6H-Indolo[2,3-b]quinoxaline, 6-acetyl结构式
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常用名 | 6H-Indolo[2,3-b]quinoxaline, 6-acetyl | 英文名 | 6H-Indolo[2,3-b]quinoxaline, 6-acetyl |
|---|---|---|---|---|
| CAS号 | 13860-54-3 | 分子量 | 261.27800 | |
| 密度 | 1.35g/cm3 | 沸点 | 430.9ºC at 760 mmHg | |
| 分子式 | C16H11N3O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 214.4ºC |
| 英文名 | 1-indolo[3,2-b]quinoxalin-6-ylethanone |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.35g/cm3 |
|---|---|
| 沸点 | 430.9ºC at 760 mmHg |
| 分子式 | C16H11N3O |
| 分子量 | 261.27800 |
| 闪点 | 214.4ºC |
| 精确质量 | 261.09000 |
| PSA | 47.78000 |
| LogP | 3.39780 |
| InChIKey | VOKVXGKRVFYGLA-UHFFFAOYSA-N |
| SMILES | CC(=O)n1c2ccccc2c2nc3ccccc3nc21 |
| 蒸汽压 | 1.25E-07mmHg at 25°C |
| 折射率 | 1.728 |
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~16%
6H-Indolo[2,3-b... 13860-54-3 |
| 文献:Alphonse, France-Aimee; Routier, Sylvain; Coudert, Gerard; Merour, Jean-Yves Heterocycles, 2001 , vol. 55, # 5 p. 925 - 940 |
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~%
6H-Indolo[2,3-b... 13860-54-3 |
| 文献:Alphonse, France-Aimee; Routier, Sylvain; Coudert, Gerard; Merour, Jean-Yves Heterocycles, 2001 , vol. 55, # 5 p. 925 - 940 |
| 6H-Indolo[2,3-b]quinoxaline, 6-acetyl上游产品 3 | |
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| 6H-Indolo[2,3-b]quinoxaline, 6-acetyl下游产品 1 | |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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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:qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2
来源:NCGC
靶标:eyes absent homolog 2 isoform a [Homo sapiens]
External Id:EYA2477
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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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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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:Primary cell-based high-throughput screening for identification of compounds that all...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_AlloAgonist_Primary
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实验名称:Primary cell-based high-throughput screening for identification of compounds that ant...
来源:Johns Hopkins Ion Channel Center
靶标:MAS-related GPR member X1 [Homo sapiens]
External Id:JHICC_MrgX1_Antagonist_Primary
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| 1-(6H-indolo[2,3-b]quinoxalin-6-yl)ethanone |
| 6-Acetyl-6-indolo[2,3-b]quinoxaline |
| 6H-Indolo[2,3-b]quinoxaline,6-acetyl |
| 1-Indolo[2,3-b]quinoxalin-6-yl-ethanone |
| 6-acetyl-6H-indolo[2,3-b]quinoxaline |