10,10-二甲基蒽酮结构式
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常用名 | 10,10-二甲基蒽酮 | 英文名 | Melitracen hydrochloride |
|---|---|---|---|---|
| CAS号 | 5447-86-9 | 分子量 | 222.282 | |
| 密度 | 1.1±0.1 g/cm3 | 沸点 | 346.6±22.0 °C at 760 mmHg | |
| 分子式 | C16H14O | 熔点 | 101-103ºC | |
| MSDS | N/A | 闪点 | 149.4±17.3 °C |
| 中文名 | 10,10-二甲基蒽酮 |
|---|---|
| 英文名 | 10,10-Dimethylanthrone |
| 英文别名 | 更多 |
| 密度 | 1.1±0.1 g/cm3 |
|---|---|
| 沸点 | 346.6±22.0 °C at 760 mmHg |
| 熔点 | 101-103ºC |
| 分子式 | C16H14O |
| 分子量 | 222.282 |
| 闪点 | 149.4±17.3 °C |
| 精确质量 | 222.104462 |
| PSA | 17.07000 |
| LogP | 4.61 |
| InChIKey | GWFCYDIAPRIMLA-UHFFFAOYSA-N |
| SMILES | CC1(C)c2ccccc2C(=O)c2ccccc21 |
| 蒸汽压 | 0.0±0.8 mmHg at 25°C |
| 折射率 | 1.590 |
| 储存条件 | 2-8°C |
| 计算化学 | 1.疏水参数计算参考值(XlogP):无 2.氢键供体数量:0 3.氢键受体数量:1 4.可旋转化学键数量:0 5.互变异构体数量:无 6.拓扑分子极性表面积:17.1 7.重原子数量:17 8.表面电荷:0 9.复杂度:290 10.同位素原子数量:0 11.确定原子立构中心数量:0 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 海关编码 | 2914399090 |
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| 10,10-二甲基蒽酮上游产品 9 | |
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| 10,10-二甲基蒽酮下游产品 5 | |
| 海关编码 | 2914399090 |
|---|---|
| 中文概述 | 2914399090. 其他不含其他含氧基的芳香酮. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:5.5%. 普通关税:30.0% |
| 申报要素 | 品名, 成分含量, 用途, 丙酮报明包装 |
| Summary | 2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
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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: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: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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| 10,10-dimethylanthracen-9-one |
| 10,10-Dimethylanthracen-9(10H)-on |
| 10,10-Dimethyl-9(10H)-anthracenone |
| 10,10-dimethylanthracen-9(10H)-one |
| Melitracen hydrochloride |