1-phenyl-4-pyridin-2-yl-butan-1-one结构式
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常用名 | 1-phenyl-4-pyridin-2-yl-butan-1-one | 英文名 | 1-phenyl-4-pyridin-2-yl-butan-1-one |
|---|---|---|---|---|
| CAS号 | 7153-77-7 | 分子量 | 225.28600 | |
| 密度 | 1.083g/cm3 | 沸点 | 374.1ºC at 760 mmHg | |
| 分子式 | C15H15NO | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 187.5ºC |
| 英文名 | 1-phenyl-4-pyridin-2-ylbutan-1-one |
|---|
| 密度 | 1.083g/cm3 |
|---|---|
| 沸点 | 374.1ºC at 760 mmHg |
| 分子式 | C15H15NO |
| 分子量 | 225.28600 |
| 闪点 | 187.5ºC |
| 精确质量 | 225.11500 |
| PSA | 29.96000 |
| LogP | 3.28720 |
| InChIKey | CRUVDMPFOYFNCE-UHFFFAOYSA-N |
| SMILES | O=C(CCCc1ccccn1)c1ccccc1 |
| 折射率 | 1.569 |
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~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Levine; Wilt Journal of the American Chemical Society, 1952 , vol. 74, p. 342 |
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~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Levine; Wilt Journal of the American Chemical Society, 1952 , vol. 74, p. 342 View citing articles Show Details Boekelheide; Agnello Journal of the American Chemical Society, 1950 , vol. 72, p. 5005,5006 |
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~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Boekelheide; Agnello Journal of the American Chemical Society, 1950 , vol. 72, p. 5005,5006 |
|
~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Boekelheide; Agnello Journal of the American Chemical Society, 1950 , vol. 72, p. 5005,5006 |
|
~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Shono et al. Kogyo Kagaku Zasshi, 1954 , vol. 57, p. 902 Chem.Abstr., 1956 , p. 999 |
|
~%
1-phenyl-4-pyri... 7153-77-7 |
| 文献:Shono et al. Kogyo Kagaku Zasshi, 1954 , vol. 57, p. 902 Chem.Abstr., 1956 , p. 999 |
| 1-phenyl-4-pyridin-2-yl-butan-1-one上游产品 6 | |
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| 1-phenyl-4-pyridin-2-yl-butan-1-one下游产品 1 | |
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
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实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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实验名称:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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