6,7-dimethoxyisoquinoline-1-carbaldehyde结构式
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常用名 | 6,7-dimethoxyisoquinoline-1-carbaldehyde | 英文名 | 6,7-dimethoxyisoquinoline-1-carbaldehyde |
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| CAS号 | 71046-35-0 | 分子量 | 217.22100 | |
| 密度 | 1.231g/cm3 | 沸点 | 369.4ºC at 760 mmHg | |
| 分子式 | C12H11NO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 177.2ºC |
| 英文名 | 6,7-dimethoxyisoquinoline-1-carbaldehyde |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.231g/cm3 |
|---|---|
| 沸点 | 369.4ºC at 760 mmHg |
| 分子式 | C12H11NO3 |
| 分子量 | 217.22100 |
| 闪点 | 177.2ºC |
| 精确质量 | 217.07400 |
| PSA | 48.42000 |
| LogP | 2.06450 |
| InChIKey | UHZKUBULBNDNTD-UHFFFAOYSA-N |
| SMILES | COc1cc2ccnc(C=O)c2cc1OC |
| 折射率 | 1.623 |
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~%
6,7-dimethoxyis... 71046-35-0 |
| 文献:Miles Laboratories, Inc. Patent: US4232160 A1, 1980 ; |
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~73%
6,7-dimethoxyis... 71046-35-0 |
| 文献:Batczewski, Piotr; Mallon, M. Kieran J.; Street, Jonathan D.; Joule, John A. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1990 , # 11 p. 3193 - 3198 |
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~%
6,7-dimethoxyis... 71046-35-0 |
| 文献:Postaire, E.; Martinez, D.; Viel, C.; Chastagnier, M.; Hamon, M. Bulletin de la Societe Chimique de France, 1988 , # 6 p. 982 - 988 |
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~%
6,7-dimethoxyis... 71046-35-0 |
| 文献:Postaire, E.; Martinez, D.; Viel, C.; Chastagnier, M.; Hamon, M. Bulletin de la Societe Chimique de France, 1988 , # 6 p. 982 - 988 |
| 6,7-dimethoxyisoquinoline-1-carbaldehyde上游产品 3 | |
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| 6,7-dimethoxyisoquinoline-1-carbaldehyde下游产品 2 | |
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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: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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实验名称:Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition
来源:Southern Research Specialized Biocontainment Screening Center
靶标:Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocysteine
External Id:CEGtase_01
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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实验名称:Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation M...
来源:Broad Institute
靶标:N/A
External Id:2146-01_Inhibitor_SinglePoint_HTS_Activity
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| 1-formyl 6,7-dimethoxy isoquinoline |
| 6,7-Dimethoxy-isochinolin-1-carbaldehyd |
| 6,7-dimethoxy-1-isoquinolinecarboxaldehyde |
| 6,7-dimethoxyisoquinoline-1-carboxaldehyde |
| 6,7-Dimethoxy-1-formyl-isochinolin |
| 6,7-dimethoxy-isoquinoline-1-carbaldehyde |