Benzenesulfonamide,2,4,6-trimethyl-N-phenyl

• 常用名: Benzenesulfonamide,2,4,6-trimethyl-N-phenyl
• 英文名: Benzenesulfonamide,2,4,6-trimethyl-N-phenyl
• CAS号: 25116-87-4
• 分子量: 275.36600
• 密度: 1.211g/cm3
• 沸点: 421ºC at 760mmHg
• 分子式: C₁₅H₁₇NO₂S
• 熔点: N/A
• 闪点: 208.4ºC

名称

• 英文名: 2-Mesitylenesulfonanilide

物理化学性质

• 密度: 1.211g/cm3
• 沸点: 421ºC at 760mmHg
• 分子式: C₁₅H₁₇NO₂S
• 分子量: 275.36600
• 闪点: 208.4ºC
• 精确质量: 275.09800
• PSA: 54.55000
• LogP: 4.56640
• InChIKey: ARIRERZAGIDHFR-UHFFFAOYSA-N
• SMILES: Cc1cc(C)c(S(=O)(=O)Nc2ccccc2)c(C)c1
• 蒸汽压: 2.7E-07mmHg at 25°C
• 折射率: 1.6

靶点实验

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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

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：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

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英文别名

• N-phenylmesitylsulfonamide
• N-Phenylmercaptocarbonyl-glycin-aethylester
• 2,4,6-trimethyl-benzenesulfonic acid anilide
• N-<Phenyl-thio-carbonyl>-glycin-ethylester
• N-phenylsulfanylcarbonyl-glycine ethyl ester
• 2,4,6-Trimethyl-phenylsulfonsaeure-anilid
• Phenylmercaptocarbonylamino-essigsaeure-aethylester
• N-phenyl mesitylenesulfonamide
• 2,4,6-Trimethyl-benzolsulfonsaeure-anilid