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Hesperidin methylchalcone {[allProObj[0].p_purity_real_show]}

货号:A549207

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。

Hesperidin methylchalcone 化学结构 CAS号:24292-52-2
Hesperidin methylchalcone 化学结构
CAS号:24292-52-2
Hesperidin methylchalcone 3D分子结构
CAS号:24292-52-2
Hesperidin methylchalcone 化学结构 CAS号:24292-52-2
Hesperidin methylchalcone 3D分子结构 CAS号:24292-52-2
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Hesperidin methylchalcone 纯度/质量文件 产品仅供科研

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Hesperidin methylchalcone 生物活性

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].

Hesperidin methylchalcone 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice TiO2-induced chronic arthritis model Intraperitoneal injection 100 mg/kg Once daily for 30 days HMC inhibited mechanical hyperalgesia, thermal hyperalgesia, joint edema, leukocyte recruitment, and oxidative stress in the knee joint (alterations in gp91phox, GSH, superoxide anion, and lipid peroxidation) and in recruited leukocytes (total reactive oxygen species and GSH); reduced patellar proteoglycan degradation; and decreased pro-inflammatory cytokine production. HMC also reduced the activation of nociceptor-sensory TRPV1+ and TRPA1+ neurons. These effects occurred without renal, hepatic, or gastric damage. Molecules. 2023 Jan 15;28(2):872
Swiss mice Diclofenac-induced acute kidney injury Intra-peritoneal injection 0.03–3 mg/kg Single dose, evaluated after 24 hours To evaluate the protective effects of HMC on diclofenac-induced acute kidney injury. Results showed that HMC dose-dependently improved renal function markers (urea and creatinine levels), reduced oxidative stress and inflammatory responses. Antioxidants (Basel). 2022 Jun 27;11(7):1261

Hesperidin methylchalcone 参考文献

[1]Bussmann AJC,et al. The Flavonoid Hesperidin Methyl Chalcone Targets Cytokines and Oxidative Stress to Reduce Diclofenac-Induced Acute Renal Injury: Contribution of the Nrf2 Redox-Sensitive Pathway. Antioxidants (Basel). 2022 Jun 27;11(7):1261.

[2]Ruiz-Miyazawa KW, et al. Hesperidin Methylchalcone Suppresses Experimental Gout Arthritis in Mice by Inhibiting NF-κB Activation. J Agric Food Chem. 2018 Jun 27;66(25):6269-6280.

Hesperidin methylchalcone 实验方案

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

Hesperidin methylchalcone 技术信息

CAS号24292-52-2
分子式C29H36O15
分子量 624.59
SMILES Code OC1=CC(O[C@@H]([C@H](O)[C@H]2O)O[C@@H]([C@H]2O)CO[C@H]3[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O3)=CC(OC)=C1C(/C=C/C4=CC(O)=C(OC)C=C4)=O
MDL No. MFCD00010438
别名
运输蓝冰
InChI Key FDHNLHLOJLLXDH-JIYHLSBYSA-N
Pubchem ID 6436550
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: 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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
方案 二
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