3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol结构式
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常用名 | 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol | 英文名 | NCGC00029283 |
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| CAS号 | 714240-31-0 | 分子量 | 337.305 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 576.7±60.0 °C at 760 mmHg | |
| 分子式 | C18H12FN3O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 302.6±32.9 °C |
用途NCGC00029283是一种werner综合征解旋酶核酸酶(WRN)解旋酶抑制剂,WRN、BLM和FANJ解旋酶的IC50分别为2.3μM、12.5μM和3.4μM[1]。 |
| 中文名 | 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol |
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| 英文名 | 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol |
| 英文别名 | 更多 |
| 描述 | NCGC00029283是一种werner综合征解旋酶核酸酶(WRN)解旋酶抑制剂,WRN、BLM和FANJ解旋酶的IC50分别为2.3μM、12.5μM和3.4μM[1]。 |
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| 相关类别 | |
| 体外研究 | NCGC00029283(0-100μM;24-72小时)有效阻止U2-OS细胞的细胞增殖[1]。细胞增殖试验[1]细胞系:U2-OS细胞浓度:1μM、10μM、100μM培养时间:24小时、48小时、72小时结果:U2-OS细胞增殖减少。 |
| 参考文献 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 576.7±60.0 °C at 760 mmHg |
| 分子式 | C18H12FN3O3 |
| 分子量 | 337.305 |
| 闪点 | 302.6±32.9 °C |
| 精确质量 | 337.086273 |
| LogP | 5.61 |
| InChIKey | FJQADEHMIMENRE-UHFFFAOYSA-N |
| SMILES | COc1ccc2[nH]c(=O)c(-c3noc(-c4ccc(F)cc4)n3)cc2c1 |
| 外观性状 | 固体 |
| 蒸汽压 | 0.0±1.7 mmHg at 25°C |
| 折射率 | 1.647 |
| 储存条件 | 2-8°C,密封,干燥 |
| 危害码 (欧洲) | Xi |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
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靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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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: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:NCATS Parallel Artificial Membrane Permeability Assay (PAMPA) Profiling
来源:NCGC
靶标:N/A
External Id:ADME-PAMPA1
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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| 3-[5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl]-6-methoxy-2(1H)-quinolinone |
| 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol |