前往化源商城

Anti-Influenza agent 4

更新时间:2026-08-16 08:02:05

Anti-Influenza agent 4结构式
Anti-Influenza agent 4结构式
品牌特惠专场
常用名 Anti-Influenza agent 4 英文名 Anti-Influenza agent 4
CAS号 522625-85-0 分子量 386.42
密度 N/A 沸点 N/A
分子式 C19H18N2O5S 熔点 N/A
MSDS N/A 闪点 N/A

 Anti-Influenza agent 4用途


抗流感剂4是一种有效和选择性的流感病毒抑制剂,对a/Roma和a/Parma株的EC50分别为150 nM和62 nM[1]。

 Anti-Influenza agent 4名称

英文名 Benzamide, N-[3-[[(2-furanylmethyl)amino]sulfonyl]phenyl]-4-methoxy

 Anti-Influenza agent 4生物活性

描述 抗流感剂4是一种有效和选择性的流感病毒抑制剂,对a/Roma和a/Parma株的EC50分别为150 nM和62 nM[1]。
相关类别
靶点实验

EC50: 150±0.07 nM (A/Roma), 62±0.02 nM (A/Parma)[1]

体外研究 抗流感剂4(化合物5)(0-500μM;24和48小时)在MDCK细胞中表现出低细胞毒性[1]。抗流感剂4显示出对流感毒株A/Roma和A/Parma的高度抗病毒活性,EC50分别为150±0.07 nM和62±0.02 nM[1]。在溶血抑制试验中,抗流感剂4对流感毒株A/Roma和A/Parma的IC50分别为244 nM和230.7 nM[1]。细胞毒性试验[1]细胞系:MDCK细胞浓度:0-500μM培养时间:24和48小时结果:显示出低细胞毒性,CC50值为450μM。

 Anti-Influenza agent 4物理化学性质

分子式 C19H18N2O5S
分子量 386.42
InChIKey HBZICUMXNDTDSI-UHFFFAOYSA-N
SMILES COc1ccc(C(=O)Nc2cccc(S(=O)(=O)NCc3ccco3)c2)cc1
储存条件 -20°C

 Anti-Influenza agent 4靶点实验

查看更多实验

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
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
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
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: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
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
实验名称:Absorbance-based primary biochemical high throughput screening assay to identify acti...
来源:The Scripps Research Institute Molecular Screening Center
靶标:caspase-3 preproprotein [Homo sapiens]
External Id:PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule modulators of NR3A
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1015-NR3A-Primary-Assay
共105条,当前第1页,共11页
1
2
3
4
5
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。