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(5E)-5-(2-溴亚苄基)-2-疏基-1,3-噻唑-4(5H)-酮

更新时间:2025-09-18 20:12:29

(5E)-5-(2-溴亚苄基)-2-疏基-1,3-噻唑-4(5H)-酮结构式
(5E)-5-(2-溴亚苄基)-2-疏基-1,3-噻唑-4(5H)-酮结构式
品牌特惠专场
常用名 (5E)-5-(2-溴亚苄基)-2-疏基-1,3-噻唑-4(5H)-酮 英文名 4-Thiazolidinone,5-[(2-bromophenyl)methylene]-2-thioxo
CAS号 5503-75-3 分子量 300.19500
密度 N/A 沸点 N/A
分子式 C10H6BrNOS2 熔点 N/A
MSDS N/A 闪点 N/A

 名称

中文名 (5E)-5-(2-溴亚苄基)-2-疏基-1,3-噻唑-4(5H)-酮
英文名 5-[(2-bromophenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one
英文别名 更多

 物理化学性质

分子式 C10H6BrNOS2
分子量 300.19500
精确质量 298.90700
PSA 86.49000
LogP 3.26670
InChIKey HCQIPSCNDYWABJ-UHFFFAOYSA-N
SMILES O=C1NC(=S)SC1=Cc1ccccc1Br

 上下游产品

上游产品  2

下游产品  0

 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:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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 英文别名

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