3-(1H-benzo[d]imidazol-2-yl)-6-ethyl-7-hydroxy-8-((4-methylpiperidin-1-yl)methyl)-4H-chromen-4-one结构式
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常用名 | 3-(1H-benzo[d]imidazol-2-yl)-6-ethyl-7-hydroxy-8-((4-methylpiperidin-1-yl)methyl)-4H-chromen-4-one | 英文名 | 3-(1H-benzo[d]imidazol-2-yl)-6-ethyl-7-hydroxy-8-((4-methylpiperidin-1-yl)methyl)-4H-chromen-4-one |
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| CAS号 | 637747-27-4 | 分子量 | 417.5 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C25H27N3O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 3-(1H-benzo[d]imidazol-2-yl)-6-ethyl-7-hydroxy-8-((4-methylpiperidin-1-yl)methyl)-4H-chromen-4-one |
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| 分子式 | C25H27N3O3 |
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| 分子量 | 417.5 |
| InChIKey | KINIMPMVNCSFNS-UHFFFAOYSA-N |
| SMILES | CCC1=CC2=C(C(=C1O)CN3CCC(CC3)C)OC=C(C2=O)C4=NC5=CC=CC=C5N4 |
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实验名称:HTS to identify inhibitors of TNF-alpha Induced Cell Death in Jurkat FADD-/- Cells.
来源:University of Pittsburgh Molecular Library Screening Center
靶标:N/A
External Id:MH081226: Primary HTS for Inhibitors of a Novel Necrotic Cell Death Pathway # Jurkat FADD-/- Model.
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实验名称:384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC
来源:University of Pittsburgh Molecular Library Screening Center
靶标:N/A
External Id:MH083223 Targeting HIV-1 Nef with Small Molecules
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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