KRAS inhibitor-9
CAS No. 300809-71-6
KRAS inhibitor-9 ( DUN09716 )
产品货号. M22747 CAS No. 300809-71-6
KRAS抑制剂-9是一种有效的KRAS抑制剂,Kd为92 μM,可阻断GTP-KRAS的形成和KRAS下游的激活。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥654 | 有现货 |
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| 5MG | ¥1121 | 有现货 |
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| 10MG | ¥1881 | 有现货 |
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| 25MG | ¥3339 | 有现货 |
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| 50MG | ¥4613 | 有现货 |
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| 100MG | ¥6165 | 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 | ¥1207 | 有现货 |
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生物学信息
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产品名称KRAS inhibitor-9
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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KRAS抑制剂-9是一种有效的KRAS抑制剂,Kd为92 μM,可阻断GTP-KRAS的形成和KRAS下游的激活。
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产品描述KRAS inhibitor-9 is a potent KRAS inhibitor with Kd of 92 μM that blocks the formation of GTP-KRAS and downstream activation of KRAS.??KRAS inhibitor-9 causes G2/M cell cycle arrest and induces apoptosis. KRAS inhibitor-9 selectively inhibits the proliferation of NSCLC cells with KRAS mutation but not normal lung cells
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体外实验KRAS inhibitor-9 bound to KRASG12D, KRAS G12C and KRAS Q61H protein with a moderate binding affinity of -5.38, -5.41, and -3.97 kcal/mol, respectively. KRAS inhibitor-9 (0-100 μM) shows strong inhibition selectivity in NSCLC cells with IC50s ranging from 39.56 to 66.02 μM for H2122, H358 and H460 cells (at 72 hours).KRAS inhibitor-9 (0-100 μM; 24 hours) blocks GTP-KRAS formation in H2122, H358 and H460 cells.KRAS inhibitor-9 (25-100 μM; 48 hours) inhibits the activation of KRAS downstream signaling pathway.KRAS inhibitor-9 (0-100 μM; 24-72 hours) induces cell cycle arrest and apoptosis in NSCLC. Cell Viability Assay Cell Line:H2122 (KRAS G12C), H358 (KRAS G12C) and H460 (KRAS Q61H) cell lines Concentration:0, 25, 50, 100 μM Incubation Time:24, 48, and 72 hoursResult:Inhibited three NSCLC cell lines in a dose- and time-dependent manner, but not in normal lung fibroblast cell line CCD-19Lu.Western Blot Analysis Cell Line:H2122, H358 and H460 cells Concentration:0, 25, 50, 100 μM Incubation Time:48 hours Result:Reduces the levels of phosphorylation of CRAF and AKT in a dose-dependent manner in H2122, H358 and H460 cells.Apoptosis Analysis Cell Line:H2122, H358, H460 cellsConcentration:0, 25, 50, 100 μM Incubation Time:24-72 hours Result:Significantly decreased in G0/G1 phase while remarkably increased in G2/M phase after 24 hours and induced a significantly increased apoptosis for 48h in NSCLC cell lines.
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体内实验——
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同义词DUN09716
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通路MAPK/ERK Signaling
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靶点Ras
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受体KRAS
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研究领域——
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适应症——
化学信息
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CAS Number300809-71-6
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分子量292.8
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分子式C13H9ClN2S2?
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纯度>98% (HPLC)
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溶解度DMSO:230 mg/mL?(785.49 mM;?Need ultrasonic)
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SMILESNc1ccc(Sc2nc3ccccc3s2)c(Cl)c1
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化学全称——
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.Xie C, et al. Identification of a New Potent Inhibitor Targeting KRAS in Non-small Cell Lung Cancer Cells. Front Pharmacol. 2017;8:823. Published 2017 Nov 14.
产品手册
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