trimethyl(3-oxobutyl)azanium,iodide结构式
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常用名 | trimethyl(3-oxobutyl)azanium,iodide | 英文名 | trimethyl(3-oxobutyl)azanium,iodide |
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| CAS号 | 31034-98-7 | 分子量 | 257.11300 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C7H16INO | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | trimethyl(3-oxobutyl)azanium,iodide |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C7H16INO |
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| 分子量 | 257.11300 |
| 精确质量 | 257.02800 |
| PSA | 17.07000 |
| InChIKey | GUIWMJZVPUIZPM-UHFFFAOYSA-M |
| SMILES | CC(=O)CC[N+](C)(C)C.[I-] |
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~%
trimethyl(3-oxo... 31034-98-7 |
| 文献:Kost; Erschow Zhurnal Obshchei Khimii, 1957 , vol. 27, p. 1722,1726; engl. Ausg. S. 1793, 1796 Full Text Show Details Ing et al. British Journal of Pharmacology and Chemotherapy, 1952 , vol. 7, p. 103,114 |
| trimethyl(3-oxobutyl)azanium,iodide上游产品 2 | |
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| trimethyl(3-oxobutyl)azanium,iodide下游产品 2 | |
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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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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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:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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| N-Butan-3-one-N,N,N-trimethylammonium iodide |
| AMMONIUM,N-BUTAN-3-ONE-N,N,N-TRIMETHYL-,IODIDE |
| 4-diethylamino-2-butanone |
| 1-diethylaminobutan-3-one methiodide |
| 3-Ketobutyltrimethylammonium iodide |