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Asperuloside/车叶草苷 {[allProObj[0].p_purity_real_show]}

货号:A379398

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。

Asperuloside/车叶草苷 化学结构 CAS号:14259-45-1
Asperuloside/车叶草苷 化学结构
CAS号:14259-45-1
Asperuloside/车叶草苷 3D分子结构
CAS号:14259-45-1
Asperuloside/车叶草苷 化学结构 CAS号:14259-45-1
Asperuloside/车叶草苷 3D分子结构 CAS号:14259-45-1
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Asperuloside/车叶草苷 纯度/质量文件 产品仅供科研

货号:A379398 标准纯度: {[allProObj[0].p_purity_real_show]}
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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。

Asperuloside/车叶草苷 细胞实验

Cell Line
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.

Asperuloside/车叶草苷 动物实验

Species
Animal Model
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.

Asperuloside/车叶草苷 实验方案

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

Asperuloside/车叶草苷 技术信息

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

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
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