4-(benzenesulfonyl)-1-phenyl-butane-1,3-dione

• 常用名: 4-(benzenesulfonyl)-1-phenyl-butane-1,3-dione
• 英文名: 4-(benzenesulfonyl)-1-phenyl-butane-1,3-dione
• CAS号: 6338-85-8
• 分子量: 302.34500
• 密度: 1.274g/cm3
• 沸点: 510.5ºC at 760 mmHg
• 分子式: C₁₆H₁₄O₄S
• 熔点: N/A
• 闪点: 328.6ºC

名称

• 英文名: 4-(benzenesulfonyl)-1-phenyl-butane-1,3-dione

物理化学性质

• 密度: 1.274g/cm3
• 沸点: 510.5ºC at 760 mmHg
• 分子式: C₁₆H₁₄O₄S
• 分子量: 302.34500
• 闪点: 328.6ºC
• 精确质量: 302.06100
• PSA: 76.66000
• LogP: 3.38320
• InChIKey: GGERDNRGHCSHJP-UHFFFAOYSA-N
• SMILES: O=C(CC(=O)c1ccccc1)CS(=O)(=O)c1ccccc1
• 折射率: 1.58

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

• Niometacinum
• 4-Benzolsulfonyl-1-phenyl-butandion-(1.3)
• Niometacine [INN-French]
• 1-Benzolsulfonyl-4-phenyl-butan-2,4-dion
• Niometacin
• Niometacin [INN]
• <1-Nicotinoyl-2-methyl-5-methoxy-indolyl-(3)>-essigsaeure
• <1-Phenyl-1,3-dioxo-butyl>-phenyl-sulfon
• Niometacina [Spanish]
• (5-methoxy-2-methyl-1-nicotinoyl-indol-3-yl)-acetic acid
• Niometacine [French]
• Niometacina
• Niometacinum [Latin]
• 5-Methoxy-2-methyl-1-nicotinoyl-indol-3-yl-essigsaeure
• 1-phenyl-4-phenylsulfonyl-1,3-butadione
• Niometacine