N-Methyl-2-{[5-phenyl-2-(pyridin-2-YL)thieno[2,3-D]pyrimidin-4-YL]amino}acetamide结构式
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常用名 | N-Methyl-2-{[5-phenyl-2-(pyridin-2-YL)thieno[2,3-D]pyrimidin-4-YL]amino}acetamide | 英文名 | N-Methyl-2-{[5-phenyl-2-(pyridin-2-YL)thieno[2,3-D]pyrimidin-4-YL]amino}acetamide |
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| CAS号 | 920825-79-2 | 分子量 | 375.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C20H17N5OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | N-Methyl-2-{[5-phenyl-2-(pyridin-2-YL)thieno[2,3-D]pyrimidin-4-YL]amino}acetamide |
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| 分子式 | C20H17N5OS |
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| 分子量 | 375.4 |
| InChIKey | RBKVRSJNDSUKEM-UHFFFAOYSA-N |
| SMILES | CNC(=O)CNc1nc(-c2ccccn2)nc2scc(-c3ccccc3)c12 |
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实验名称:Antimalarial activity: Asexual Blood Stage Plasmodium falciparum 3D7 IC50 (uM)
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL3832778
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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
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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
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实验名称:Luciferase/luciferin-expressing antifolate-resistant parasites were used to infect a ...
来源:ChEMBL
靶标:HepG2-CD81
External Id:CHEMBL4483864
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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
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实验名称:Luciferase/luciferin-expressing antifolate-resistant parasites were used to infect a ...
来源:ChEMBL
靶标:Plasmodium berghei
External Id:CHEMBL4483863
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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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
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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
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