2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮结构式
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常用名 | 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮 | 英文名 | 8-methylsulfanyl-9-thia-2,4,7-triazabicyclo[4.3.0]nona-2,7,10-trien-5-one |
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| CAS号 | 52948-43-3 | 分子量 | 199.25300 | |
| 密度 | 1.78g/cm3 | 沸点 | N/A | |
| 分子式 | C6H5N3OS2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 中文名 | 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮 |
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| 英文名 | 2-methylsulfanyl-6H-[1,3]thiazolo[5,4-d]pyrimidin-7-one |
| 英文别名 | 更多 |
| 密度 | 1.78g/cm3 |
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| 分子式 | C6H5N3OS2 |
| 分子量 | 199.25300 |
| 精确质量 | 198.98700 |
| PSA | 112.18000 |
| LogP | 1.10150 |
| InChIKey | LXVWBVAOOCQCIF-UHFFFAOYSA-N |
| SMILES | CSc1nc2c(=O)[nH]cnc2s1 |
| 折射率 | 1.866 |
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~99%
2-(甲基硫代)-噻唑并[5,... 52948-43-3 |
| 文献:Chattopadhyay, Gautam; Saha, Debnath; Ray, Partha Sinha; Naskar, Subhendu; Sarkar, Swarbhanu Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2010 , vol. 49, # 9 p. 1229 - 1234 |
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2-(甲基硫代)-噻唑并[5,... 52948-43-3 |
| 文献:Cook; Smith Journal of the Chemical Society, 1949 , p. 2329,2331 |
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2-(甲基硫代)-噻唑并[5,... 52948-43-3 |
| 文献:Cook; Smith Journal of the Chemical Society, 1949 , p. 2329,2331 |
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2-(甲基硫代)-噻唑并[5,... 52948-43-3 |
| 文献:Sen,A.K.; Chattopadhyay,G. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1979 , vol. 18, p. 307 - 311 |
| 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮上游产品 3 | |
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| 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮下游产品 5 | |
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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:Counterscreen for inhibitors of 5-meCpG-binding domain protein 2 (MBD2): TRFRET-based...
来源:The Scripps Research Institute Molecular Screening Center
靶标:E3 ubiquitin-protein ligase UHRF1 isoform 1 [Homo sapiens]
External Id:UHRF1-CPGDNA_INH_TRFRET_1536_1X%INH CSRUN for MBD2-CPGDNA INH
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实验名称:Luminescence-based cell-based primary high throughput screening assay for inhibitors ...
来源:The Scripps Research Institute Molecular Screening Center
靶标:nuclear receptor subfamily 0 group B member 1 [Homo sapiens]
External Id:DAX1-FULL_INH_LUMI_1536_1X%INH PRUN
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实验名称:uHTS identification of small molecule modulators of Rev-erb Alpha.
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1016-RevErbaLBD-Primary-Assay
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实验名称:HTS for Bacterial rRNA inhibitors Measured in Microorganism-Based System Using Plate ...
来源:Broad Institute
靶标:N/A
External Id:7056-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Fluorescence-based biochemical high throughput primary assay to identify inhibitors o...
来源:The Scripps Research Institute Molecular Screening Center
靶标:Phospholipase C, beta 3 (phosphatidylinositol-specific) [Homo sapiens]
External Id:PLCB3_INH_QFRET_1536_1X%INH 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:ADAM10 [Homo sapiens]
External Id:ADAM10_INH_QFRET_1536_1X%INH PRUN
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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:Protein DAF-12, isoform a [Caenorhabditis elegans]
External Id:HGDAF12_AG_LUMI_1536_1X%ACT PRUN
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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:Epi Absorbance-based biochemical primary high throughput screening assay to identify ...
来源:The Scripps Research Institute Molecular Screening Center
靶标:tyrosyl-DNA phosphodiesterase 2 [Homo sapiens]
External Id:TPD2_INH_EPIABS_1536_1X%INH PRUN
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| 2-methylsulfanyl-6H-thiazolo[5,4-d]pyrimidin-7-one |
| 2-(methylthio)-6,7-dihydropyrimido[5,4-d][1,3]thiazol-7-one |
| 2-Methylmercaptothiazolo<5,4-d>-pyrimidin-7(6H)-on |
| 2-methylsulfanylthiazolo[5,4-d]pyrimidine-7(6H)-one |
| 2-Methylmercapto-6H-thiazolo[5,4-d]pyrimidin-7-on |