PBRM1-BD2-IN-6结构式
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常用名 | PBRM1-BD2-IN-6 | 英文名 | PBRM1-BD2-IN-6 |
|---|---|---|---|---|
| CAS号 | 2819989-67-6 | 分子量 | 286.76 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H15ClN2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
PBRM1-BD2-IN-6用途PBRM1-BD2-IN-6是一种有效的PBRM1溴域抑制剂,IC50值为0.22µM。PBRM1-BD2-IN-6显示出抗增殖活性。PBRM1-BD2-IN-6具有研究PBRM1依赖性癌症的潜力[1]。 |
| 英文名 | PBRM1-BD2-IN-6 |
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| 描述 | PBRM1-BD2-IN-6是一种有效的PBRM1溴域抑制剂,IC50值为0.22µM。PBRM1-BD2-IN-6显示出抗增殖活性。PBRM1-BD2-IN-6具有研究PBRM1依赖性癌症的潜力[1]。 |
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| 相关类别 | |
| 靶点实验 |
IC50: 0.22 nM (PBRM1-BD2)[1] |
| 体外研究 | PBRM1-BD2-IN-6(化合物25)(0.1、1、10μM;5天)显示出抗增殖活性,LNCaP、PC3和HEK293T细胞的IC50值分别为0.66、0.77和0.32µM[1]。细胞增殖测定[1]细胞系:LNCaP、PC3、HEK293T细胞浓度:0.1、1、10μM培养时间:5天结果:抑制细胞生长,LNCaP,PC3,HEK293T细胞的IC50值分别为0.66、0.77、0.32μM。 |
| 分子式 | C16H15ClN2O |
|---|---|
| 分子量 | 286.76 |
| InChIKey | VQRNXAWCBAQDHZ-UHFFFAOYSA-N |
| SMILES | Cc1cccc(C2NC(=O)c3c(Cl)cccc3N2)c1C |
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实验名称:Cytotoxicity against HEK293T cells assessed as inhibition of cell growth at 1 to 10 u...
来源:ChEMBL
靶标:HEK-293T
External Id:CHEMBL5112666
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实验名称:Inhibition of biotinylated histone H3K14 (1 to 20 residues) peptide binding to His6-t...
来源:ChEMBL
靶标:Protein polybromo-1
External Id:CHEMBL5112650
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实验名称:Cytotoxicity against human RWPE-1 cells assessed as inhibition of cell growth at 1 to...
来源:ChEMBL
靶标:RWPE-1
External Id:CHEMBL5112668
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实验名称:Binding affinity to 15N-labeled recombinant human PBRM1 BD2 transfected in Escherichi...
来源:ChEMBL
靶标:Protein polybromo-1
External Id:CHEMBL5112649
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实验名称:Cytotoxicity against human PC-3 cells assessed as inhibition of cell growth at 1 to 1...
来源:ChEMBL
靶标:PC-3
External Id:CHEMBL5112670
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实验名称:AlphaScreen assay from US Patent US20240190828: "Small Molecule Inhibitors of PBRM1-B...
来源:BindingDB
靶标:N/A
External Id:BindingDB_12220_1
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