N-(2,2-diphenylcyclopropyl)benzamide结构式
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常用名 | N-(2,2-diphenylcyclopropyl)benzamide | 英文名 | N-(2,2-diphenylcyclopropyl)benzamide |
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| CAS号 | 4941-62-2 | 分子量 | 313.39200 | |
| 密度 | 1.19g/cm3 | 沸点 | 522.2ºC at 760 mmHg | |
| 分子式 | C22H19NO | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 317ºC |
| 英文名 | N-(2,2-diphenylcyclopropyl)benzamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.19g/cm3 |
|---|---|
| 沸点 | 522.2ºC at 760 mmHg |
| 分子式 | C22H19NO |
| 分子量 | 313.39200 |
| 闪点 | 317ºC |
| 精确质量 | 313.14700 |
| PSA | 29.10000 |
| LogP | 4.56590 |
| InChIKey | ZMMBJYSRTXCIDR-UHFFFAOYSA-N |
| SMILES | O=C(NC1CC1(c1ccccc1)c1ccccc1)c1ccccc1 |
| 折射率 | 1.656 |
| N-(2,2-diphenylcyclopropyl)benzamide上游产品 2 | |
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| N-(2,2-diphenylcyclopropyl)benzamide下游产品 0 | |
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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: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: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
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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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| N-<2,2-Diphenyl-cyclopropyl>-benzamid |
| N-Benzoyl-1,1-diphenyl-2-aminocyclopropan |