N,2-diphenylethanethioamide

• 常用名: N,2-diphenylethanethioamide
• 英文名: N,2-diphenylethanethioamide
• CAS号: 6636-01-7
• 分子量: 227.32500
• 密度: 1.189g/cm3
• 沸点: 357.7ºC at 760 mmHg
• 分子式: C₁₄H₁₃NS
• 熔点: N/A
• 闪点: 170.1ºC

N,2-diphenylethanethioamide名称

• 英文名: N,2-diphenylethanethioamide

N,2-diphenylethanethioamide物理化学性质

• 密度: 1.189g/cm3
• 沸点: 357.7ºC at 760 mmHg
• 分子式: C₁₄H₁₃NS
• 分子量: 227.32500
• 闪点: 170.1ºC
• 精确质量: 227.07700
• PSA: 44.12000
• LogP: 3.74160
• InChIKey: DBWIGILQUWIQTL-UHFFFAOYSA-N
• SMILES: S=C(Cc1ccccc1)Nc1ccccc1
• 折射率: 1.68

N,2-diphenylethanethioamide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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N,2-diphenylethanethioamide英文别名

• phenyl-thioacetic acid anilide
• Phenyl-thioessigsaeure-anilid
• 1-phenylthioacetanilide
• Phenylthioacetanilid
• N-Phenyl-<phenyl-thioacetamid>
• HMS3089J11