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1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione

更新时间:2025-08-26 09:58:22

1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione结构式
1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione结构式
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常用名 1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione 英文名 1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione
CAS号 5426-70-0 分子量 286.28600
密度 1.378g/cm3 沸点 568.9ºC at 760 mmHg
分子式 C14H14N4O3 熔点 N/A
MSDS N/A 闪点 297.9ºC

 名称

英文名 1,3-dimethyl-8-(phenoxymethyl)-7H-purine-2,6-dione
英文别名 更多

 物理化学性质

密度 1.378g/cm3
沸点 568.9ºC at 760 mmHg
分子式 C14H14N4O3
分子量 286.28600
闪点 297.9ºC
精确质量 286.10700
PSA 81.91000
LogP 0.53930
InChIKey QIQXXFPSAXJCFM-UHFFFAOYSA-N
SMILES Cn1c(=O)c2[nH]c(COc3ccccc3)nc2n(C)c1=O
折射率 1.634

 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

1,3-dimethyl-8-phenoxymethyl-3,7-dihydro-purine-2,6-dione
1,3-Dimethyl-8-phenoxymethyl-3,7-dihydro-purin-2,6-dion
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