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Oxymatrine (Synonyms: Matrine 1oxide)

Catalog No.GN10378 Copy One-Click Copy Product Info

Oxymatrine is a quinolizidine alkaloid extracted from the roots of Sophora flavescens.

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Oxymatrine Chemical Structure

Cas No.: 16837-52-8

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10mM (in 1mL DMSO)
$42.00
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100mg
$39.00
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200mg
$63.00
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500mg
$112.00
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1g
$154.00
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Sample solution is provided at 25 µL, 10mM.



Description of Oxymatrine

Oxymatrine is a quinolizidine alkaloid extracted from the roots of Sophora flavescens[1]. Oxymatrine possesses a wide range of pharmacological activities and exerts anti-inflammatory, anti-fibrotic, and anti-tumor effects mainly by inhibiting iNOS expression and regulating signaling pathways such as TGF-β/Smad and TLR4[2]. Oxymatrine is commonly used in research on liver fibrosis, neuroprotection, and the proliferation and apoptosis mechanisms of various tumor cells[3,4].

In vitro, pretreatment of HUVEC cells with Oxymatrine (2, 4, 8μM) for 1h, followed by continued treatment with oxidized low-density lipoprotein (ox-LDL, 100μg/mL) for 24h, significantly reversed the ox-LDL-induced decrease in cell viability[5]. Treatment of high glucose (55mM glucose)-induced HepG2 cells with Oxymatrine (0.1, 1μM) for 24h dose-dependently reduced glucose production[6].

In vivo, intraperitoneal injection of Oxymatrine (25, 50, 100mg/kg; once daily) for 30 days in C57BL/6J mice infected with Echinococcus multilocularis significantly reduced the wet weight of abdominal cysts[7]. Administration of Oxymatrine (30, 60, 120mg/kg; i.p.) once at 1h before and once at 12h after LPS induction in mice with LPS-induced mastitis significantly reduced the LPS-induced increase in myeloperoxidase (MPO) activity and distribution in mammary tissue at 24h[8].

References:
[1] Chen X, Yi C, Yang X, et al. Liquid chromatography of active principles in Sophora flavescens root[J]. Journal of Chromatography B, 2004, 812(1-2): 149-163.
[2] Wang Y, Hua C, Zhang H, et al. Alkaloids as emerging therapeutics against pulmonary fibrosis: classification, mechanisms, and translational potential[J]. Chemistry & Biodiversity, 2025, 22(12): e01495.
[3] Chai N L, Fu Q, Shi H, et al. Oxymatrine liposome attenuates hepatic fibrosis via targeting hepatic stellate cells[J]. World Journal of Gastroenterology: WJG, 2012, 18(31): 4199.
[4] Dhurandhar Y, Tomar S, Das A, et al. Unlocking the potential of oxymatrine: a comprehensive review of its neuroprotective mechanisms and therapeutic prospects in neurological disorders[J]. ACS Chemical Neuroscience, 2024, 15(23): 4245-4257.
[5] Jin X, Fu W, Zhou J, et al. Oxymatrine attenuates oxidized low-density lipoprotein-induced HUVEC injury by inhibiting NLRP3 inflammasome-mediated pyroptosis via the activation of the SIRT1/Nrf2 signaling pathway[J]. International journal of molecular medicine, 2021, 48(4): 187.
[6] Zhu Y X, Hu H Q, Zuo M L, et al. Effect of oxymatrine on liver gluconeogenesis is associated with the regulation of PEPCK and G6Pase expression and AKT phosphorylation[J]. Biomedical reports, 2021, 15(1): 56.
[7] Zhu Y, Wu P, Wen R, et al. Oxymatrine alleviates Echinococcus multilocularis infection by remodeling the liver immune microenvironment and intestinal flora homeostasis[J]. Frontiers in Cellular and Infection Microbiology, 2025, 15: 1658336.
[8] Yang Z, Yin R, Cong Y, et al. Oxymatrine lightened the inflammatory response of LPS-induced mastitis in mice through affecting NF-κB and MAPKs signaling pathways[J]. Inflammation, 2014, 37(6): 2047-2055.

Protocol of Oxymatrine

Cell experiment [1]:

Cell lines

HUVEC cells

Preparation Method

HUVECs were pre-treated with oxymatrine (2, 4 and 8μM) for 1h prior to ox-LDL (100μg/mL) challenge for 24h at 37℃. Cell viability was measured by CCK-8 assay.

Reaction Conditions

2, 4, and 8μM; 1h and additional 24h

Applications

Oxymatrine (2, 4 and 8μM) significantly reversed the ox-LDL-induced decrease in cell viability. Oxymatrine (4μM) obviously increased the viability of HUVECs treated with ox-LDL, which was selected as an optimal dose for interference with HUVECs treated with ox-LDL.
Animal experiment [2]:

Animal models

C57BL/6J mice infected with E. multilocularis

Preparation Method

Mice were intraperitoneally injected with 2000 E. multilocularis protoscoleces. Three months after infection, mice were treated with Oxymatrine by intraperitoneal injection once daily for 30 consecutive days. After administration, mice were weighed, and abdominal cyst tissues were separated and weighed to calculate cyst wet weight.

Dosage form

25, 50, 100mg/kg; once daily; 30 days; i.p.

Applications

Oxymatrine (25-100mg/kg) significantly reduced abdominal cyst wet weight in E. multilocularis-infected mice.

References:
[1] Jin X, Fu W, Zhou J, et al. Oxymatrine attenuates oxidized low-density lipoprotein-induced HUVEC injury by inhibiting NLRP3 inflammasome-mediated pyroptosis via the activation of the SIRT1/Nrf2 signaling pathway[J]. International journal of molecular medicine, 2021, 48(4): 187.
[2] Zhu Y, Wu P, Wen R, et al. Oxymatrine alleviates Echinococcus multilocularis infection by remodeling the liver immune microenvironment and intestinal flora homeostasis[J]. Frontiers in Cellular and Infection Microbiology, 2025, 15: 1658336.

Chemical Properties of Oxymatrine

Cas No. 16837-52-8 SDF
Synonyms Matrine 1oxide
Chemical Name (41S,7aS,13aR,13bR)-10-oxohexadecahydrodipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridine 4-oxide
Canonical SMILES [O-][N+]12[C@]3([H])[C@@](C([H])([H])C([H])([H])C2([H])[H])([H])[C@](C([H])([H])C([H])([H])C([H])([H])C4=O)([H])N4C([H])([H])[C@]3([H])C([H])([H])C([H])([H])C1([H])[H]
Formula C15H24N2O2 M.Wt 264.36
Solubility DMF: 10 mg/ml,DMSO: 10 mg/ml,Ethanol: 33.3 mg/ml,PBS (pH 7.2): 10 mg/ml Storage Store at -20°C
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Oxymatrine

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1 mg 5 mg 10 mg
1 mM 3.7827 mL 18.9136 mL 37.8272 mL
5 mM 756.5 μL 3.7827 mL 7.5654 mL
10 mM 378.3 μL 1.8914 mL 3.7827 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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