6H-Indolo[2,3-b]quinoxaline,9-nitro结构式
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常用名 | 6H-Indolo[2,3-b]quinoxaline,9-nitro | 英文名 | 6H-Indolo[2,3-b]quinoxaline,9-nitro |
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| CAS号 | 57743-37-0 | 分子量 | 264.23900 | |
| 密度 | 1.569g/cm3 | 沸点 | 571ºC at 760mmHg | |
| 分子式 | C14H8N4O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 299.1ºC |
| 英文名 | 9-nitro-6H-indolo[3,2-b]quinoxaline |
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| 英文别名 | 更多 |
| 密度 | 1.569g/cm3 |
|---|---|
| 沸点 | 571ºC at 760mmHg |
| 分子式 | C14H8N4O2 |
| 分子量 | 264.23900 |
| 闪点 | 299.1ºC |
| 精确质量 | 264.06500 |
| PSA | 87.39000 |
| LogP | 3.69570 |
| InChIKey | DVCQVUGEZJGWFY-UHFFFAOYSA-N |
| SMILES | O=[N+]([O-])c1ccc2[nH]c3nc4ccccc4nc3c2c1 |
| 折射率 | 1.877 |
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~61%
6H-Indolo[2,3-b... 57743-37-0 |
| 文献:Dowlatabadi, Reza; Khalaj, Ali; Rahimian, Sima; Montazeri, Maedeh; Amini, Mohsen; Shahverdi, Ahmadreza; Mahjub, Elham Synthetic Communications, 2011 , vol. 41, # 11 p. 1650 - 1658 |
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~90%
6H-Indolo[2,3-b... 57743-37-0 |
| 文献:Sarkis; Al-Badri Journal of Heterocyclic Chemistry, 1980 , vol. 17, # 4 p. 813 - 815 |
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~15%
6H-Indolo[2,3-b... 57743-37-0 |
| 文献:Ivashchenko, A. V.; Drushlyak, A. G.; Titov, V. V. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1984 , vol. 20, # 5 p. 537 - 542 Khimiya Geterotsiklicheskikh Soedinenii, 1984 , vol. 20, # 5 p. 667 - 672 |
| 6H-Indolo[2,3-b]quinoxaline,9-nitro上游产品 3 | |
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| 6H-Indolo[2,3-b]quinoxaline,9-nitro下游产品 0 | |
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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: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: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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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| 9-nitroindolo<2,3-b>quinoxaline |