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2H-Pyrimido[4,5-e]-1,3-oxazine-6,8(5H,7H)-dione,3,4-dihydro-3-(phenylmethyl)

更新时间:2025-09-19 23:46:34

2H-Pyrimido[4,5-e]-1,3-oxazine-6,8(5H,7H)-dione,3,4-dihydro-3-(phenylmethyl)结构式
2H-Pyrimido[4,5-e]-1,3-oxazine-6,8(5H,7H)-dione,3,4-dihydro-3-(phenylmethyl)结构式
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常用名 2H-Pyrimido[4,5-e]-1,3-oxazine-6,8(5H,7H)-dione,3,4-dihydro-3-(phenylmethyl) 英文名 2H-Pyrimido[4,5-e]-1,3-oxazine-6,8(5H,7H)-dione,3,4-dihydro-3-(phenylmethyl)
CAS号 13365-47-4 分子量 259.26100
密度 1.41g/cm3 沸点 519.7ºC at 760mmHg
分子式 C13H13N3O3 熔点 N/A
MSDS N/A 闪点 268.1ºC

 名称

英文名 3-benzyl-4,5-dihydro-2H-pyrimido[4,5-e][1,3]oxazine-6,8-dione
英文别名 更多

 物理化学性质

密度 1.41g/cm3
沸点 519.7ºC at 760mmHg
分子式 C13H13N3O3
分子量 259.26100
闪点 268.1ºC
精确质量 259.09600
PSA 78.19000
LogP 0.35320
InChIKey ZUOWTNICPAEGMJ-UHFFFAOYSA-N
SMILES O=c1[nH]c2c(c(=O)[nH]1)OCN(Cc1ccccc1)C2
蒸汽压 2.03E-11mmHg at 25°C
折射率 1.662

 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

3-benzyl-3,4-dihydro-2h-pyrimido[4,5-e][1,3]oxazine-6,8(5h,7h)-dione
3-benzyl-3,4-dihydro-2H,5H-pyrimido[4,5-e][1,3]oxazine-6,8-dione
3-Benzyl-6,8-dihydroxy-3,4-dihydro-2H-pyrimido<4,5-e>-1,3-oxazin
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