2,4,6-三甲基-n-[2-(三氟甲基)苯基]苯磺酰胺结构式
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常用名 | 2,4,6-三甲基-n-[2-(三氟甲基)苯基]苯磺酰胺 | 英文名 | o-3M3FBS |
|---|---|---|---|---|
| CAS号 | 313981-55-4 | 分子量 | 343.36400 | |
| 密度 | 1.316g/cm3 | 沸点 | 424.3ºC at 760mmHg | |
| 分子式 | C16H16F3NO2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 210.4ºC |
用途o-3M3FBS是m-3M3FBS的阴性对照。o-3M3FBS通过独立于PLC的机制以对抗方式抑制内向和外向电流。相比之下,o-3M3FBS还以激动的方式导致[Ca2+]i增加[1]。 |
| 中文名 | 2,4,6-三甲基-n-[2-(三氟甲基)苯基]苯磺酰胺 |
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| 英文名 | 2,4,6-trimethyl-N-[2-(trifluoromethyl)phenyl]benzenesulfonamide |
| 英文别名 | 更多 |
| 描述 | o-3M3FBS是m-3M3FBS的阴性对照。o-3M3FBS通过独立于PLC的机制以对抗方式抑制内向和外向电流。相比之下,o-3M3FBS还以激动的方式导致[Ca2+]i增加[1]。 |
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| 相关类别 | |
| 体内研究 | o-3M3FBS(10μM)将AUC从对照组的1058±189 g/min(在存在TTX的情况下)降低至840±134 g/min。更高浓度的o-3M3FBS(25μM)将AUC进一步降低至457±59 g/min[1]。 |
| 参考文献 |
| 密度 | 1.316g/cm3 |
|---|---|
| 沸点 | 424.3ºC at 760mmHg |
| 分子式 | C16H16F3NO2S |
| 分子量 | 343.36400 |
| 闪点 | 210.4ºC |
| 精确质量 | 343.08500 |
| PSA | 54.55000 |
| LogP | 5.58520 |
| InChIKey | SKJJIFRWCCSXGL-UHFFFAOYSA-N |
| SMILES | Cc1cc(C)c(S(=O)(=O)Nc2ccccc2C(F)(F)F)c(C)c1 |
| 折射率 | 1.547 |
| 储存条件 | -20°C,密闭,干燥 |
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实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
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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:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
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实验名称:SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response f...
来源:ChEMBL
靶标:Replicase polyprotein 1ab
External Id:CHEMBL4495582
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实验名称:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
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实验名称:qHTS for inhibitors of Vif-A3G interactions: Validation
来源:NCGC
靶标:DNA dC->dU-editing enzyme APOBEC-3G [Homo sapiens]
External Id:VIFG001
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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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实验名称:Enzymatic assay of human HDAC6 with commercial peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808149
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实验名称:EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Rea...
来源:Broad Institute
靶标:histone-lysine N-methyltransferase EZH2 isoform a [Homo sapiens]
External Id:2125-01_Inhibitor_SinglePoint_HTS_Activity
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| HMS3268M14 |
| O-3M3FBS |
| Tocris-1942 |