1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺结构式
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常用名 | 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺 | 英文名 | 4-Piperidinecarboxamide,4-(ethylamino)-1-(phenylmethyl) |
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| CAS号 | 1027-91-4 | 分子量 | 261.36300 | |
| 密度 | 1.11g/cm3 | 沸点 | 432.8ºC at 760mmHg | |
| 分子式 | C15H23N3O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 215.5ºC |
| 中文名 | 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺 |
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| 英文名 | 1-benzyl-4-(ethylamino)piperidine-4-carboxamide |
| 中文别名 | 1-苄基-4-(乙基氨基)哌啶-4-羧酰胺 |
| 英文别名 | 更多 |
| 密度 | 1.11g/cm3 |
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| 沸点 | 432.8ºC at 760mmHg |
| 分子式 | C15H23N3O |
| 分子量 | 261.36300 |
| 闪点 | 215.5ºC |
| 精确质量 | 261.18400 |
| PSA | 58.36000 |
| LogP | 2.14510 |
| InChIKey | LPPPBYXGXSHYQJ-UHFFFAOYSA-N |
| SMILES | CCNC1(C(N)=O)CCN(Cc2ccccc2)CC1 |
| 蒸汽压 | 1.08E-07mmHg at 25°C |
| 折射率 | 1.577 |
| 海关编码 | 2933399090 |
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~96%
1-苯甲基-4-(乙胺基)哌啶... 1027-91-4 |
| 文献:TANABE SEIYAKU CO., LTD. Patent: WO2007/46550 A1, 2007 ; Location in patent: Page/Page column 127-128 ; WO 2007/046550 A1 |
| 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺上游产品 1 | |
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| 1-苯甲基-4-(乙胺基)哌啶-4-甲酰胺下游产品 1 | |
| 海关编码 | 2933399090 |
|---|---|
| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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: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
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| 1-Benzyl-4-ethylamino-4-carbamoyl-piperidin |
| HMS3085D05 |
| 1-Benzyl-4-carbamoyl-4-ethylamino-piperidin |
| 1-benzyl-4-carbamoyl-4-(ethylamino)piperidine |
| 1-benzyl-4-ethylamino-piperidine-4-carboxylic acid amide |