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2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide

更新时间:2026-03-30 09:41:26

2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide结构式
2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide结构式
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常用名 2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide 英文名 2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide
CAS号 848595-08-4 分子量 329.4
密度 N/A 沸点 N/A
分子式 C16H12FN3O2S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 2-(3-Fluorophenoxy)-N-[4-(pyridin-2-YL)-1,3-thiazol-2-YL]acetamide

 物理化学性质

分子式 C16H12FN3O2S
分子量 329.4
InChIKey NMSQSTANKRXRFA-UHFFFAOYSA-N
SMILES C1=CC=NC(=C1)C2=CSC(=N2)NC(=O)COC3=CC(=CC=C3)F

 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:Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4296184
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:Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4296185
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:Compound was evaluated for the inhibition of human FECH at 10uM
来源:ChEMBL
靶标:Ferrochelatase, mitochondrial
External Id:CHEMBL3987222
实验名称:Compound was evaluated for the inhibition of human HMBS at 100uM
来源:ChEMBL
靶标:Porphobilinogen deaminase
External Id:CHEMBL3987223
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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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