7,9-diazaspiro[4.5]decane-6,8,10-trione

• 常用名: 7,9-diazaspiro[4.5]decane-6,8,10-trione
• 英文名: 7,9-diazaspiro[4.5]decane-6,8,10-trione
• CAS号: 56209-30-4
• 分子量: 182.17700
• 密度: 1.39g/cm3
• 沸点: N/A
• 分子式: C₈H₁₀N₂O₃
• 熔点: N/A
• 闪点: N/A

7,9-diazaspiro[4.5]decane-6,8,10-trione名称

• 英文名: 7,9-diazaspiro[4.5]decane-6,8,10-trione

7,9-diazaspiro[4.5]decane-6,8,10-trione物理化学性质

• 密度: 1.39g/cm3
• 分子式: C₈H₁₀N₂O₃
• 分子量: 182.17700
• 精确质量: 182.06900
• PSA: 75.27000
• LogP: 0.57040
• InChIKey: HYPRUQJUBWRVEM-UHFFFAOYSA-N
• SMILES: O=C1NC(=O)C2(CCCC2)C(=O)N1
• 折射率: 1.565

7,9-diazaspiro[4.5]decane-6,8,10-trione靶点实验

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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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7,9-diazaspiro[4.5]decane-6,8,10-trione英文别名

• 5,5-Tetramethylen-barbitursaeure
• spirocyclopentane-1',5-barbituric acid
• HMS3094E15
• 5,5-Tetramethylenebarbituric acid