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4-(1-(4-羟基-3-甲氧基苄基)-1H-苯并[d]咪唑-2-基)-2-甲氧基苯酚

更新时间:2026-08-08 13:49:37

4-(1-(4-羟基-3-甲氧基苄基)-1H-苯并[d]咪唑-2-基)-2-甲氧基苯酚结构式
4-(1-(4-羟基-3-甲氧基苄基)-1H-苯并[d]咪唑-2-基)-2-甲氧基苯酚结构式
品牌特惠专场
常用名 4-(1-(4-羟基-3-甲氧基苄基)-1H-苯并[d]咪唑-2-基)-2-甲氧基苯酚 英文名 ATPase-IN-2
CAS号 85573-18-8 分子量 376.41
密度 N/A 沸点 N/A
分子式 C22H20N2O4 熔点 N/A
MSDS N/A 闪点 N/A

 用途


ATP酶-IN-2是一种ATP酶抑制剂,其IC50值为0.9μM。ATP酶-IN-2抑制艰难梭菌毒素B(TcdB)糖水解酶活性,AC50值为30.91μM。ATP酶-IN-2可用于ATP相关的研究[1]。

 名称

中文名 4-(1-(4-羟基-3-甲氧基苄基)-1H-苯并[d]咪唑-2-基)-2-甲氧基苯酚
英文名 4-(1-(4-Hydroxy-3-methoxybenzyl)-1H-benzo[d]imidazol-2-yl)-2-methoxyphenol
英文别名 更多

 生物活性

描述 ATP酶-IN-2是一种ATP酶抑制剂,其IC50值为0.9μM。ATP酶-IN-2抑制艰难梭菌毒素B(TcdB)糖水解酶活性,AC50值为30.91μM。ATP酶-IN-2可用于ATP相关的研究[1]。
相关类别
靶点实验

IC50: 0.9 μM (ATPase)[1]

参考文献

[1]. Jeffery Brodsky, et al. Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents. 2010.

 物理化学性质

分子式 C22H20N2O4
分子量 376.41
InChIKey SBVOOAOEAYENPN-UHFFFAOYSA-N
SMILES COc1cc(Cn2c(-c3ccc(O)c(OC)c3)nc3ccccc32)ccc1O
储存条件 -20°C

 靶点实验

查看更多实验

实验名称:C. difficile toxins: Counterscreen in absence of substrate UDPG Measured in Biochemic...
来源:Broad Institute
靶标:N/A
External Id:7074-02_Inhibitor_Dose_CherryPick_Activity
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
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: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.
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: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
实验名称:qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
来源:NCGC
External Id:tdp43-p2-repeat
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 英文别名

MFCD01952969
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