N-(6-amino-3-methyl-2,4-dioxo-1-propyl-1,2,3,4-tetrahydropyrimidine-5-carbothioyl)cyclopropanecarboxamide结构式
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常用名 | N-(6-amino-3-methyl-2,4-dioxo-1-propyl-1,2,3,4-tetrahydropyrimidine-5-carbothioyl)cyclopropanecarboxamide | 英文名 | N-(6-amino-3-methyl-2,4-dioxo-1-propyl-1,2,3,4-tetrahydropyrimidine-5-carbothioyl)cyclopropanecarboxamide |
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| CAS号 | 796103-19-0 | 分子量 | 310.37 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C13H18N4O3S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | N-(6-amino-3-methyl-2,4-dioxo-1-propyl-1,2,3,4-tetrahydropyrimidine-5-carbothioyl)cyclopropanecarboxamide |
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| 分子式 | C13H18N4O3S |
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| 分子量 | 310.37 |
| InChIKey | BYQHYIAVLJVXKE-UHFFFAOYSA-N |
| SMILES | CCCN1C(=C(C(=O)N(C1=O)C)C(=S)NC(=O)C2CC2)N |
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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
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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
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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
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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
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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
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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
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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
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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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实验名称:Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition
来源:Southern Research Specialized Biocontainment Screening Center
靶标:Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocysteine
External Id:CEGtase_01
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