4,5-Diphenyl-2-imidazolidinone结构式
|
常用名 | 4,5-Diphenyl-2-imidazolidinone | 英文名 | 4,5-Diphenyl-2-imidazolidinone |
|---|---|---|---|---|
| CAS号 | 100820-83-5 | 分子量 | 238.28400 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C15H14N2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 4,5-diphenylimidazolidin-2-one |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C15H14N2O |
|---|---|
| 分子量 | 238.28400 |
| 精确质量 | 238.11100 |
| PSA | 44.62000 |
| LogP | 2.75060 |
| InChIKey | MLAJDFOBMYBISF-UHFFFAOYSA-N |
| SMILES | O=C1NC(c2ccccc2)C(c2ccccc2)N1 |
|
~79%
4,5-Diphenyl-2-... 100820-83-5 |
| 文献:Hammouda, Hamdy Ali; Abd-Allah, Sanaa Osman; Zoorob, Hanafi Hassan Acta Chimica Hungarica, 1985 , vol. 119, # 1 p. 49 - 56 |
|
~%
4,5-Diphenyl-2-... 100820-83-5 |
| 文献:Biltz Justus Liebigs Annalen der Chemie, 1912 , vol. 391, p. 182 |
| 4,5-Diphenyl-2-imidazolidinone上游产品 1 | |
|---|---|
| 4,5-Diphenyl-2-imidazolidinone下游产品 2 | |
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
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
|
|
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
|
|
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
|
|
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
|
|
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
|
| 4,5-diphenyl-imidazolidin-2-one |
| 4,5-Diphenyl-imidazolidon-2 |
| 4,5-diphenylimidazolidone |
| 4,5-Diphenyl-imidazolidin-2-on |
| 4,5-Diphenyl-2-imidazolidinone |