N-(2-Aminophenyl)-4-methoxybenzamide结构式
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常用名 | N-(2-Aminophenyl)-4-methoxybenzamide | 英文名 | N-(2-Aminophenyl)-4-methoxybenzamide |
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| CAS号 | 263841-87-8 | 分子量 | 242.27 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C14H14N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | N-(2-Aminophenyl)-4-methoxybenzamide |
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| 分子式 | C14H14N2O2 |
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| 分子量 | 242.27 |
| InChIKey | BDYVCYUXCNZYRW-UHFFFAOYSA-N |
| SMILES | COC1=CC=C(C=C1)C(=O)NC2=CC=CC=C2N |
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实验名称:qHTS screening for TAG (triacylglycerol) accumulators in algae
来源:11812
靶标:N/A
External Id:FATTTLab-Algae-Lipid
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实验名称:HDAC Enzyme Activity Assay from Article 10.1021/jm701079h: "Novel aminophenyl benzami...
来源:BindingDB
靶标:N/A
External Id:BindingDB_2322_1
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实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
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实验名称:Inhibition of human recombinant HDAC1 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 1
External Id:CHEMBL900129
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实验名称:Inhibition of human recombinant HDAC2 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 2
External Id:CHEMBL900130
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:Inhibition of human recombinant HDAC6 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL900135
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实验名称:Inhibition of human recombinant HDAC7 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 7
External Id:CHEMBL900136
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实验名称:Inhibition of human recombinant HDAC3 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 3
External Id:CHEMBL900131
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实验名称:Inhibition of human recombinant HDAC8 at 20 uM
来源:ChEMBL
靶标:Histone deacetylase 8
External Id:CHEMBL900132
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