CAS NO: | 1260907-17-2 |
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 |
1 g | 电议 |
生物活性 | Molibresib (I-BET762; GSK525762) is aBET bromodomaininhibitor withIC50of 32.5-42.5 nM. | ||||||||||||||||
IC50& Target | IC50: 32.5-42.5 nM (BET)[1] | ||||||||||||||||
体外研究 (In Vitro) | Molibresib (I-BET 762) shows the highest affinity interaction with BET. Molibresib binds to the tandem bromodomains of BET with high affinity (dissociation constant Kdof 50.5-61.3 nM). Molibresib displaces, with high efficacy (half-maximum inhibitory concentration IC50of 32.5-42.5 nM), a tetra-acetylated H4 peptide that had been pre-bound to tandem bromodomains of BET[1]. Molibresib has high affinity for BD1/BD2 domain of BRD2/3/4 proteins. Molibresib treatment leads to a reduction in the recruitment of all three proteins to chromatin[2]. Molibresib inhibits OPM-2 cell proliferation with IC50of 60.15 nM[3]. | ||||||||||||||||
体内研究 (In Vivo) | The antimyeloma activity of Molibresib (I-BET 762) is tested dosed orally in an in vivo systemic xenograft model generated by injecting OPM-2 cells into NOD-SCID mice. Daily oral doses of Molibresib up to 10 mg/kg and 30 mg/kg given every other day are well tolerated with no clear impact on body weight compared with vehicle control. The plasma hLC concentration is significantly reduced in mice treated with Molibresib[3]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 423.90 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H22ClN5O2 | ||||||||||||||||
CAS 号 | 1260907-17-2 | ||||||||||||||||
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 : 200 mg/mL(471.81 mM;Need ultrasonic) 1M HCl : 100 mg/mL(235.90 mM;ultrasonic and adjust pH to 1 with HCl) 配制储备液
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以下溶剂前显示的百
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