货号:A166479
同义名:
柚皮芸香苷
/ Naringenin-7-O-rutinoside; Isonaringin
Narirutin是一种黄酮-7-O-糖苷,具有抗增殖、抗抑郁和抗炎作用。它可以从文旦(Citrus grandis (L.) Osbeck)的幼果中提取。


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| 描述 | Narirutin is a flavanone-7-O-glycoside with antiproliferative, anti-depressant and anti-inflammatory properties. It can be isolated from the young fruit of Citrus grandis (L.) Osbeck. It is considered to be non-toxic with predicted high LD50 value, 12000 mg/kg body weight. The phytochemical is tested for its antitubercular activity in vitro. It has MIC99 62.5 μg/mL against the MtbH37Rv strain[3]. At 10 mg/kg, but not 0.1 or 1 mg/kg, narirutin significantly diminished OVA-induced airway inflammation caused by infiltration of lung tissue with inflammatory and mucus-producing cells, as well as reduced eosinophil counts in the peripheral blood and bronchoalveolar lavage fluid (BALF), interleukin (IL)-4 levels in BALF and IgE levels in serum[4]. The inhibitory mechanism of narirutin on RBL-2H3 cells degranulation could be related to regulate MAPK, NF-κB and Tyrosine kinase signaling pathway[5]. NR (Narirutin) treatment for 1 week significantly alleviated the depressive-like behaviours of CMS-exposed mice, as indicated by restored decreased sucrose preference and shortened floating time in the forced swimming test. Moreover, NR treatment significantly blocked the CMS-induced anxiety-like behaviors, including increased time spent in the central zone in the open field test, and shortened the latency to feeding in the novelty suppressed feeding test[6]. Narirutin has vasorelaxing effect and the mechanism involves the inhibition of phosphodiesterase, which increases intracellular cAMP, thereby stimulating the endothelial nitric oxide synthase and activating the voltage-gated potassium channels in vascular smooth muscle cells[7]. |
| Concentration | Treated Time | Description | References | |
| HepG2 cells | 80 µM | 7 hours | To investigate the effect of NR on TFEB nuclear translocation, results showed NR promoted TFEB dephosphorylation and nuclear translocation via the PPP3/calcineurin pathway. | Autophagy. 2023 Aug;19(8):2240-2256 |
| Mouse primary hepatocytes | 80 µM | 8 hours | To evaluate the protective effects of NR on APAP-induced cell damage, results showed NR enhanced cell viability, decreased activities of GPT and GOT1, and improved mitochondrial dysfunction. | Autophagy. 2023 Aug;19(8):2240-2256 |
| Human embryonic kidney (HEK) 293 cell line | 20 µM | Overnight | Blocks voltage-gated sodium (Na V) channels subtype 1.7 | Int J Mol Sci. 2022 Nov 27;23(23):14842 |
| Rat dorsal root ganglion (DRG) neurons | 20 µM | Overnight | Inhibits Veratridine-triggered nociceptor activities | Int J Mol Sci. 2022 Nov 27;23(23):14842 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | LPS-induced acute lung injury model | Intraperitoneal injection | 20 mg/kg and 40 mg/kg | Once daily for seven days | Narirutin pretreatment alleviates LPS-induced acute lung injury by regulating TLR4/NF-κB mediated inflammation | J Inflamm Res. 2024 Oct 21;17:7503-7520 |
| Adult male rats | Spared nerve injury (SNI)-induced neuropathic pain model | Intrathecal injection | 20 μg/20 μL | Single administration, effects lasted for about 3 hours | Alleviates mechanical allodynia and cold allodynia | Int J Mol Sci. 2022 Nov 27;23(23):14842 |
| Rats | Depression-like behavior model induced by high sugar diet (HSD) and cafeteria diet | Dietary supplementation | 30 mg/kg | Continuous supplementation during pregnancy and lactation | To evaluate the preventive effect of Narirutin on depression-like behavior induced by maternal high sugar diet and cafeteria diet. Results showed that Narirutin supplementation reversed the depression-like behavior induced by cafeteria diet. | Nutrients. 2019 Mar 7;11(3):572 |
| BALB/c mice | OVA-induced food allergy model | Intragastric administration | 30 mg/kg and 50 mg/kg | Tolerance establishment stage (D0–D4), sensitization stage (D11–D18), and excitation phase (D25–D39) | To investigate the protective effects of Narirutin on OVA-induced food allergy, results showed that Narirutin may exert protective effects by increasing Lachnospiraceae abundance | Nutrients. 2025 May 8;17(10):1611 |
| C57BL/6J mice | APAP-induced liver injury model | Intraperitoneal injection | 50 mg/kg | Administered 1 hour after APAP injection, lasting for 5 or 23 hours | To evaluate the protective effects of NR on APAP-induced liver injury and oxidative stress, results showed NR reduced liver necrosis, decreased serum GPT and GOT1 activities, elevated antioxidant enzyme activities, and improved mitochondrial function. | Autophagy. 2023 Aug;19(8):2240-2256 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
1.72mL 0.34mL 0.17mL |
8.61mL 1.72mL 0.86mL |
17.23mL 3.45mL 1.72mL |
|
| CAS号 | 14259-46-2 |
| 分子式 | C27H32O14 |
| 分子量 | 580.53 |
| SMILES Code | O=C1C[C@@H](C2=CC=C(O)C=C2)OC3=C1C(O)=CC(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)O4)=C3 |
| MDL No. | MFCD00017316 |
| 别名 | 柚皮芸香苷 ;Naringenin-7-O-rutinoside; Isonaringin; Narirutin, Isonaringenin, Isonaringin, Naringenin 7-beta-rutinoside, Naringenin 7-O-rutinoside, (2S)-Narirutin; (2S)-Narirutin |
| 运输 | 蓝冰 |
| InChI Key | HXTFHSYLYXVTHC-AJHDJQPGSA-N |
| Pubchem ID | 442431 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, room temperature |
| 溶解方案 |
DMSO: 120 mg/mL(206.71 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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