CAS NO: | 1196541-47-5 |
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 |
GDC-0575 (ARRY-575, RG7741) is a highly-selective oral small-moleculeChk1inhibitor with anIC50of 1.2 nM. |
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IC50& Target |
1.2 nM (Chk1)[1] |
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体外研究 (In Vitro) |
GDC-0575 is significantly more potent in promoting DNA damage, replication stress and cell death than V158411, LY2603618, and MK-8776 in a panel of melanoma cell lines[1]. GDC-0575 abrogates DNA damage-induced S and G2–M checkpoints, exacerbates DNA double-strand breaks and induces apoptosis in STS cells. GDC-0575 has a synergistic or additive effect together with gemcitabine[2]. CHK1 inhibitor GDC-0575 in combination with AraC enhances the killing of primary acute myeloid leukemia cellsex vivoby inducing apoptosis[3].
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体内研究 (In Vivo) |
GDC-0575 is active at 25 mg/kg as a single agent, but the efficacy is improved at the higher drug dose. GDC-0575 effectively blocks tumor growth in the D20 and C002 xenografts, and the effect is maintained for at least 10 days after the final dose is administered[1].
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Clinical Trial |
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分子量 |
378.27 |
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性状 |
Solid |
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Formula |
C16H20BrN5O |
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CAS 号 |
1196541-47-5 |
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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 : 100 mg/mL(264.36 mM;Need ultrasonic) H2O :< 0.1 mg/mL(insoluble)
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