3-Pyridinecarboxamide,1,6-dihydro-6-oxo-1-b-D-ribofuranosyl

• 常用名: 3-Pyridinecarboxamide,1,6-dihydro-6-oxo-1-b-D-ribofuranosyl
• 英文名: 3-Pyridinecarboxamide,1,6-dihydro-6-oxo-1-b-D-ribofuranosyl
• CAS号: 23312-67-6
• 分子量: 270.23900
• 密度: 1.658g/cm3
• 沸点: 671.7ºC at 760mmHg
• 分子式: C₁₁H₁₄N₂O₆
• 熔点: N/A
• 闪点: 360ºC

名称

• 英文名: 1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-oxopyridine-3-carboxamide

物理化学性质

• 密度: 1.658g/cm3
• 沸点: 671.7ºC at 760mmHg
• 分子式: C₁₁H₁₄N₂O₆
• 分子量: 270.23900
• 闪点: 360ºC
• 精确质量: 270.08500
• PSA: 135.01000
• InChIKey: NCAHRPOFSWUZKN-UHFFFAOYSA-N
• SMILES: NC(=O)c1ccc(=O)n(C2OC(CO)C(O)C2O)c1
• 蒸汽压: 6.45E-21mmHg at 25°C
• 折射率: 1.679

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：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

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英文别名

• HMS3086A23
• 6-oxo-1-pentofuranosyl-1,6-dihydropyridine-3-carboxamide