2-hydroxy-3-(2-hydroxy-4-oxo-chromen-3-yl)sulfanyl-chromen-4-one结构式
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常用名 | 2-hydroxy-3-(2-hydroxy-4-oxo-chromen-3-yl)sulfanyl-chromen-4-one | 英文名 | 2-hydroxy-3-(2-hydroxy-4-oxo-chromen-3-yl)sulfanyl-chromen-4-one |
|---|---|---|---|---|
| CAS号 | 1821-13-2 | 分子量 | 354.33300 | |
| 密度 | 1.67g/cm3 | 沸点 | 470.8ºC at 760mmHg | |
| 分子式 | C18H10O6S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 238.5ºC |
| 英文名 | 4-hydroxy-3-(4-hydroxy-2-oxochromen-3-yl)sulfanylchromen-2-one |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.67g/cm3 |
|---|---|
| 沸点 | 470.8ºC at 760mmHg |
| 分子式 | C18H10O6S |
| 分子量 | 354.33300 |
| 闪点 | 238.5ºC |
| 精确质量 | 354.02000 |
| PSA | 126.18000 |
| LogP | 3.46180 |
| InChIKey | JHLUHYNVTIYAKS-UHFFFAOYSA-N |
| SMILES | O=c1oc2ccccc2c(O)c1Sc1c(O)c2ccccc2oc1=O |
| 蒸汽压 | 1.15E-09mmHg at 25°C |
| 折射率 | 1.784 |
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2-hydroxy-3-(2-... 1821-13-2 |
| 文献:Eisenhauer; Link Journal of the American Chemical Society, 1954 , vol. 76, p. 1647 |
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~%
2-hydroxy-3-(2-... 1821-13-2 |
| 文献:Eisenhauer; Link Journal of the American Chemical Society, 1954 , vol. 76, p. 1647 |
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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: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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
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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:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
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| A 1062 |
| HMS3078J18 |
| 4,4'-dihydroxy-3,3'-sulfanediyl-bis-chromen-2-one |