(4-amino-2-benzylsulfanyl-1,3-thiazol-5-yl)-(1-piperidyl)methanone

• 常用名: (4-amino-2-benzylsulfanyl-1,3-thiazol-5-yl)-(1-piperidyl)methanone
• 英文名: (4-amino-2-benzylsulfanyl-1,3-thiazol-5-yl)-(1-piperidyl)methanone
• CAS号: 63238-13-1
• 分子量: 333.47200
• 密度: 1.33g/cm3
• 沸点: 568.8ºC at 760 mmHg
• 分子式: C₁₆H₁₉N₃OS₂
• 熔点: N/A
• 闪点: 297.8ºC

名称

• 英文名: (4-amino-2-benzylsulfanyl-1,3-thiazol-5-yl)-piperidin-1-ylmethanone

物理化学性质

• 密度: 1.33g/cm3
• 沸点: 568.8ºC at 760 mmHg
• 分子式: C₁₆H₁₉N₃OS₂
• 分子量: 333.47200
• 闪点: 297.8ºC
• 精确质量: 333.09700
• PSA: 112.76000
• LogP: 4.16280
• InChIKey: ZJFWHKJKIZTTEH-UHFFFAOYSA-N
• SMILES: Nc1nc(SCc2ccccc2)sc1C(=O)N1CCCCC1
• 折射率: 1.672

靶点实验

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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：Confirm compound inhibition to esBAF complex through repress target gene Fgf4 in qPCR... 来源：Broad Institute 靶标：N/A External Id：2141-03_Inhibitor_SinglePoint_CherryPick_Activity

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：Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ... 来源：ChEMBL 靶标：Klebsiella pneumoniae External Id：CHEMBL4296186

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：Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay 来源：24386 靶标：N/A External Id：Sarm1 TIR NADase inhibitors

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英文别名

• 4-Amino-2-benzylthio-5-thiazol-(N,N-pentamethylencarboxamid)
• 1-(4-amino-2-benzylsulfanyl-thiazole-5-carbonyl)-piperidine