 
        
        
        
                货号:A891284
                
                同义名:
                    
                        
                            蓄苷
                            
                             / Quercetin 3-O-α-L-arabinofuranoside
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Avicularin是一种黄酮类化合物,通过抑制 NF-κB、COX-2 和 PPAR-γ 表现出抗炎、抗肿瘤和保肝作用,可用于免疫调节及代谢性疾病的研究。
 
                                 
                                
                            

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| 产品名称 | ERK ↓ ↑ | ERK1 ↓ ↑ | ERK2 ↓ ↑ | ERK5 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| DEL-22379 | + ERK, IC50: 0.5 μM | + ERK, IC50: 0.5 μM | 98% | ||||||||||||||||
| Pluripotin | ++ ERK1, Kd: 98 nM | RasGAP | 98+% | ||||||||||||||||
| FR 180204 | + ERK1, Ki: 0.31 μM | ++ ERK2, Ki: 0.14 μM | 98% | ||||||||||||||||
| Ravoxertinib | +++ ERK1, IC50: 1.1 nM | ++++ ERK2, IC50: 0.3 nM | 99%+ | ||||||||||||||||
| SCH772984 | +++ ERK1, IC50: 4 nM | ++++ ERK2, IC50: 1 nM | 99%+ | ||||||||||||||||
| Temuterkib | +++ ERK1, IC50: 5 nM | +++ ERK2, IC50: 5 nM | 99%+ | ||||||||||||||||
| VX-11e | +++ ERK2, Ki: <2 nM | 99%+ | |||||||||||||||||
| Ulixertinib | ++++ ERK2, IC50: <0.3 nM | 99%+ | |||||||||||||||||
| XMD17-109 | ++ ERK5, IC50: 162 nM | 99%+ | |||||||||||||||||
| 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。 | |||||||||||||||||||
| 产品名称 | PPARα ↓ ↑ | PPARβ/δ ↓ ↑ | PPARγ ↓ ↑ | PPARδ ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Fenofibric acid | ✔ | 98% | |||||||||||||||||
| GW6471 | ++ PPARα, IC50: 0.24 μM | 99%+ | |||||||||||||||||
| GSK3787 | ++ PPARδ, pIC50: 6.6 | ++ PPARδ, pIC50: 6.6 | 99%+ | ||||||||||||||||
| FH535 | ✔ | 98%+ | |||||||||||||||||
| GW9662 | +++ PPARα, IC50: 32 nM | +++ PPARγ, IC50: 3.3 nM | 98% | ||||||||||||||||
| T0070907 | ++++ PPARγ, IC50: 1 nM | 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。 | |||||||||||||||||||
| 产品名称 | GLUT1 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| STF-31 | ✔ | 99%+ | |||||||||||||||||
| BAY-876 | +++ GLUT1, IC50: 0.002 μM | 99%+ | |||||||||||||||||
| WZB117 | ++ GLUT1, IC50: 10μM | 99+% | |||||||||||||||||
| 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。 | |||||||||||||||||||
| 产品名称 | NF-κB ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ammonium pyrrolidine-1-carbodithioate | ✔ | 98% | |||||||||||||||||
| QNZ | ++++ NF-κB, IC50: 11 nM | 99%+ | |||||||||||||||||
| Sodium 4-Aminosalicylate Dihydrate | ✔ | 98% | |||||||||||||||||
| Sodium Salicylate | ✔ | 95% | |||||||||||||||||
| Parthenolide | ✔ | p53 | 97% HPLC | ||||||||||||||||
| JSH-23 | + NF-κB, IC50: 7.1 μM | 98% | |||||||||||||||||
| Phenethyl caffeate | ✔ | 98% | |||||||||||||||||
| Andrographolide | ✔ | 98+% | |||||||||||||||||
| Curcumin | ✔ | Nrf2,HDAC | 98% | ||||||||||||||||
| SC75741 | +++ NF-κB, EC50: 200 nM | 99%+ | |||||||||||||||||
| CBL0137 HCl | ++ NF-κB, EC50: 0.47 μM | p53 | 99%+ | ||||||||||||||||
| 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。 | |||||||||||||||||||
| 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 | Avicularin, an orally active flavonoid, attenuates activities of NF-κB (p65), COX-2, and PPAR-γ, exhibiting anti-inflammatory, anti-infectious, anti-allergic, antioxidant, hepatoprotective, and anti-tumor properties[1][3]. | 
| 体外研究 | Avicularin, at concentrations of 10-300 μM and a one-hour exposure, diminishes NO and PGE2 production in LPS-stimulated RAW 264.7 cells[1]. | 
| Concentration | Treated Time | Description | References | |
| Huh7 cells | 100, 50, 25 µg/ml | 12, 24, 36, 48 hours | Avicularin significantly inhibited Huh7 cell proliferation in a concentration-dependent manner and suppressed cell migration and invasion. | Mol Med Rep. 2019 Jun;19(6):5417-5423. | 
