
PBRM1-BD2-IN-8
CAS No. 2819989-75-6
PBRM1-BD2-IN-8 ( —— )
产品货号. M35350 CAS No. 2819989-75-6
PBRM1-BD2-IN-8 (compound 34) 是一种强效的 PBRM1 Bromodomain 抑制剂 (PBRM1-BD2 Kd=4.4 μM, PBRM1-BD2 IC50=0.16 μM; PBRM1-BD5 Kd=25 μM),其具有抗癌活性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥1266 | 有现货 |
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5MG | ¥2091 | 有现货 |
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10MG | ¥3036 | 有现货 |
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25MG | ¥4575 | 有现货 |
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50MG | ¥6053 | 有现货 |
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100MG | ¥8109 | 有现货 |
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500MG | ¥16295 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称PBRM1-BD2-IN-8
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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PBRM1-BD2-IN-8 (compound 34) 是一种强效的 PBRM1 Bromodomain 抑制剂 (PBRM1-BD2 Kd=4.4 μM, PBRM1-BD2 IC50=0.16 μM; PBRM1-BD5 Kd=25 μM),其具有抗癌活性。
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产品描述PBRM1-BD2-IN-8 (compound 34) is a potent PBRM1 Bromodomain inhibitor (PBRM1-BD2 Kd=4.4 μM, PBRM1-BD2 IC50=0.16 μM; PBRM1-BD5 Kd=25 μM). PBRM1-BD2-IN-8 shows anti-cancer activity.
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体外实验PBRM1-BD2-IN-8 (0-100 μM; 48 h) inhibits the growth of PBRM1-dependent prostate cancer cells.Cell Viability AssayCell Line:LNCaP cells Concentration:0-100 μM Incubation Time:48 hours Result:Inhibited the growth of LNCaP cells with IC50 value of about 9 μM.
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体内实验——
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同义词——
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通路Chromatin/Epigenetic
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靶点Epigenetic Reader Domain
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受体Epigenetic Reader Domain
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研究领域——
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适应症——
化学信息
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CAS Number2819989-75-6
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分子量317.18
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分子式C15H13BrN2O
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (315.28 mM; 超声助溶 )
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SMILESO=C1C=2C(NC(N1)C3=CC(C)=CC=C3)=CC=CC2Br
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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. Shishodia S, et al. Selective and Cell-Active PBRM1 Bromodomain Inhibitors Discovered through NMR Fragment Screening. J Med Chem. 2022 Oct 13.?
产品手册




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