Quinoxaline,1,4-dibenzoyl-1,2,3,4-tetrahydro- (6CI,8CI,9CI)

• 常用名: Quinoxaline,1,4-dibenzoyl-1,2,3,4-tetrahydro- (6CI,8CI,9CI)
• 英文名: Quinoxaline,1,4-dibenzoyl-1,2,3,4-tetrahydro- (6CI,8CI,9CI)
• CAS号: 22397-80-4
• 分子量: 342.39100
• 密度: 1.256g/cm3
• 沸点: 533.9ºC at 760mmHg
• 分子式: C₂₂H₁₈N₂O₂
• 熔点: N/A
• 闪点: 240.9ºC

名称

• 英文名: (4-benzoyl-2,3-dihydroquinoxalin-1-yl)-phenylmethanone

物理化学性质

• 密度: 1.256g/cm3
• 沸点: 533.9ºC at 760mmHg
• 分子式: C₂₂H₁₈N₂O₂
• 分子量: 342.39100
• 闪点: 240.9ºC
• 精确质量: 342.13700
• PSA: 40.62000
• LogP: 4.12380
• InChIKey: LASLFMMIPCCRAS-UHFFFAOYSA-N
• SMILES: O=C(c1ccccc1)N1CCN(C(=O)c2ccccc2)c2ccccc21
• 蒸汽压: 1.78E-11mmHg at 25°C
• 折射率: 1.657

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

• 2,3-dihydroquinoxaline-1,4-diylbis(phenylmethanone)
• HMS3092A23
• 1,4-Dibenzoyl-1,2,3,4-tetrahydrochinoxalin
• 1,4-dibenzoyl-1,2,3,4-tetrahydroquinoxaline