Benzenesulfonamide,N-[1,1'-biphenyl]-4-yl结构式
|
常用名 | Benzenesulfonamide,N-[1,1'-biphenyl]-4-yl | 英文名 | Benzenesulfonamide,N-[1,1'-biphenyl]-4-yl |
|---|---|---|---|---|
| CAS号 | 13607-48-2 | 分子量 | 309.38200 | |
| 密度 | 1.268g/cm3 | 沸点 | 484.7ºC at 760mmHg | |
| 分子式 | C18H15NO2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 247ºC |
| 英文名 | N-(4-phenylphenyl)benzenesulfonamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.268g/cm3 |
|---|---|
| 沸点 | 484.7ºC at 760mmHg |
| 分子式 | C18H15NO2S |
| 分子量 | 309.38200 |
| 闪点 | 247ºC |
| 精确质量 | 309.08200 |
| PSA | 54.55000 |
| LogP | 5.30820 |
| InChIKey | JMNQYDKGYHLAMY-UHFFFAOYSA-N |
| SMILES | O=S(=O)(Nc1ccc(-c2ccccc2)cc1)c1ccccc1 |
| 蒸汽压 | 1.5E-09mmHg at 25°C |
| 折射率 | 1.647 |
| 储存条件 | 库房通风低温干燥 |
|
~%
Benzenesulfonam... 13607-48-2 |
| 文献:Raiford; Hazlet Journal of the American Chemical Society, 1935 , vol. 57, p. 2172 |
| 上游产品 2 | |
|---|---|
| 下游产品 0 | |
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
| Benzenesulfonanilide,4'-phenyl |
| N-4-Biphenylbenzenesulfonamide |
| 4-Benzolsulfonylamino-biphenyl |
| WLN: WSR&MR DR |
| Benzenesulfonamide,N-4-biphenylyl |
| N-biphenyl-4-yl-benzenesulfonamide |
| N-4-Biphenylylbenzenesulfonamide |
| N-Biphenyl-4-yl-benzolsulfonamid |