1-异喹啉羧酰胺结构式
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常用名 | 1-异喹啉羧酰胺 | 英文名 | 1-Isoquinolinecarboxamide |
|---|---|---|---|---|
| CAS号 | 1436-44-8 | 分子量 | 172.18300 | |
| 密度 | 1.27g/cm3 | 沸点 | 440.9ºC at 760mmHg | |
| 分子式 | C10H8N2O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 220.4ºC |
| 中文名 | 1-异喹啉羧酰胺 |
|---|---|
| 英文名 | isoquinoline-1-carboxamide |
| 英文别名 | 更多 |
| 密度 | 1.27g/cm3 |
|---|---|
| 沸点 | 440.9ºC at 760mmHg |
| 分子式 | C10H8N2O |
| 分子量 | 172.18300 |
| 闪点 | 220.4ºC |
| 精确质量 | 172.06400 |
| PSA | 55.98000 |
| LogP | 2.03400 |
| InChIKey | YZDXFUGIDTUCDA-UHFFFAOYSA-N |
| SMILES | NC(=O)c1nccc2ccccc12 |
| 蒸汽压 | 5.7E-08mmHg at 25°C |
| 折射率 | 1.678 |
| 海关编码 | 2933499090 |
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~84%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Jones, Raymond C. F.; Smallridge, Mark J.; Chapleo, Christopher B. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1990 , # 2 p. 385 - 391 |
|
~99%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Minisci, Francesco; Citterio, Attilio; Vismara, Elena; Giordano, Claudio Tetrahedron, 1985 , vol. 41, # 19 p. 4157 - 4170 |
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~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Reissert Chemische Berichte, 1905 , vol. 38, p. 3432 |
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~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Langry, Kevin C. Organic Preparations and Procedures International, 1994 , vol. 26, # 4 p. 429 - 438 |
|
~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Langry, Kevin C. Organic Preparations and Procedures International, 1994 , vol. 26, # 4 p. 429 - 438 |
|
~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Jones, Raymond C. F.; Smallridge, Mark J.; Chapleo, Christopher B. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1990 , # 2 p. 385 - 391 |
|
~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Reissert Chemische Berichte, 1905 , vol. 38, p. 3432 |
|
~%
1-异喹啉羧酰胺 1436-44-8 |
| 文献:Zincke; Krollpfeiffer Justus Liebigs Annalen der Chemie, 1915 , vol. 408, p. 332 |
| 海关编码 | 2933499090 |
|---|---|
| 中文概述 | 2933499090. 其他含喹琳或异喹啉环系的化合物〔但未进一步稠合的〕. 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 | 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. 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: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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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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| 1-Isoquinolinecarboxamide |
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| 1-isoquinaldamide |
| Isoquinaldamide |