GDC-0575
CAS No. 1196541-47-5
GDC-0575 ( ARRY-575 | RG-7741 | GDC0575 )
产品货号. M10694 CAS No. 1196541-47-5
GDC-0575 (ARRY-575, RG-7741) 是一种有效的、选择性的、口服生物可利用的 Chk1 抑制剂,IC50 为 1.2 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1254 | 有现货 |
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| 10MG | ¥1881 | 有现货 |
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| 25MG | ¥3236 | 有现货 |
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| 50MG | ¥4548 | 有现货 |
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| 100MG | ¥6102 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1378 | 有现货 |
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生物学信息
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产品名称GDC-0575
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述GDC-0575 (ARRY-575, RG-7741) 是一种有效的、选择性的、口服生物可利用的 Chk1 抑制剂,IC50 为 1.2 nM。
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产品描述GDC-0575 (ARRY-575, RG-7741)?is a potent, selective and orally bioavailable Chk1 inhibitor with IC50 of 1.2 nM; enhances the killing of primary AML cells ex vivo by inducing apoptosis combined with AraC, blocks the activation of CHK1 induced by AraC via decrease in the level of Tyr15-phosphorylated CDK2 at 100 nM in AML cells.Blood Cancer Phase 1 Clinical(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. 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. CHK1 inhibitor GDC-0575 in combination with AraC enhances the killing of primary acute myeloid leukemia cells ex vivo by inducing apoptosis.(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.
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体外实验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. 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. CHK1 inhibitor GDC-0575 in combination with AraC enhances the killing of primary acute myeloid leukemia cells ex vivo by inducing apoptosis.
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体内实验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.
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同义词ARRY-575 | RG-7741 | GDC0575
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通路Angiogenesis
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靶点Chk
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受体Chk
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研究领域Cancer
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适应症Blood cancer
化学信息
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CAS Number1196541-47-5
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分子量377.286
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分子式C17H21BrN4O
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 50 mg/mL132.18 mM
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SMILESC1CC(CN(C1)C2=C3C(=CNC3=NC=C2Br)NC(=O)C4CC4)N
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化学全称(R)-N-(4-(3-aminopiperidin-1-yl)-5-bromo-1H-indol-3-yl)cyclopropanecarboxamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Duan W, et al. Front Oncol. 2014 Dec 19;4:368.
2. Di Tullio A, et al. Nat Commun. 2017 Nov 22;8(1):1679.
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