6-benzoyl-2,5-diphenyl-pyridazin-3-one结构式
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常用名 | 6-benzoyl-2,5-diphenyl-pyridazin-3-one | 英文名 | 6-benzoyl-2,5-diphenyl-pyridazin-3-one |
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| CAS号 | 75872-31-0 | 分子量 | 352.38500 | |
| 密度 | 1.17g/cm3 | 沸点 | 533.1ºC at 760 mmHg | |
| 分子式 | C23H16N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 276.2ºC |
| 英文名 | 6-benzoyl-2,5-diphenylpyridazin-3-one |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.17g/cm3 |
|---|---|
| 沸点 | 533.1ºC at 760 mmHg |
| 分子式 | C23H16N2O2 |
| 分子量 | 352.38500 |
| 闪点 | 276.2ºC |
| 精确质量 | 352.12100 |
| PSA | 51.96000 |
| LogP | 4.13050 |
| InChIKey | SRDKDQFRXJKIOF-UHFFFAOYSA-N |
| SMILES | O=C(c1ccccc1)c1nn(-c2ccccc2)c(=O)cc1-c1ccccc1 |
| 折射率 | 1.635 |
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~91%
6-benzoyl-2,5-d... 75872-31-0 |
| 文献:Bestmann, Hans Juergen; Schmid, Guenter; Sandmeier, Dieter Tetrahedron Letters, 1980 , vol. 21, p. 2939 - 2942 |
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~%
6-benzoyl-2,5-d... 75872-31-0 |
| 文献:Patel; Vyas; Pandey; Tavares; Fernandes Synthetic Communications, 1991 , vol. 21, # 8-9 p. 1021 - 1026 |
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~%
6-benzoyl-2,5-d... 75872-31-0 |
| 文献:Patel; Vyas; Pandey; Tavares; Fernandes Synthetic Communications, 1991 , vol. 21, # 18-19 p. 1935 - 1940 |
| 6-benzoyl-2,5-diphenyl-pyridazin-3-one上游产品 4 | |
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| 6-benzoyl-2,5-diphenyl-pyridazin-3-one下游产品 0 | |
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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: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-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:Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation M...
来源:Broad Institute
靶标:N/A
External Id:2146-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Confirmatory qHTS for agonist of cAMP-regulated guanine nucleotide exchange factor 3 ...
来源:NCGC
External Id:epac1-activator-f1f2f3f4
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实验名称:Confirmatory qHTS for antagonist of cAMP-regulated guanine nucleotide exchange factor...
来源:NCGC
External Id:epac1-inhibitor-f1f2f3f4
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| 6-Benzoyl-2,5-diphenyl-3(2H)-pyridazinon |