Asperuloside 是一种环烯醚萜苷,来源于蛇舌草,具有抗炎活性。它通过抑制诱导型一氧化氮合酶 (iNOS)、NF-κB 和 MAPK 信号通路来发挥作用,可用于抗炎相关研究。
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产品名称 | eNOS ↓ ↑ | iNOS ↓ ↑ | nNOS ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1400W 2HCl |
+
eNOS, Ki: 50 μM |
++++
iNOS, Kd: <7 nM |
++
nNOS, Ki: 2 μM |
99%+ | |||||||||||||||
H-Arg(NO2)-OMe·HCl |
+++
eNOS, Ki: 39 nM |
++
iNOS, Ki: 4.4 μM |
+++
nNOS, Ki: 15 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。 |
Concentration | Treated Time | Description | References | |
NCI-H716 cells | NCI-H716 cells | 30 min and 6 h | To evaluate the effect of ASP on GLP-1 secretion, results showed that ASP did not directly stimulate GLP-1 secretion. | iScience. 2020 Sep 2;23(9):101522. |
Bone marrow-derived macrophages (BMMs) | Bone marrow-derived macrophages (BMMs) | 5 days | To evaluate the effect of ASP on RANKL-induced osteoclast differentiation. Results showed that ASP dose-dependently reduced the number and size of osteoclasts. | Pharmaceuticals (Basel). 2022 Aug 20;15(8):1027. |
HRVEC cells | HRVEC cells | 1 h | To assess the effect of ASPA on LPS-induced changes in cell connectivity proteins in HRVECs. ASPA reversed the LPS-induced downregulation of ZO-1 and VE-cadherin. | Front Med (Lausanne). 2025 Jan 7;11:1524779. |
ARPE-19 cells | ARPE-19 cells | 1 h | To evaluate the inhibitory effect of ASPA on LPS-induced inflammation in RPE cells. ASPA significantly reduced the mRNA and protein levels of ICAM-1, IL-6, MCP-1, and TNF-α induced by LPS. | Front Med (Lausanne). 2025 Jan 7;11:1524779. |
RAW 264.7 macrophages | RAW 264.7 macrophages | 1 h | Significantly reduced levels of NO, PGE2, TNF-α, and IL-6, inhibited iNOS and COX-2 mRNA and protein expression, exerted anti-inflammatory effects by suppressing NF-κB and MAPK signaling pathways | Int J Mol Sci. 2018 Jul 12;19(7):2027. |
Administration | Dosage | Frequency | Description | References | ||
C57BL/6J mice | High-fat diet-induced obesity and type 2 diabetes model | Oral | 0.25% w/w | 12 weeks | To evaluate the effect of ASP on obesity and type 2 diabetes, results showed that ASP improved obesity and type 2 diabetes by modulating gut microbiota and metabolic signaling. | iScience. 2020 Sep 2;23(9):101522. |
Sprague-Dawley rats | Ligature-induced peri-implantitis model | Intraperitoneal injection | 20 and 40 mg/kg | Every second day for a total of 14 injections | To evaluate the effect of ASP on preventing peri-implantitis. Results showed that ASP delayed the onset time, reduced the morbidity, and decreased alveolar bone resorption around the implant. | Pharmaceuticals (Basel). 2022 Aug 20;15(8):1027. |
Mice | High-fat diet-induced obesity model | Oral | 3 mg/day | Once daily for 12 weeks | To investigate the effects of Asperuloside on body weight, food intake, fat content, blood glucose, and insulin levels in high-fat diet-fed mice. Results showed that Asperuloside significantly reduced body weight (-10.5%) and food intake (-12.8%) in HFD-fed mice, decreased visceral fat mass (-35%), and lowered fasting blood glucose (-16%) and plasma insulin levels (-29%). | Front Endocrinol (Lausanne). 2021 Apr 13;12:615446 |
Sprague Dawley rats | Cadmium-induced nephrocardiac toxicity model | Oral gavage | 50 mg/kg | Once daily for 5 weeks | To investigate the protective effects of asperuloside (ASP) against cadmium-induced nephrocardiac toxicity. The results showed that ASP significantly decreased Cd-instigated oxidative stress, serum BUN, Scr, AST, CK-MB, TnT and LDH levels, as well as histopathological alterations. Furthermore, ASP notably attenuated Cd-induced cardiorenal apoptosis and fibrosis by reducing caspase 3 and TGF-β levels, decreasing the stain intensity of α-SMA and collagen IV, while increasing Bcl2 intensity. | Sci Rep. 2023 Apr 7;13(1):5698 |
Sprague Dawley rats | Endotoxin-induced uveitis (EIU) model | Intravitreal injection | 500 ng/eye | Single injection, lasting 24 hours | To evaluate the anti-inflammatory effect of ASPA in EIU rats. ASPA significantly alleviated clinical symptoms of EIU, reduced inflammatory cell infiltration, and decreased the expression of inflammatory mediators (ICAM-1, IL-6, MCP-1, and TNF-α). | Front Med (Lausanne). 2025 Jan 7;11:1524779. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.41mL 0.48mL 0.24mL |
12.07mL 2.41mL 1.21mL |
24.13mL 4.83mL 2.41mL |
CAS号 | 14259-45-1 |
分子式 | C18H22O11 |
分子量 | 414.36 |
SMILES Code | O=C1O[C@]2([H])[C@@]3([H])[C@](C(COC(C)=O)=C2)([H])[C@H](O[C@H]4[C@@H]([C@H]([C@@H]([C@@H](CO)O4)O)O)O)OC=C13 |
MDL No. | MFCD02094172 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, store in freezer, under -20°C |
溶解方案 |
DMSO: 105 mg/mL(253.4 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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