N-benzyl-N-hydroxy-benzenecarboximidamide结构式
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常用名 | N-benzyl-N-hydroxy-benzenecarboximidamide | 英文名 | N-benzyl-N-hydroxy-benzenecarboximidamide |
|---|---|---|---|---|
| CAS号 | 3488-55-9 | 分子量 | 226.27400 | |
| 密度 | 1.08g/cm3 | 沸点 | 384.8ºC at 760 mmHg | |
| 分子式 | C14H14N2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 186.5ºC |
| 英文名 | N-benzyl-N'-hydroxybenzimidamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.08g/cm3 |
|---|---|
| 沸点 | 384.8ºC at 760 mmHg |
| 分子式 | C14H14N2O |
| 分子量 | 226.27400 |
| 闪点 | 186.5ºC |
| 精确质量 | 226.11100 |
| PSA | 44.62000 |
| LogP | 3.00310 |
| InChIKey | JPXBMIZUWYDMSO-UHFFFAOYSA-N |
| SMILES | ONC(=NCc1ccccc1)c1ccccc1 |
| 折射率 | 1.578 |
|
~78%
N-benzyl-N-hydr... 3488-55-9 |
| 文献:Chen, Hui; Chiba, Shunsuke Organic and Biomolecular Chemistry, 2014 , vol. 12, # 1 p. 42 - 46 |
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~%
N-benzyl-N-hydr... 3488-55-9 |
| 文献:Burgess,E.M.; Lavanish,J.M. Tetrahedron Letters, 1964 , # 20 p. 1221 - 1226 |
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~%
N-benzyl-N-hydr... 3488-55-9 |
| 文献:Takacs,K.; Harsanyi,K. Chemische Berichte, 1970 , vol. 103, p. 2330 - 2335 |
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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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: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: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: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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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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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:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
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| N-benzyl-N'-hydroxy-benzamidine |
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