4-Thiazolecarboxamide,2-[2-(benzoylamino)ethyl]

• 常用名: 4-Thiazolecarboxamide,2-[2-(benzoylamino)ethyl]
• 英文名: 4-Thiazolecarboxamide,2-[2-(benzoylamino)ethyl]
• CAS号: 30761-32-1
• 分子量: 275.32600
• 密度: 1.321g/cm3
• 沸点: 604.3ºC at 760mmHg
• 分子式: C₁₃H₁₃N₃O₂S
• 熔点: N/A
• 闪点: 319.3ºC

名称

• 英文名: 2-(2-benzamidoethyl)-1,3-thiazole-4-carboxamide

物理化学性质

• 密度: 1.321g/cm3
• 沸点: 604.3ºC at 760mmHg
• 分子式: C₁₃H₁₃N₃O₂S
• 分子量: 275.32600
• 闪点: 319.3ºC
• 精确质量: 275.07300
• PSA: 113.32000
• LogP: 2.30570
• InChIKey: MGKRHDNQZQRXOB-UHFFFAOYSA-N
• SMILES: NC(=O)c1csc(CCNC(=O)c2ccccc2)n1
• 折射率: 1.632

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：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：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

实验名称：Fluorescence polarization-based biochemical high throughput primary assay to identify... 来源：The Scripps Research Institute Molecular Screening Center 靶标：abhydrolase domain-containing protein 4 isoform 1 [Mus musculus] External Id：ABHD4_INH_FP_1536_1X%INH PRUN

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英文别名

• 2-[2-(benzoylamino)ethyl]-1,3-thiazole-4-carboxamide
• 2-(2-Benzamidoaethyl)-thiazol-4-carbonamid
• 2-(2-benzoylamino-ethyl)-thiazole-4-carboxylic acid amide