N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide结构式
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常用名 | N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide | 英文名 | N-(2,4,6-trimethylpyridin-3-yl)benzenesulfonamide |
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| CAS号 | 34456-56-9 | 分子量 | 276.35400 | |
| 密度 | 1.252g/cm3 | 沸点 | 411.3ºC at 760mmHg | |
| 分子式 | C14H16N2O2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 202.6ºC |
| 英文名 | 1-[(2R,4S,5R)-4-hydroxy-5-(tritiooxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione |
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| 英文别名 | 更多 |
| 密度 | 1.252g/cm3 |
|---|---|
| 沸点 | 411.3ºC at 760mmHg |
| 分子式 | C14H16N2O2S |
| 分子量 | 276.35400 |
| 闪点 | 202.6ºC |
| 精确质量 | 276.09300 |
| PSA | 67.44000 |
| LogP | 3.96140 |
| InChIKey | BLDIONVFHCVTJL-UHFFFAOYSA-N |
| SMILES | Cc1cc(C)c(NS(=O)(=O)c2ccccc2)c(C)n1 |
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N-(2,4,6-trimet... 34456-56-9 |
| 文献:Adams; Dunbar Journal of the American Chemical Society, 1958 , vol. 80, p. 3649 |
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~%
N-(2,4,6-trimet... 34456-56-9 |
| 文献:Adams; Dunbar Journal of the American Chemical Society, 1958 , vol. 80, p. 3649 |
|
~%
N-(2,4,6-trimet... 34456-56-9 |
| 文献:Adams; Dunbar Journal of the American Chemical Society, 1958 , vol. 80, p. 3649 |
|
~%
N-(2,4,6-trimet... 34456-56-9 |
| 文献:Adams; Dunbar Journal of the American Chemical Society, 1958 , vol. 80, p. 3649 |
|
~%
N-(2,4,6-trimet... 34456-56-9 |
| 文献:Adams; Werbel Journal of the American Chemical Society, 1958 , vol. 80, p. 5799,5802 |
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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...
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External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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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: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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实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
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External Id:HIV1-VIF_MS
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| 3-Benzolsulfonamido-2,4,6-trimethylpyridin |
| 3-Benzosulfamido-2,4,6-trimethylpyridin |