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Macelignan/安五脂素 {[allProObj[0].p_purity_real_show]}

货号:A456389 同义名: (+)-Anwulignan; Anwuligan

Anwuligan 是从五味子(Schisandra chinensis)果实中分离和纯化的天然产物,具有对抗氧化应激和神经炎症的神经退行性疾病的治疗潜力。

Macelignan/安五脂素 化学结构 CAS号:107534-93-0
Macelignan/安五脂素 化学结构
CAS号:107534-93-0
Macelignan/安五脂素 3D分子结构
CAS号:107534-93-0
Macelignan/安五脂素 化学结构 CAS号:107534-93-0
Macelignan/安五脂素 3D分子结构 CAS号:107534-93-0
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Macelignan/安五脂素 纯度/质量文件 产品仅供科研

货号:A456389 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 COX COX-1 COX-2 其他靶点 纯度
Piroxicam 98%
Salicylic acid 98%
Phenacetin 98%
Etodolac 99%
Flunixin meglumine 98%
Ibuprofen L-lysine 98%
Nabumetone 98%
Acemetacin 98%
Diflunisal 98%
Pranoprofen 98%
Ampiroxicam 98%
Meloxicam 98%
Sulindac 98%
Ketoprofen 98%
Mefenamic Acid 95%
Bromfenac sodium 98%
Oxaprozin 99%
Aspirin 99%
Nepafenac 98%
Zaltoprofen 99%
Salicin 98%
Suprofen 99%+
Xanthohumol 99%
Parecoxib 98%
Tolfenamic Acid +++

COX-2, IC50: 0.2 μM

98%
Etoricoxib 99%
Niflumic Acid 98%
Valdecoxib ++++

COX-2, IC50: 5 nM

99+%
Ibuprofen +

COX-1, IC50: 13 μM

+

COX-2, IC50: 370 μM

98%
Indomethacin ++

COX1, IC50: 0.28 μM

+

COX-2, IC50: 14 μM

97%
Lornoxicam ++++

COX-1, IC50: 5 nM

++++

COX-2, IC50: 8 nM

98%
Meclofenamic acid sodium ++++

COX-1, IC50: 40 nM

+++

COX-2, IC50: 50 nM

99%
Asaraldehyde 98%
Naproxen +

COX-1, IC50: 8.7 μM

+

COX-2, IC50: 5.2 μM

98%
Diclofenac Sodium Salt +++

COX-1, IC50: 60 nM

+++

COX-2, IC50: 200 nM

98%
NS-398 ++

COX-2, IC50: 3.8 μM

95%
Amfenac Sodium Hydrate ++

COX-1, IC50: 250 nM

+++

COX-2, IC50: 150 nM

98%+
Nimesulide +

COX-2, IC50: 26 μM

98%
Lumiracoxib ++

COX-1, Ki: 3 μM

+++

COX-2, Ki: 60 nM

98%
Rutaecarpine 95%
Celecoxib ++++

COX-2, IC50: 40 nM

98%
Carprofen ++++

canine COX2, IC50: 30 nM

98%
Ketorolac ++

COX-1 (human), IC50: 1.23 μM

++

COX-2 (human), IC50: 3.50 μM

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。

Macelignan/安五脂素 生物活性

描述 Anwuligan, a natural product isolated and purified from the fruits of Schisandra chinensis, possesses therapeutic potentials against neurodegenerative diseases with oxidative stress and neuroinflammation.

Macelignan/安五脂素 细胞实验

Cell Line
Concentration Treated Time Description References
3×Transgene-AD mouse primary neuron cells 20 µM 24 hours To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 404 site Front Nutr. 2022 May 18;9:892558
N2a/SweAPP cells 0, 5, 10, 15, 20 µM 24 hours To investigate the effect of Macelignan on Aβ aggregation, results showed that Macelignan significantly reduced the expression levels of APP and Aβ Front Nutr. 2022 May 18;9:892558
HEK293/Tau cells 0, 5, 10, 15, 20 µM 24 hours To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 396, Ser 404, and Thr 231 sites Front Nutr. 2022 May 18;9:892558
SH-SY5Y/Tau cells 0, 5, 10, 15, 20 µM 24 hours To investigate the effect of Macelignan on Tau phosphorylation, results showed that Macelignan significantly reduced the phosphorylation levels of Tau at Ser 396, Ser 404, and Thr 231 sites Front Nutr. 2022 May 18;9:892558
MCF-7 cells 100 µM 144 hours To evaluate the effect of Macelignan on the proliferation of MCF-7 cells, results showed that 100 µM Macelignan increased cell proliferation to 201.07 ± 3.68% Pharmaceutics. 2021 Jul 15;13(7):1082
H9c2 cardiomyoblast cells 50 μM 22 hours To evaluate the protective effect of Macelignan against H2O2-induced oxidative stress, results showed that Macelignan significantly improved cell viability and reduced apoptosis Sci Rep. 2021 Jan 12;11(1):664
HepG2 cells 0–3 mM 48h Assess the cytotoxicity of Macelignan on HepG2 cells, showing low cytotoxicity. Braz J Med Biol Res. 2016 Jul 4;49(7):e5313
Ascosphaera apis 1.56 mg/mL (24h), 3.125 mg/mL (48h) 24h, 48h Evaluate the antifungal activity of Macelignan against Ascosphaera apis, showing significant growth inhibition. Braz J Med Biol Res. 2016 Jul 4;49(7):e5313
Streptococcus sanguinis 200 µg/ml 24 hours To evaluate the growth inhibitory effect of Macelignan on Streptococcus sanguinis, showing an inhibition zone diameter of 12.2±1.13 mm. Oral Health Prev Dent. 2020 Jul 4;18(3):537-542
Streptococcus mutans 200 µg/ml 24 hours To evaluate the growth inhibitory effect of Macelignan on Streptococcus mutans, showing an inhibition zone diameter of 11.8±0.67 mm. Oral Health Prev Dent. 2020 Jul 4;18(3):537-542

Macelignan/安五脂素 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice Chronic unpredictable mild stress (CUMS) model Intragastric administration 5 mg/kg Daily administration for 30 days Macelignan significantly improved CUMS-induced depression-like behaviors, including reduced immobility time in forced swimming and tail suspension tests. Additionally, Macelignan restored oxidative balance, suppressed neuroinflammation, and enhanced synaptic plasticity. Transl Psychiatry. 2025 May 9;15(1):163

Macelignan/安五脂素 参考文献

[1]Yang X, Xiang Q, Chen J. [Selection of mobile phases for the determination of gamma-schisandrin and multi-active constituents in Schisandra chinensis and its preparations by high performance liquid chromatography] . Se Pu. 2009 May;27(3):313-7. Chinese.

Macelignan/安五脂素 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.05mL

0.61mL

0.30mL

15.23mL

3.05mL

1.52mL

30.45mL

6.09mL

3.05mL

Macelignan/安五脂素 技术信息

CAS号107534-93-0
分子式C20H24O4
分子量 328.4
SMILES Code OC1=CC=C(C[C@H](C)[C@H](C)CC2=CC=C(OCO3)C3=C2)C=C1OC
MDL No. MFCD09953803
别名 (+)-Anwulignan; Anwuligan
运输蓝冰
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: 105 mg/mL(319.73 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
方案 三
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