. EZM 2302 shows dose-dependent exposure and tumor growth inhibition (TGI) after 21 days in the RPMI-8226 xenograft model. Tumors in all EZM 2302 dose groups measured on day 21 show significant decreases in tumor growth compared to vehicle[1]. | ||||||||||||||||
分子量 | 585.09 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C29H37ClN6O5 | ||||||||||||||||
CAS 号 | 1628830-21-6 | ||||||||||||||||
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 : 100 mg/mL(170.91 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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