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3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol

更新时间:2025-08-25 18:18:30

3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol结构式
3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol结构式
品牌特惠专场
常用名 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol 英文名 NCGC00029283
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]。

 名称

中文名 3-[5-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-6-methoxy-quinolin-2-ol
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

 生物活性

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]。
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

[1]. Joshua A Sommers, et al. A high-throughput screen to identify novel small molecule inhibitors of the Werner Syndrome Helicase-Nuclease (WRN). PLoS One. 2019 Jan 9;14(1):e0210525.

 物理化学性质

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

 安全信息

危害码 (欧洲) Xi

 靶点实验

查看更多实验

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
实验名称:NCATS Kinetic Aqueous Solubility Profiling
来源:NCGC
靶标:N/A
External Id:ADME-solubility1
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来源:The Scripps Research Institute Molecular Screening Center
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External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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
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External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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
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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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.
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
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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来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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 英文别名

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
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