 
        
        
        
                货号:A456389
                
                同义名:
                    
                        
                            
                                (+)-Anwulignan; Anwuligan
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Anwuligan 是从五味子(Schisandra chinensis)果实中分离和纯化的天然产物,具有对抗氧化应激和神经炎症的神经退行性疾病的治疗潜力。
 
                                 
                                
                            

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| 产品名称 | COX ↓ ↑ | COX-1 ↓ ↑ | COX-2 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Piroxicam | ✔ | 98% | |||||||||||||||||
| Salicylic acid | ✔ | 98% | |||||||||||||||||
| Phenacetin | ✔ | 98% | |||||||||||||||||
| Etodolac | ✔ | 99% | |||||||||||||||||
| Flunixin meglumine | ✔ | 98% | |||||||||||||||||
| Ibuprofen L-lysine | ✔ | 98% | |||||||||||||||||
| Nabumetone | ✔ | 98% | |||||||||||||||||
| Acemetacin | ✔ | 98% | |||||||||||||||||
| Diflunisal | ✔ | 98% | |||||||||||||||||
| Pranoprofen | ✔ | 98% | |||||||||||||||||
| Ampiroxicam | ✔ | 98% | |||||||||||||||||
| Meloxicam | ✔ | 98% | |||||||||||||||||
| Sulindac | ✔ | 98% | |||||||||||||||||
| Ketoprofen | ✔ | 98% | |||||||||||||||||
| Mefenamic Acid | ✔ | 95% | |||||||||||||||||
| Bromfenac sodium | ✔ | 98% | |||||||||||||||||
| Oxaprozin | ✔ | 99% | |||||||||||||||||
| Aspirin | ✔ | 99% | |||||||||||||||||
| Nepafenac | ✔ | 98% | |||||||||||||||||
| Zaltoprofen | ✔ | 99% | |||||||||||||||||
| Salicin | ✔ | 98% | |||||||||||||||||
| Suprofen | ✔ | 99%+ | |||||||||||||||||
| Xanthohumol | ✔ | 99% | |||||||||||||||||
| Parecoxib | ✔ | 98% | |||||||||||||||||
| Tolfenamic Acid | +++ COX-2, IC50: 0.2 μM | 98% | |||||||||||||||||
| Etoricoxib | ✔ | 99% | |||||||||||||||||
| Niflumic Acid | ✔ | 98% | |||||||||||||||||
| Valdecoxib | ++++ COX-2, IC50: 5 nM | 99+% | |||||||||||||||||
| Ibuprofen | + COX-1, IC50: 13 μM | + COX-2, IC50: 370 μM | 98% | ||||||||||||||||
| Indomethacin | ++ COX1, IC50: 0.28 μM | + COX-2, IC50: 14 μM | 97% | ||||||||||||||||
| Lornoxicam | ++++ COX-1, IC50: 5 nM | ++++ COX-2, IC50: 8 nM | 98% | ||||||||||||||||
| Meclofenamic acid sodium | ++++ COX-1, IC50: 40 nM | +++ COX-2, IC50: 50 nM | 99% | ||||||||||||||||
| Asaraldehyde | ✔ | 98% | |||||||||||||||||
| Naproxen | + COX-1, IC50: 8.7 μM | + COX-2, IC50: 5.2 μM | 98% | ||||||||||||||||
| Diclofenac Sodium Salt | +++ COX-1, IC50: 60 nM | +++ COX-2, IC50: 200 nM | 98% | ||||||||||||||||
| NS-398 | ++ COX-2, IC50: 3.8 μM | 95% | |||||||||||||||||
| Amfenac Sodium Hydrate | ++ COX-1, IC50: 250 nM | +++ COX-2, IC50: 150 nM | 98%+ | ||||||||||||||||
| Nimesulide | + COX-2, IC50: 26 μM | 98% | |||||||||||||||||
| Lumiracoxib | ++ COX-1, Ki: 3 μM | +++ COX-2, Ki: 60 nM | 98% | ||||||||||||||||
| Rutaecarpine | ✔ | 95% | |||||||||||||||||
| Celecoxib | ++++ COX-2, IC50: 40 nM | 98% | |||||||||||||||||
| Carprofen | ++++ canine COX2, IC50: 30 nM | 98% | |||||||||||||||||
| Ketorolac | ++ COX-1 (human), IC50: 1.23 μM | ++ COX-2 (human), IC50: 3.50 μM | 98% | ||||||||||||||||
| 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 | Anwuligan, a natural product isolated and purified from the fruits of Schisandra chinensis, possesses therapeutic potentials against neurodegenerative diseases with oxidative stress and neuroinflammation. | 
