2-Pyridineethanamine,N-(2-thienylmethyl)

• 常用名: 2-Pyridineethanamine,N-(2-thienylmethyl)
• 英文名: 2-Pyridineethanamine,N-(2-thienylmethyl)
• CAS号: 6973-67-7
• 分子量: 218.31800
• 密度: 1.143g/cm3
• 沸点: 340.3ºC at 760 mmHg
• 分子式: C₁₂H₁₄N₂S
• 熔点: N/A
• 闪点: 159.6ºC

2-Pyridineethanamine,N-(2-thienylmethyl)名称

• 英文名: 2-pyridin-2-yl-N-(thiophen-2-ylmethyl)ethanamine

2-Pyridineethanamine,N-(2-thienylmethyl)物理化学性质

• 密度: 1.143g/cm3
• 沸点: 340.3ºC at 760 mmHg
• 分子式: C₁₂H₁₄N₂S
• 分子量: 218.31800
• 闪点: 159.6ºC
• 精确质量: 218.08800
• PSA: 53.16000
• LogP: 2.86630
• InChIKey: APEACHBNZNBVMA-UHFFFAOYSA-N
• SMILES: c1ccc(CCNCc2cccs2)nc1
• 折射率: 1.596

2-Pyridineethanamine,N-(2-thienylmethyl)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：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

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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2-Pyridineethanamine,N-(2-thienylmethyl)英文别名

• (2-[2]Pyridyl-aethyl)-[2]thienylmethyl-amin
• 2-(pyridin-2-yl)-n-(thiophen-2-ylmethyl)ethanamine
• (2-[2]pyridyl-ethyl)-[2]thienylmethyl-amine