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5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one

更新时间:2025-09-18 10:34:33

5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one结构式
5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one结构式
委托求购
常用名 5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one 英文名 5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one
CAS号 52295-87-1 分子量 220.24800
密度 1.42g/cm3 沸点 368.3ºC at 760 mmHg
分子式 C10H8N2O2S 熔点 N/A
MSDS N/A 闪点 176.6ºC

 名称

英文名 5-phenoxy-2-sulfanylidene-1H-pyrimidin-4-one
英文别名 更多

 物理化学性质

密度 1.42g/cm3
沸点 368.3ºC at 760 mmHg
分子式 C10H8N2O2S
分子量 220.24800
闪点 176.6ºC
精确质量 220.03100
PSA 89.97000
LogP 2.22480
InChIKey RIIFDWLMPIDKQX-UHFFFAOYSA-N
SMILES O=c1[nH]c(=S)[nH]cc1Oc1ccccc1
折射率 1.692

 上下游产品

上游产品  0

下游产品  1

 靶点实验

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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: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
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 英文别名

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