Quinoxaline,1,2,3,4-tetrahydro-1-(phenylsulfonyl)结构式
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常用名 | Quinoxaline,1,2,3,4-tetrahydro-1-(phenylsulfonyl) | 英文名 | Quinoxaline,1,2,3,4-tetrahydro-1-(phenylsulfonyl) |
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| CAS号 | 6344-73-6 | 分子量 | 274.33800 | |
| 密度 | 1.302g/cm3 | 沸点 | 457.3ºC at 760 mmHg | |
| 分子式 | C14H14N2O2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 230.4ºC |
| 英文名 | 4-(benzenesulfonyl)-2,3-dihydro-1H-quinoxaline |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.302g/cm3 |
|---|---|
| 沸点 | 457.3ºC at 760 mmHg |
| 分子式 | C14H14N2O2S |
| 分子量 | 274.33800 |
| 闪点 | 230.4ºC |
| 精确质量 | 274.07800 |
| PSA | 57.79000 |
| LogP | 3.59120 |
| InChIKey | DTFRZJVIPOKBRW-UHFFFAOYSA-N |
| SMILES | O=S(=O)(c1ccccc1)N1CCNc2ccccc21 |
| 折射率 | 1.63 |
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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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| hms3089g09 |