2-(吡啶-4-基)苯并[d]噁唑-5-胺结构式
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常用名 | 2-(吡啶-4-基)苯并[d]噁唑-5-胺 | 英文名 | 2-(Pyridin-4-yl)benzo[d]oxazol-5-amine |
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| CAS号 | 349609-85-4 | 分子量 | 211.21900 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C12H9N3O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 2-吡啶-4-苯并噁唑-5-胺 |
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| 英文名 | 2-pyridin-4-yl-1,3-benzoxazol-5-amine |
| 英文别名 | 更多 |
| 分子式 | C12H9N3O |
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| 分子量 | 211.21900 |
| 精确质量 | 211.07500 |
| PSA | 64.94000 |
| LogP | 3.05320 |
| InChIKey | ZCTHPTXYNUMPGE-UHFFFAOYSA-N |
| SMILES | Nc1ccc2oc(-c3ccncc3)nc2c1 |
| 储存条件 | 2-8°C |
| 海关编码 | 2934999090 |
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~85%
2-(吡啶-4-基)苯并[d]... 349609-85-4 |
| 文献:BRANDEIS UNIVERSITY; THE BRIGHAM AND WOMEN'S HOSPITAL, INC.; HEDSTROM, Lizbeth, K.; CUNY, Gregory, D.; GORLA, Suresh, Kumar; KAVITHA, Mandapati Patent: WO2014/28931 A2, 2014 ; Location in patent: Page/Page column 139 ; |
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2-(吡啶-4-基)苯并[d]... 349609-85-4 |
| 文献:BRANDEIS UNIVERSITY; THE BRIGHAM AND WOMEN'S HOSPITAL, INC.; HEDSTROM, Lizbeth, K.; CUNY, Gregory, D.; GORLA, Suresh, Kumar; KAVITHA, Mandapati Patent: WO2014/28931 A2, 2014 ; |
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2-(吡啶-4-基)苯并[d]... 349609-85-4 |
| 文献:Haugwitz; Angel; Jacobs; Maurer; Narayanan; Cruthers; Szanto Journal of Medicinal Chemistry, 1982 , vol. 25, # 8 p. 969 - 974 |
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2-(吡啶-4-基)苯并[d]... 349609-85-4 |
| 文献:BRANDEIS UNIVERSITY; THE BRIGHAM AND WOMEN'S HOSPITAL, INC.; HEDSTROM, Lizbeth, K.; CUNY, Gregory, D.; GORLA, Suresh, Kumar; KAVITHA, Mandapati Patent: WO2014/28931 A2, 2014 ; |
| 2-(吡啶-4-基)苯并[d]噁唑-5-胺上游产品 4 | |
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| 2-(吡啶-4-基)苯并[d]噁唑-5-胺下游产品 0 | |
| 海关编码 | 2934999090 |
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| 中文概述 | 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途 |
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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实验名称:Inhibition of human p110alpha PI3K fragment by AlphaScreen assay
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
External Id:CHEMBL1646725
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实验名称:Inhibition of human PI3K p110beta catalytic subunit by AlphaScreen competition assay
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
External Id:CHEMBL1646726
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实验名称:Inhibition of human PI3K p110gamma catalytic subunit by AlphaScreen assay
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
External Id:CHEMBL1646727
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实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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实验名称:Inhibition of human PI3K p110delta catalytic subunit by AlphaScreen assay
来源:ChEMBL
靶标:Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
External Id:CHEMBL1646729
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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| 2-Pyridin-4-yl-benzooxazol-5-ylamine |