3-(甲基磺酰胺基)苯甲酸甲酯结构式
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常用名 | 3-(甲基磺酰胺基)苯甲酸甲酯 | 英文名 | Methyl 3-(methylsulfonamido)benzoate |
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| CAS号 | 32087-05-1 | 分子量 | 229.25300 | |
| 密度 | 1.366g/cm3 | 沸点 | 362ºC at 760 mmHg | |
| 分子式 | C9H11NO4S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 172.7ºC |
| 中文名 | 3-(甲基磺酰胺基)苯甲酸甲酯 |
|---|---|
| 英文名 | Methyl 3-[(methylsulfonyl)amino]benzoate |
| 英文别名 | 更多 |
| 密度 | 1.366g/cm3 |
|---|---|
| 沸点 | 362ºC at 760 mmHg |
| 分子式 | C9H11NO4S |
| 分子量 | 229.25300 |
| 闪点 | 172.7ºC |
| 精确质量 | 229.04100 |
| PSA | 80.85000 |
| LogP | 1.99850 |
| InChIKey | UQIOKJVVJMHUTP-UHFFFAOYSA-N |
| SMILES | COC(=O)c1cccc(NS(C)(=O)=O)c1 |
| 外观性状 | 白色粉末 |
| 折射率 | 1.568 |
| 储存条件 | 密封,干燥,室温 |
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~58%
3-(甲基磺酰胺基)苯甲酸甲酯 32087-05-1 |
| 文献:SIGNAL PHARMACEUTICALS, LLC Patent: WO2008/51494 A1, 2008 ; Location in patent: Page/Page column 119 ; |
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~96%
3-(甲基磺酰胺基)苯甲酸甲酯 32087-05-1 |
| 文献:Deng, Wei; Liu, Lei; Zhang, Chen; Liu, Min; Guo, Qing-Xiang Tetrahedron Letters, 2005 , vol. 46, # 43 p. 7295 - 7298 |
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~%
3-(甲基磺酰胺基)苯甲酸甲酯 32087-05-1 |
| 文献:Rahaim Jr., Ronald J.; Maleczka Jr., Robert E. Synthesis, 2006 , # 19 p. 3316 - 3340 |
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~%
3-(甲基磺酰胺基)苯甲酸甲酯 32087-05-1 |
| 文献:Wells; Strahl Journal of pharmaceutical sciences, 1971 , vol. 60, # 4 p. 533 - 536 |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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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: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: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: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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