3-(4-吡啶)吲哚结构式
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常用名 | 3-(4-吡啶)吲哚 | 英文名 | Rho Kinase Inhibitor III,Rockout |
|---|---|---|---|---|
| CAS号 | 7272-84-6 | 分子量 | 194.23200 | |
| 密度 | 1.211g/cm3 | 沸点 | 406.7ºC at 760 mmHg | |
| 分子式 | C13H10N2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 185.2ºC |
3-(4-吡啶)吲哚用途3-(4-吡啶基)吲哚(Rockout)是一种Rho激酶(ROCK)抑制剂,IC50为25μM。在伤口愈合试验中,3-(4-吡啶基)吲哚可抑制起泡并导致肌动蛋白应力纤维溶解【1】。 |
| 中文名 | 3-(4-吡啶)吲哚 |
|---|---|
| 英文名 | 3-pyridin-4-yl-1H-indole |
| 英文别名 | 更多 |
| 描述 | 3-(4-吡啶基)吲哚(Rockout)是一种Rho激酶(ROCK)抑制剂,IC50为25μM。在伤口愈合试验中,3-(4-吡啶基)吲哚可抑制起泡并导致肌动蛋白应力纤维溶解【1】。 |
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| 相关类别 | |
| 参考文献 |
| 密度 | 1.211g/cm3 |
|---|---|
| 沸点 | 406.7ºC at 760 mmHg |
| 分子式 | C13H10N2 |
| 分子量 | 194.23200 |
| 闪点 | 185.2ºC |
| 精确质量 | 194.08400 |
| PSA | 28.68000 |
| LogP | 3.22990 |
| InChIKey | LLJRXVHJOJRCSM-UHFFFAOYSA-N |
| SMILES | c1ccc2c(-c3ccncc3)c[nH]c2c1 |
| 折射率 | 1.688 |
| 储存条件 | -20°C |
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~60%
3-(4-吡啶)吲哚 7272-84-6 |
| 文献:Chahma; Combellas; Thiebault Synthesis, 1994 , # 4 p. 366 - 368 |
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~30%
3-(4-吡啶)吲哚 7272-84-6 |
| 文献:Beevers, Rebekah E.; Buckley, George M.; Davies, Natasha; Fraser, Joanne L.; Galvin, Francis C.; Hannah, Duncan R.; Haughan, Alan F.; Jenkins, Kerry; Mack, Stephen R.; Pitt, William R.; Ratcliffe, Andrew J.; Richard, Marianna D.; Sabin, Verity; Sharpe, Andrew; Williams, Sophie C. Bioorganic and Medicinal Chemistry Letters, 2006 , vol. 16, # 9 p. 2535 - 2538 |
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~69%
3-(4-吡啶)吲哚 7272-84-6 |
| 文献:Lamar, Angus A.; Nicholas, Kenneth M. Tetrahedron, 2009 , vol. 65, # 19 p. 3829 - 3833 |
| 3-(4-吡啶)吲哚上游产品 5 | |
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| 3-(4-吡啶)吲哚下游产品 0 | |
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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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
来源:Burnham Center for Chemical Genomics
靶标:cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id:SBCCG-A764-CF-PAF-Primary-Assay
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ant...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_ANT_FLUO8_1536_1X%INH PRUN
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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:Trypanosoma brucei RNA editing ligase 1
External Id:TBREL1_INH_FRET_1536_1X%INH PRUN
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify act...
来源:The Scripps Research Institute Molecular Screening Center
靶标:TTR [Homo sapiens]
External Id:TTR_ACT_LUMI_1536_1X%ACT PRUN
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实验名称:Millipore: Percentage of residual kinase activity of PRKAA2 at 10uM relative to contr...
来源:ChEMBL
靶标:5'-AMP-activated protein kinase catalytic subunit alpha-1
External Id:CHEMBL2219380
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实验名称:Millipore: Percentage of residual kinase activity of NUAK1 at 1uM relative to control...
来源:ChEMBL
靶标:NUAK family SNF1-like kinase 1
External Id:CHEMBL2219381
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| rockout |
| 3-(4-Pyridyl)-1H-indole |
| 3-<Pyridyl-(4)>-indol |
| 3-(pyridin-4-yl)-1H-indole |
| 3-(PYRIDIN-4-YL)INDOLE |
| 3-(4-Pyridyl)indole |
| 4-(3-indolyl)-pyridine |