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                同义名:
                    
                        
                            
                                Flagecidin; Wuningmeisu C
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Anisomycin是一种天然抗生素,既能作为应激活化蛋白激酶(JNK/SAPK 和 p38 MAPK)的强效激活剂,也能通过阻断翻译抑制蛋白质合成。
 
                                 
                                
                            

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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 | ✔ | ERK,STAT | 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。 | |||||||||||||||||||
| 描述 | c-Jun N-terminal kinase (JNK) is a member of the mitogen-activated protein kinases (MAPK) family. Anisomycin is an activator of both JNK and p38[3]. The incubation of HL-1 myocytes with 50ng/mL anisomycin for 24 h markedly increased the protein level of CaMKIIδ by ∼60% relative to the control group. The c-jun phosphorylation in total cell lysates and nuclear extracts was also increased by the treatment of 50ng/mL HL-1 myocytes with anisomycin for 24 h[4]. The intraperitoneal injection of wild-type, TNFR p55/p75-/-, and Nox2-/- mice with 0.1mg/kg anisomycin resulted in the activation of p38, an increase in the production of TNF-α and Nox2, and the phosphorylation of Nox2 compared with the control group[5]. | 
| Concentration | Treated Time | Description | References | |
| HeLa cells | 50μM | 20 minutes | To investigate the role of p38 in EphA2 Ser-897 phosphorylation, results showed anisomycin induced EphA2 phosphorylation via the p38 pathway. | J Biol Chem. 2023 May;299(5):104699 | 
| AML12 cells | 10 μM | 2 h | Activated JNK signaling pathway, increased TG accumulation, and partially deprived the therapeutic role of Tamoxifen | Signal Transduct Target Ther. 2023 Mar 3;8(1):94. | 
| Cell monolayers derived from pig jejunum organoids | 1 µM | 24 h | Anisomycin disrupted the epithelial barrier integrity but failed to induce a significant increase in paracellular permeability. Butyrate (BUT) prevented the disruption of epithelial barrier integrity induced by ANI. | Gut Microbes. 2024 Jan-Dec;16(1):2430424. | 
| SK-MES-1 | 0.5 µM | 24 h | Anisomycin pre-treatment activated p38 and HSP27 and induced apoptosis. | Int J Biol Sci. 2020 Sep 2;16(15):2883-2894. | 
| NCI-H520 | 0.5 µM | 24 h | Anisomycin pre-treatment activated p38 and HSP27 and induced apoptosis. | Int J Biol Sci. 2020 Sep 2;16(15):2883-2894. | 
| murine neonatal cardiomyocytes | 25 ng/mL | 1 hour | Pretreatment with anisomycin partially abolished the protective effects of NG-R1 against H/R-induced cardiomyocyte apoptosis. | Acta Pharmacol Sin. 2023 Jul;44(7):1366-1379. | 
| Administration | Dosage | Frequency | Description | References | ||
| Mice | MCD diet-induced NASH model | Intraperitoneal injection | 50 mg/kg | 5 consecutive days | Activated JNK signaling pathway and partially abolished the therapeutic effect of Tamoxifen on hepatic steatosis | Signal Transduct Target Ther. 2023 Mar 3;8(1):94. | 
| Rats | Fear memory model | Bilateral infusion into the basolateral amygdala | 125 mg/ml | Single administration | To evaluate the effect of Anisomycin on fear memory reconsolidation blockade, results showed that Anisomycin effectively blocked memory reconsolidation in rats trained with 1P, but had no effect in rats trained with 10P. | Elife. 2020 May 18;9:e57010 | 
| Mice | Depressive-like behavior model | Intraperitoneal injection | 100 mg/kg | Single injection, behavioral tests performed 3 hours later | To evaluate the effect of Anisomycin on depressive-like behavior in mice, results showed that Anisomycin increased immobility time in TST and latency to feed in NSF. | Transl Psychiatry. 2024 Oct 1;14(1):397 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 3.77mL 0.75mL 0.38mL | 18.85mL 3.77mL 1.88mL | 37.69mL 7.54mL 3.77mL | |
| CAS号 | 22862-76-6 | 
| 分子式 | C14H19NO4 | 
| 分子量 | 265.31 | 
| SMILES Code | O[C@@H]1[C@@H](OC(C)=O)[C@@H](CC2=CC=C(OC)C=C2)NC1 | 
| MDL No. | MFCD00077650 | 
| 别名 | Flagecidin; Wuningmeisu C; AI3-50846; NSC 76712 | 
| 运输 | 蓝冰 | 
| InChI Key | YKJYKKNCCRKFSL-RDBSUJKOSA-N | 
| Pubchem ID | 253602 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, store in freezer, under -20°C | 
| 溶解方案 | DMSO: 50 mg/mL(188.46 mM),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 H2O: 4 mg/mL(15.08 mM),配合低频超声,并水浴加热至45℃助溶 
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