[2-[6-(benzoyloxymethyl)-5-hydroxy-2-phenyl-1,3-dioxan-4-yl]-2-hydroxy-ethyl] benzoate结构式
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常用名 | [2-[6-(benzoyloxymethyl)-5-hydroxy-2-phenyl-1,3-dioxan-4-yl]-2-hydroxy-ethyl] benzoate | 英文名 | [2-[6-(benzoyloxymethyl)-5-hydroxy-2-phenyl-1,3-dioxan-4-yl]-2-hydroxy-ethyl] benzoate |
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| CAS号 | 7464-39-3 | 分子量 | 478.49100 | |
| 密度 | 1.298g/cm3 | 沸点 | 673.8ºC at 760 mmHg | |
| 分子式 | C27H26O8 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 226.2ºC |
| 英文名 | [6-(2-benzoyloxy-1-hydroxyethyl)-5-hydroxy-2-phenyl-1,3-dioxan-4-yl]methyl benzoate |
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| 英文别名 | 更多 |
| 密度 | 1.298g/cm3 |
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| 沸点 | 673.8ºC at 760 mmHg |
| 分子式 | C27H26O8 |
| 分子量 | 478.49100 |
| 闪点 | 226.2ºC |
| 精确质量 | 478.16300 |
| PSA | 111.52000 |
| LogP | 2.90500 |
| InChIKey | PBDQBYAPPGCVBX-UHFFFAOYSA-N |
| SMILES | O=C(OCC(O)C1OC(c2ccccc2)OC(COC(=O)c2ccccc2)C1O)c1ccccc1 |
| 折射率 | 1.598 |
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[2-[6-(benzoylo... 7464-39-3 |
| 文献:v. Vargha Chemische Berichte, 1935 , vol. 68, p. 1377,1378 |
| 上游产品 2 | |
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| 下游产品 0 | |
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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: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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实验名称:Identification of agents that induce E-selectin on human endothelial cells Measured i...
来源:Broad Institute
靶标:E-Selectin
External Id:2152-01_Activator_SinglePoint_HTS_Activity
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| 1,6-di-O-benzoyl-2,4-O-benzylidene-D-glucitol |