| Α-glucosidase | 17.05 ± 0.75 μg/mL (IC50) | 15 minutes | To evaluate the inhibitory activity of Avicularin against α-glucosidase, results showed an IC50 value of 17.05 ± 0.75 μg/mL, indicating significant inhibitory effect. | Saudi Pharm J. 2023 Aug;31(8):101677. | 
| RAW264.7 macrophages | 0, 10, 30, 100, 300, 600 µM | 24 hours | To evaluate the effect of AL on the viability of RAW264.7 macrophages, results showed that AL at 10-300 μM did not significantly affect cell viability. | J Agric Food Chem. 2023 Jan 11;71(1):411-420. | 
| RAW 264.7 cells | 30, 100 and 300 µM | 24 hours | To investigate the inhibitory effect of AL on LPS-induced inflammatory response, results showed that AL significantly suppressed the expression of iNOS, COX-2, IL-6, TNF-α and IL-1β. | J Cell Mol Med. 2023 Nov;27(21):3326-3338. | 
| Bone marrow-derived macrophages (BMMs) | 0, 10, 30, 100, 300 µM | 5 days | To evaluate the effect of AL on the differentiation of BMMs into osteoclasts, results showed that AL significantly inhibited osteoclast formation and activity. | J Agric Food Chem. 2023 Jan 11;71(1):411-420. | 
| HepG2 cells | 10, 20 and 40 µM | 6 hours | To investigate the inhibitory effect of AL on D-GalN-induced ferroptosis, results showed that AL significantly reduced MDA, ROS and iron levels, increased GSH content, and upregulated the expression of GPX4 and xCT. | J Cell Mol Med. 2023 Nov;27(21):3326-3338. | 
| MDCK cells | 300 to 3.7 µg/mL | 72 hours | To evaluate the cytotoxicity of the extracts and determine their 50% cytotoxic concentration (CC50). | Foods. 2024 Dec 11;13(24):4008. | 
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | Ovariectomy (OVX)-induced osteoporosis model | Intraperitoneal injection | 1.25 mg/kg, 5 mg/kg | Every 2 days for 8 weeks | To evaluate the protective effect of AL on OVX-induced osteoporosis in mice, results showed that AL significantly increased bone mineral density and reduced the expression of bone resorption marker CTX-1. | J Agric Food Chem. 2023 Jan 11;71(1):411-420. | 
| ICR mice | Pb-induced nerve damage model | Intragastric administration | 25 mg/kg and 50 mg/kg | Once daily for 3 months | To evaluate the protective effects of AVL against Pb-induced neurotoxicity, results showed that AVL significantly ameliorated Pb-induced memory impairment, neuroinflammation, ferroptosis, and oxidative stress. | Antioxidants (Basel). 2024 Aug 22;13(8):1024 | 
| ICR mice | Lead-induced liver injury model | Intragastric administration | 25 mg/kg and 50 mg/kg | Once daily for 3 months | Evaluate the protective effects of Avi against Pb-induced hepatotoxicity, results showed that Avi significantly alleviated Pb-induced hepatic inflammation, endoplasmic reticulum stress (ERS), and glucose metabolism disorder | Nutrients. 2022 Nov 13;14(22):4806 | 
| Male C57BL/6 mice | LPS/D-GalN-induced acute liver failure model | Intragastric administration | 50 mg/kg | Once daily for 3 days | To investigate the protective effect of AL on LPS/D-GalN-induced acute liver failure, results showed that AL significantly alleviated hepatic pathological injury, reduced ALT and AST levels, and inhibited inflammatory response and ferroptosis. | J Cell Mol Med. 2023 Nov;27(21):3326-3338. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.30mL 0.46mL 0.23mL | 11.51mL 2.30mL 1.15mL | 23.02mL 4.60mL 2.30mL | |
| CAS号 | 572-30-5 | 
| 分子式 | C20H18O11 | 
| 分子量 | 434.35 | 
| SMILES Code | O=C1C(O[C@H]2[C@@H]([C@H]([C@H](CO)O2)O)O)=C(C3=CC=C(O)C(O)=C3)OC4=CC(O)=CC(O)=C14 | 
| MDL No. | MFCD10566630 | 
| 别名 | 蓄苷 ;Quercetin 3-O-α-L-arabinofuranoside | 
| 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(241.74 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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