Pyridine,2-(2,2-diphenylacetamido)- (6CI,7CI)结构式
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常用名 | Pyridine,2-(2,2-diphenylacetamido)- (6CI,7CI) | 英文名 | Pyridine,2-(2,2-diphenylacetamido)- (6CI,7CI) |
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| CAS号 | 94258-23-8 | 分子量 | 288.34300 | |
| 密度 | 1.2g/cm3 | 沸点 | 528.3ºC at 760 mmHg | |
| 分子式 | C19H16N2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 273.3ºC |
| 英文名 | 2,2-diphenyl-N-(2-pyridyl)acetamide |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.2g/cm3 |
|---|---|
| 沸点 | 528.3ºC at 760 mmHg |
| 分子式 | C19H16N2O |
| 分子量 | 288.34300 |
| 闪点 | 273.3ºC |
| 精确质量 | 288.12600 |
| PSA | 41.99000 |
| LogP | 3.92520 |
| InChIKey | KFHRHCHIPAPKLI-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccn1)C(c1ccccc1)c1ccccc1 |
| 折射率 | 1.648 |
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~%
Pyridine,2-(2,2... 94258-23-8 |
| 文献:Ebnoether et al. Helvetica Chimica Acta, 1959 , vol. 42, p. 918,936 |
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~%
Pyridine,2-(2,2... 94258-23-8 |
| 文献:Ebnoether et al. Helvetica Chimica Acta, 1959 , vol. 42, p. 918,936 |
|
~%
Pyridine,2-(2,2... 94258-23-8 |
| 文献:Mndshojan; Afrikjan Izv. Armjansk. Akad.Chem.Abstr., 1957 , vol. 10, p. 143,156 Izv. Armjansk. Akad.Chem.Abstr., 1958 , p. 4641 |
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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...
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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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External Id:CEGtase_01
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