4,6-双(甲基硫代)嘧啶结构式
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常用名 | 4,6-双(甲基硫代)嘧啶 | 英文名 | Pyrimidine,4,6-bis(methylthio) |
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| CAS号 | 1450-90-4 | 分子量 | 172.27100 | |
| 密度 | 1.26g/cm3 | 沸点 | 294.5ºC at 760mmHg | |
| 分子式 | C6H8N2S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 131.9ºC |
| 中文名 | 4,6-双(甲基硫代)嘧啶 |
|---|---|
| 英文名 | 4,6-bis(methylsulfanyl)pyrimidine |
| 英文别名 | 更多 |
| 密度 | 1.26g/cm3 |
|---|---|
| 沸点 | 294.5ºC at 760mmHg |
| 分子式 | C6H8N2S2 |
| 分子量 | 172.27100 |
| 闪点 | 131.9ºC |
| 精确质量 | 172.01300 |
| PSA | 76.38000 |
| LogP | 1.92040 |
| InChIKey | PDEXXTHEMNGLQV-UHFFFAOYSA-N |
| SMILES | CSc1cc(SC)ncn1 |
| 蒸汽压 | 0.00284mmHg at 25°C |
| 折射率 | 1.615 |
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4,6-双(甲基硫代)嘧啶 1450-90-4 |
| 文献:IRM LLC; NOVARTIS AG Patent: WO2008/42639 A1, 2008 ; Location in patent: Page/Page column 69 ; WO 2008/042639 A1 |
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4,6-双(甲基硫代)嘧啶 1450-90-4 |
| 文献:Porter, John R; Archibald, Sarah C; Brown, Julien A; Childs, Kirstie; Critchley, David; Head, John C; Hutchinson, Brian; Parton, Ted A H; Robinson, Martyn K; Shock, Anthony; Warrellow, Graham J; Zomaya, Alex Bioorganic and medicinal chemistry letters, 2002 , vol. 12, # 12 p. 1595 - 1598 |
| 4,6-双(甲基硫代)嘧啶上游产品 2 | |
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| 4,6-双(甲基硫代)嘧啶下游产品 0 | |
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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: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
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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: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: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
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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: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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| 4,6-Bis-methylmercapto-pyrimidin |
| 4,6-bis-methylsulfanyl-pyrimidine |