Hesperidin methylchalcone是一种来源于柑橘的化合物,具有强效的抗氧化和抗炎活性。它通过抑制氧化应激、细胞因子产生和 NF-κB 活化来减少炎症和疼痛,同时具有血管保护作用。Hesperidin methylchalcone 在心血管疾病、炎症性疾病和抗氧化保健品领域中具有潜在应用价值。
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描述 | Hesperidin methylchalcone, an orally active flavonoid, possesses analgesic, anti-inflammatory, and antioxidant effects. It demonstrates vasoprotective activity and inhibits oxidative stress, cytokine production, and NF-κB activation. Hesperidin methylchalcone is applicable in gout disease research[1][2]. |
体内研究 | Hesperidin methylchalcone (0.03-3 mg/kg, i.p., once time) dose-dependently reduces the increase of renal dysfunction markers (urea and creatinine) caused by SDCF in mice[1]. Hesperidin methylchalcone (3 mg/kg, i.p., once time) effectively mitigates oxidative stress induced by SDCF in the renal tissue of mice[1]. Hesperidin methylchalcone (3 mg/kg, i.p., single dose) alleviates SDCF-induced renal histopathology, swelling, and cytotoxicity in tubular cells of mice[1]. Hesperidin methylchalcone (3-30 mg/kg, p.o., single dose) dose-dependently diminishes MSU-induced hyperalgesia, edema, and leukocyte infiltration in mice[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.60mL 0.32mL 0.16mL |
8.01mL 1.60mL 0.80mL |
16.01mL 3.20mL 1.60mL |
CAS号 | 24292-52-2 |
分子式 | C29H36O15 |
分子量 | 624.587 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 50 mg/mL(80.05 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 |
动物实验配方 |