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Quinoxaline,1,2,3,4-tetrahydro-1-(phenylsulfonyl)

更新时间:2025-09-21 09:03:02

Quinoxaline,1,2,3,4-tetrahydro-1-(phenylsulfonyl)结构式
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)
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

 名称

英文名 4-(benzenesulfonyl)-2,3-dihydro-1H-quinoxaline
英文别名 更多

 物理化学性质

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

 靶点实验

查看更多实验

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
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 英文别名

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