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. |
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IC50& Target |
IC50: 32.5-42.5 nM (BET)[1] |
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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].
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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].
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Clinical Trial |
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分子量 |
423.90 |
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性状 |
Solid |
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Formula |
C22H22ClN5O2 |
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CAS 号 |
1260907-17-2 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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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)
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In Vivo:
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