2-Thiazolamine,N-(2,6-dichlorophenyl)-4,5-dihydro

• 常用名: 2-Thiazolamine,N-(2,6-dichlorophenyl)-4,5-dihydro
• 英文名: 2-Thiazolamine,N-(2,6-dichlorophenyl)-4,5-dihydro
• CAS号: 29263-30-7
• 分子量: 247.14400
• 密度: 1.51g/cm3
• 沸点: 347.4ºC at 760mmHg
• 分子式: C₉H₈Cl₂N₂S
• 熔点: N/A
• 闪点: 163.9ºC

名称

• 英文名: N-(2,6-dichlorophenyl)-4,5-dihydro-1,3-thiazol-2-amine

物理化学性质

• 密度: 1.51g/cm3
• 沸点: 347.4ºC at 760mmHg
• 分子式: C₉H₈Cl₂N₂S
• 分子量: 247.14400
• 闪点: 163.9ºC
• 精确质量: 245.97900
• PSA: 49.69000
• LogP: 3.01670
• InChIKey: LVEOATNALAMZRX-UHFFFAOYSA-N
• SMILES: Clc1cccc(Cl)c1NC1=NCCS1
• 蒸汽压: 5.41E-05mmHg at 25°C
• 折射率: 1.686

靶点实验

查看更多实验

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：A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School External Id：HMS979

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：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

实验名称：EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Rea... 来源：Broad Institute 靶标：histone-lysine N-methyltransferase EZH2 isoform a [Homo sapiens] External Id：2125-01_Inhibitor_SinglePoint_HTS_Activity

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英文别名

• (2,6-dichloro-phenyl)-(4,5-dihydro-thiazol-2-yl)-amine
• 2-(o,o'-Dichlorphenylamino)-2-thiazolin
• HMS1531I13