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2,4,6(1H,3H,5H)-Pyrimidinetrione,1,3-dimethyl-5-(phenylmethyl)

更新时间:2025-08-25 17:01:11

2,4,6(1H,3H,5H)-Pyrimidinetrione,1,3-dimethyl-5-(phenylmethyl)结构式
2,4,6(1H,3H,5H)-Pyrimidinetrione,1,3-dimethyl-5-(phenylmethyl)结构式
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常用名 2,4,6(1H,3H,5H)-Pyrimidinetrione,1,3-dimethyl-5-(phenylmethyl) 英文名 2,4,6(1H,3H,5H)-Pyrimidinetrione,1,3-dimethyl-5-(phenylmethyl)
CAS号 15018-52-7 分子量 246.26200
密度 1.254g/cm3 沸点 360ºC at 760mmHg
分子式 C13H14N2O3 熔点 N/A
MSDS N/A 闪点 154.4ºC

 名称

英文名 5-benzyl-1,3-dimethyl-1,3-diazinane-2,4,6-trione
英文别名 更多

 物理化学性质

密度 1.254g/cm3
沸点 360ºC at 760mmHg
分子式 C13H14N2O3
分子量 246.26200
闪点 154.4ºC
精确质量 246.10000
PSA 57.69000
LogP 0.77150
InChIKey JOBKZALYQYGIAA-UHFFFAOYSA-N
SMILES CN1C(=O)C(Cc2ccccc2)C(=O)N(C)C1=O
蒸汽压 2.29E-05mmHg at 25°C
折射率 1.571

 毒性和生态

 合成线路

 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: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
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:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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 英文别名

5-benzyl-1,3-dimethyl-barbituric acid
1,3-dimethyl-5-benzyl-5-cytisylmethylbarbituric acid
5-benzyl-1,3-dimethyl-pyrimidine-2,4,6-trione
BARBITURIC ACID,5-BENZYL-1,3-DIMETHYL
5-Benzyl-1,3-dimethyl-barbitursaeure
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