3-(1,3-dithian-2-yl)pyridine结构式
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常用名 | 3-(1,3-dithian-2-yl)pyridine | 英文名 | 3-(1,3-dithian-2-yl)pyridine |
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| CAS号 | 74954-95-3 | 分子量 | 197.32000 | |
| 密度 | 1.211g/cm3 | 沸点 | 352.1ºC at 760 mmHg | |
| 分子式 | C9H11NS2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 166.8ºC |
| 英文名 | 3-(1,3-dithian-2-yl)pyridine |
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| 英文别名 | 更多 |
| 密度 | 1.211g/cm3 |
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| 沸点 | 352.1ºC at 760 mmHg |
| 分子式 | C9H11NS2 |
| 分子量 | 197.32000 |
| 闪点 | 166.8ºC |
| 精确质量 | 197.03300 |
| PSA | 63.49000 |
| LogP | 2.95030 |
| InChIKey | AXNCOQBNSRCGQR-UHFFFAOYSA-N |
| SMILES | c1cncc(C2SCCCS2)c1 |
| 折射率 | 1.621 |
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~97%
3-(1,3-dithian-... 74954-95-3 |
| 文献:Shaterian, Hamid Reza; Azizi, Kobra; Fahimi, Nafiseh Journal of Sulfur Chemistry, 2011 , vol. 32, # 1 p. 85 - 91 |
| 3-(1,3-dithian-2-yl)pyridine上游产品 2 | |
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| 3-(1,3-dithian-2-yl)pyridine下游产品 1 | |
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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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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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: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:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
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| 3-(1,3-dithian-2-yl)-pyridine |
| HMS1440C05 |
| 2-(3-pyridyl)-1,3-dithiane |