4-((3,4-dihydroisoquinolin-2(1H)-yl)sulfonyl)-N-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)benzamide结构式
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常用名 | 4-((3,4-dihydroisoquinolin-2(1H)-yl)sulfonyl)-N-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)benzamide | 英文名 | 4-((3,4-dihydroisoquinolin-2(1H)-yl)sulfonyl)-N-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)benzamide |
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| CAS号 | 533869-60-2 | 分子量 | 478.5 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C24H19FN4O4S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 4-((3,4-dihydroisoquinolin-2(1H)-yl)sulfonyl)-N-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)benzamide |
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| 分子式 | C24H19FN4O4S |
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| 分子量 | 478.5 |
| InChIKey | QHVHZTSQOKOPCV-UHFFFAOYSA-N |
| SMILES | C1CN(CC2=CC=CC=C21)S(=O)(=O)C3=CC=C(C=C3)C(=O)NC4=NN=C(O4)C5=CC=C(C=C5)F |
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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:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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实验名称:Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
来源:24983
靶标:Huntingtin
External Id:KUHTS-Muma KU-CaM-Htt INH-01
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