6-氟-4-羟基喹啉-3-甲酸结构式
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常用名 | 6-氟-4-羟基喹啉-3-甲酸 | 英文名 | 6-Fluoro-4-hydroxyquinoline-3-carboxylic acid |
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| CAS号 | 343-10-2 | 分子量 | 207.158 | |
| 密度 | 1.6±0.1 g/cm3 | 沸点 | 387.8±42.0 °C at 760 mmHg | |
| 分子式 | C10H6FNO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 188.4±27.9 °C |
| 中文名 | 4-羟基-6-氟喹啉-3-甲酸 |
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| 英文名 | 6-fluoro-4-hydroxyquinoline-3-carboxylic acid |
| 中文别名 | 6-氟-4-羟基喹啉-3-甲酸 | 6-氟-4-羟基喹啉-3-羧酸 |
| 英文别名 | 更多 |
| 密度 | 1.6±0.1 g/cm3 |
|---|---|
| 沸点 | 387.8±42.0 °C at 760 mmHg |
| 分子式 | C10H6FNO3 |
| 分子量 | 207.158 |
| 闪点 | 188.4±27.9 °C |
| 精确质量 | 207.033173 |
| PSA | 70.42000 |
| LogP | 3.52 |
| 蒸汽压 | 0.0±0.9 mmHg at 25°C |
| 折射率 | 1.700 |
| 储存条件 | 室温,密封,干燥 |
| 危害码 (欧洲) | Xi: Irritant; |
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| 海关编码 | 2933499090 |
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6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Journal of Medicinal Chemistry, , vol. 49, # 22 p. 6443 - 6450 |
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~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Heterocycles, , vol. 51, # 10 p. 2377 - 2384 |
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~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Journal of Medicinal Chemistry, , vol. 49, # 22 p. 6443 - 6450 |
|
~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Heterocycles, , vol. 51, # 10 p. 2377 - 2384 |
|
~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Heterocycles, , vol. 51, # 10 p. 2377 - 2384 |
|
~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Heterocycles, , vol. 51, # 10 p. 2377 - 2384 |
|
~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Heterocycles, , vol. 51, # 10 p. 2377 - 2384 |
|
~%
6-氟-4-羟基喹啉-3-甲酸 343-10-2 |
| 文献:Journal of Medicinal Chemistry, , vol. 49, # 22 p. 6443 - 6450 |
| 6-氟-4-羟基喹啉-3-甲酸上游产品 5 | |
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| 6-氟-4-羟基喹啉-3-甲酸下游产品 2 | |
| 海关编码 | 2933499090 |
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| 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: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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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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: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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| 3-Carboxy-6-fluoro-4-hydroxyquinoline |
| 3-Quinolinecarboxylic acid,6-fluoro-4-hydroxy |
| MFCD00973836 |
| 3-quinolinecarboxylic acid,6-fluoro-1,4-dihydro-4-oxo |
| 6-Fluor-4-hydroxy-chinolin-3-carbonsaeure |
| 6-Fluoro-4-hydroxyquinoline-3-carboxylic acid |
| 4-hydroxy-6-fluoro-3-quinoline carboxylic acid |
| 6-Fluoro-4-hydroxy-quinoline-3-carboxylic acid |
| 6-fluoro-4-hydroxyquinoline-3-carboxylic acid(SALTDATA: FREE) |
| 6-Fluoro-4-hydroxy-3-quinolinecarboxylic acid |
| 4-Hydroxy-6-fluoroquinoline-3-carboxylic acid |