2-benzyl-3-phenyl-prop-2-enoic acid结构式
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常用名 | 2-benzyl-3-phenyl-prop-2-enoic acid | 英文名 | 2-benzyl-3-phenyl-prop-2-enoic acid |
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| CAS号 | 4361-83-5 | 分子量 | 238.28100 | |
| 密度 | 1.179g/cm3 | 沸点 | 406ºC at 760 mmHg | |
| 分子式 | C16H14O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 302ºC |
| 英文名 | 2-benzyl-3-phenylprop-2-enoic acid |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.179g/cm3 |
|---|---|
| 沸点 | 406ºC at 760 mmHg |
| 分子式 | C16H14O2 |
| 分子量 | 238.28100 |
| 闪点 | 302ºC |
| 精确质量 | 238.09900 |
| PSA | 37.30000 |
| LogP | 3.39730 |
| InChIKey | KNEFRHCUYCDKRK-UHFFFAOYSA-N |
| SMILES | O=C(O)C(=Cc1ccccc1)Cc1ccccc1 |
| 折射率 | 1.638 |
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2-benzyl-3-phen... 4361-83-5 |
| 文献:Oglialoro Gazzetta Chimica Italiana, 1890 , vol. 20, p. 163 |
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2-benzyl-3-phen... 4361-83-5 |
| 文献:Moriconi,E.J.; Kelly,J.F. Journal of Organic Chemistry, 1968 , vol. 33, # 8 p. 3036 - 3046 |
| 2-benzyl-3-phenyl-prop-2-enoic acid上游产品 2 | |
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| 2-benzyl-3-phenyl-prop-2-enoic acid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
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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...
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靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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