N-((1-phenyl-1H-tetrazol-5-yl)methyl)-2-naphthamide结构式
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常用名 | N-((1-phenyl-1H-tetrazol-5-yl)methyl)-2-naphthamide | 英文名 | N-((1-phenyl-1H-tetrazol-5-yl)methyl)-2-naphthamide |
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| CAS号 | 897615-06-4 | 分子量 | 329.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H15N5O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
本表展示该化学物质的中文名称、英文系统名、各类中文与英文别名信息。
| 英文名 | N-((1-phenyl-1H-tetrazol-5-yl)methyl)-2-naphthamide |
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本表包含该物质理化参数,如熔点、沸点、密度、溶解度、旋光性等理化指标,无数据项标记为N/A。
| 分子式 | C19H15N5O |
|---|---|
| 分子量 | 329.4 |
| InChIKey | QAJIHQNITBQGHP-UHFFFAOYSA-N |
| SMILES | O=C(NCc1nnnn1-c1ccccc1)c1ccc2ccccc2c1 |
本表记录该化合物靶点、体外体内实验、生物测定实验相关实验数据。
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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
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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
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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
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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
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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
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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
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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
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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
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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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实验名称:Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition
来源:Southern Research Specialized Biocontainment Screening Center
靶标:Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocysteine
External Id:CEGtase_01
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本部分为该化合物相关常见问答,包含基础参数、性状、储存条件等高频咨询问题与对应答案。
| Q: 897615-06-4的英文名称是什么? |
| A: 897615-06-4英文名称为N-((1-phenyl-1H-tetrazol-5-yl)methyl)-2-naphthamide。 |
| Q: 897615-06-4的SMILES表达式是什么? |
| A: 897615-06-4SMILES表达式为O=C(NCc1nnnn1-c1ccccc1)c1ccc2ccccc2c1。 |
| Q: 897615-06-4的制备方法是什么? |
| A: 897615-06-4制备方法:O=C(NCc1nnnn1-c1ccccc1)c1ccc2ccccc2c1。 |
| Q: 897615-06-4的分子式是什么? |
| A: 897615-06-4分子式为C19H15N5O。 |
| Q: 897615-06-4的中文名称是什么? |
| A: 897615-06-4的中文名称为897615-06-4。 |
| Q: 897615-06-4的InChIKey是什么? |
| A: 897615-06-4InChIKey为QAJIHQNITBQGHP-UHFFFAOYSA-N。 |
| Q: 897615-06-4的CAS号是多少? |
| A: 897615-06-4CAS号为897615-06-4。 |
| Q: 897615-06-4的分子量是多少? |
| A: 897615-06-4分子量为329.4。 |