5H-Thiazolo[3,2-a]pyrimidine-5,7(6H)-dione,2,3-dihydro

• 常用名: 5H-Thiazolo[3,2-a]pyrimidine-5,7(6H)-dione,2,3-dihydro
• 英文名: 5H-Thiazolo[3,2-a]pyrimidine-5,7(6H)-dione,2,3-dihydro
• CAS号: 72211-55-3
• 分子量: 170.18900
• 密度: 1.76g/cm3
• 沸点: 300.1ºC at 760mmHg
• 分子式: C₆H₆N₂O₂S
• 熔点: N/A
• 闪点: 135.3ºC

名称

• 英文名: 2,3-dihydro-[1,3]thiazolo[3,2-a]pyrimidine-5,7-dione

物理化学性质

• 密度: 1.76g/cm3
• 沸点: 300.1ºC at 760mmHg
• 分子式: C₆H₆N₂O₂S
• 分子量: 170.18900
• 闪点: 135.3ºC
• 精确质量: 170.01500
• PSA: 75.04000
• InChIKey: PWVGKYQTRHJBIL-UHFFFAOYSA-N
• SMILES: O=C1CC(=O)N2CCSC2=N1
• 折射率: 1.808

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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英文别名

• 2,3-dihydrothiazolo<3,2-a>pyrimidine-5,7-dione
• HMS3087I23
• 7-Hydroxy-2,3,4,5-Tetrahydrothiazolo<3,2-a>Pyrimidin-5-on