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                同义名:
                    
                        
                            
                                JNK Inhibitor II, negative control; 2-methyldibenzo[cd,g]indazol-6(2H)-one
                            
                        
                    
                
                
                
                    
                     
                
            
SP 600125, negative control是 SP 600125 的烷基衍生物,作为阴性对照用于研究。其不具显著的 JNK 抑制活性,因此用于确认 SP 600125 对 JNK(c-Jun N-terminal kinase)的特异性抑制效果。
 
                                 
                                
                            

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| 产品名称 | JNK ↓ ↑ | JNK1 ↓ ↑ | JNK2 ↓ ↑ | JNK3 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Mulberroside A | ✔ | 99%+ | |||||||||||||||||
| Loureirin B | ✔ | Calcium Channel,Potassium Channel | 99%+ | ||||||||||||||||
| Ginsenoside Re | ✔ | NF-κB | 98% | ||||||||||||||||
| (+)-(3R,8S)-Falcarindiol | ✔ | STAT,ERK | 99%+ | ||||||||||||||||
| trans-Zeatin | ✔ | ERK,p38 MAPK | 95+% | ||||||||||||||||
| Urolithin B | ✔ | ERK,NF-κB | 95% | ||||||||||||||||
| Cucurbitacin IIb | ✔ | NF-κB | 99% | ||||||||||||||||
| Astragaloside IV | ✔ | Akt,mTOR,NF-κB | 98% | ||||||||||||||||
| m-PEG25-NHS ester | ✔ | 95% | |||||||||||||||||
| NDMC101 | ✔ | 99%+ | |||||||||||||||||
| DB07268 | ++++ JNK1, IC50: 9 nM | 99%+ | |||||||||||||||||
| SP600125 | + MKK4, IC50: 0.4 μM | +++ JNK1, IC50: 40 nM | +++ JNK2, IC50: 40 nM | +++ JNK3, IC50: 90 nM | 98% | ||||||||||||||
| JNK-IN-7 | ++++ JNK1, IC50: 1.5 nM | ++++ JNK2, IC50: 2 nM | ++++ JNK3, IC50: 0.7 nM | 99% | |||||||||||||||
| JNK-IN-8 | ++++ JNK1, IC50: 4.7 nM | +++ JNK2, IC50: 18.7 nM | ++++ JNK3, IC50: 1 nM | 99%+ | |||||||||||||||
| 3,3',5-Triiodo-L-thyronine | ++ JNK1, Kd: 240 nM | ++ JNK2, Kd: 290 nM | +++ JNK3, Kd: 66 nM | 98% | |||||||||||||||
| IQ-1S free acid | + JNK1, IC50: 390 nM | ++ JNK2, IC50: 360 nM | +++ JNK3, IC50: 87 nM | 99% | |||||||||||||||
| BI-78D3 | ++ JNK, IC50: 280 nM | ++ JNK, IC50: 280 nM | ++ JNK, IC50: 280 nM | ++ JNK, IC50: 280 nM | 99%+ | ||||||||||||||
| Bentamapimod | +++ JNK1, IC50: 80 nM | +++ JNK2, IC50: 90 nM | ++ JNK3, IC50: 230 nM | 98% | |||||||||||||||
| Resveratrol | + JNK1, IC50: 50 μM | 98% | |||||||||||||||||
| Indirubin-3′-oxime | ✔ | 99%+ | |||||||||||||||||
| SU3327 | + JNK, IC50: 0.7 μM | + JNK, IC50: 0.7 μM | + JNK, IC50: 0.7 μM | + JNK, IC50: 0.7 μM | 99%+ | ||||||||||||||
| JNK Inhibitor VIII | ++++ JNK1, Ki: 2 nM JNK1, IC50: 45 nM | ++++ JNK2, IC50: 160 nM JNK2, Ki: 4 nM | +++ JNK3, Ki: 52 nM | 98% | |||||||||||||||
| Doramapimod | ✔ | 99%+ | |||||||||||||||||
| RPI-1 | ✔ | 99% | |||||||||||||||||
| TCS JNK 5a | ++ JNK2, pIC50: 6.5 | ++ JNK3, pIC50: 6.7 | 98% | ||||||||||||||||
| SP 600125, negative control | + JNK2, IC50: 18 μM | + JNK3, IC50: 24 μM | 97% | ||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 靶点 | 
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| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 4.27mL 0.85mL 0.43mL | 21.34mL 4.27mL 2.13mL | 42.69mL 8.54mL 4.27mL | |
| CAS号 | 54642-23-8 | 
| 分子式 | C15H10N2O | 
| 分子量 | 234.25 | 
| SMILES Code | O=C1C2=C3C(N(C)N=C3C4=CC=CC=C14)=CC=C2 | 
| MDL No. | MFCD00446029 | 
| 别名 | JNK Inhibitor II, negative control; 2-methyldibenzo[cd,g]indazol-6(2H)-one; N1-Methyl-1,9-pyrazoloanthrone; 54642-23-8; negative control; JNK inhibitor II | 
| 运输 | 蓝冰 | 
| InChI Key | ODZGYELAMAOARP-UHFFFAOYSA-N | 
| Pubchem ID | 11665831 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, store in freezer, under -20°C | 
| 溶解方案 | DMSO: 9 mg/mL(38.42 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO | 
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