| Concentration | Treated Time | Description | References | |
| 3×Transgene-AD mouse primary neuron cells | 20 µM | 24 hours | To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 404 site | Front Nutr. 2022 May 18;9:892558 | 
| N2a/SweAPP cells | 0, 5, 10, 15, 20 µM | 24 hours | To investigate the effect of Macelignan on Aβ aggregation, results showed that Macelignan significantly reduced the expression levels of APP and Aβ | Front Nutr. 2022 May 18;9:892558 | 
| HEK293/Tau cells | 0, 5, 10, 15, 20 µM | 24 hours | To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 396, Ser 404, and Thr 231 sites | Front Nutr. 2022 May 18;9:892558 | 
| SH-SY5Y/Tau cells | 0, 5, 10, 15, 20 µM | 24 hours | To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 396, Ser 404, and Thr 231 sites | Front Nutr. 2022 May 18;9:892558 | 
| MCF-7 cells | 100 µM | 144 hours | To evaluate the effect of Macelignan on the proliferation of MCF-7 cells, results showed that 100 µM Macelignan increased cell proliferation to 201.07 ± 3.68% | Pharmaceutics. 2021 Jul 15;13(7):1082 | 
| H9c2 cardiomyoblast cells | 50 μM | 22 hours | To evaluate the protective effect of Macelignan against H2O2-induced oxidative stress, results showed that Macelignan significantly improved cell viability and reduced apoptosis | Sci Rep. 2021 Jan 12;11(1):664 | 
| HepG2 cells | 0–3 mM | 48h | Assess the cytotoxicity of Macelignan on HepG2 cells, showing low cytotoxicity. | Braz J Med Biol Res. 2016 Jul 4;49(7):e5313 | 
| Ascosphaera apis | 1.56 mg/mL (24h), 3.125 mg/mL (48h) | 24h, 48h | Evaluate the antifungal activity of Macelignan against Ascosphaera apis, showing significant growth inhibition. | Braz J Med Biol Res. 2016 Jul 4;49(7):e5313 | 
| Streptococcus sanguinis | 200 µg/ml | 24 hours | To evaluate the growth inhibitory effect of Macelignan on Streptococcus sanguinis, showing an inhibition zone diameter of 12.2±1.13 mm. | Oral Health Prev Dent. 2020 Jul 4;18(3):537-542 | 
| Streptococcus mutans | 200 µg/ml | 24 hours | To evaluate the growth inhibitory effect of Macelignan on Streptococcus mutans, showing an inhibition zone diameter of 11.8±0.67 mm. | Oral Health Prev Dent. 2020 Jul 4;18(3):537-542 | 
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | Chronic unpredictable mild stress (CUMS) model | Intragastric administration | 5 mg/kg | Daily administration for 30 days | Macelignan significantly improved CUMS-induced depression-like behaviors, including reduced immobility time in forced swimming and tail suspension tests. Additionally, Macelignan restored oxidative balance, suppressed neuroinflammation, and enhanced synaptic plasticity. | Transl Psychiatry. 2025 May 9;15(1):163 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 3.05mL 0.61mL 0.30mL | 15.23mL 3.05mL 1.52mL | 30.45mL 6.09mL 3.05mL | |
| CAS号 | 107534-93-0 | 
| 分子式 | C20H24O4 | 
| 分子量 | 328.4 | 
| SMILES Code | OC1=CC=C(C[C@H](C)[C@H](C)CC2=CC=C(OCO3)C3=C2)C=C1OC | 
| MDL No. | MFCD09953803 | 
| 别名 | (+)-Anwulignan; Anwuligan | 
| 运输 | 蓝冰 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C | 
| 溶解方案 | DMSO: 105 mg/mL(319.73 mM),配合低频超声助溶,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 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
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