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In vitro and in silico anti-inflammatory effect of minor constituents from the roots of Polygala arillata Buch.-Ham. ex D. Don
被引:0
|作者:
Luyen, Bui Thi Thuy
[1
]
Quang, Tran Anh
[2
]
Duy, Le Xuan
[2
]
Tai, Bui Huu
[3
]
Phong, Nguyen Viet
[3
,10
,11
]
Nghi, Do Huu
[4
]
Khoi, Nguyen Minh
[2
]
Chinh, Nguyen Van
[5
]
Cuong, Nguyen Cao
[5
]
Thuy, Trinh Thi
[6
]
Huong, Tran Thu
[7
]
Vinh, Le Ba
[8
]
Anh, Nguyen Hong
[9
]
Hiep, Nguyen Tuan
[2
]
机构:
[1] Hanoi Univ Pharm, Fac Pharmaceut Chem & Technol, Dept Pharmaceut Chem Technol & Extract, Hanoi, Vietnam
[2] Natl Inst Med Mat, 3B-Quang trung, Hanoi, Vietnam
[3] Vietnam Acad Sci & Technol VAST, Inst Marine Biochem, Hanoi, Vietnam
[4] VAST, Inst Nat Prod Chem, Hanoi, Vietnam
[5] Yersin Univ Da Lat, Fac Med & Pharm, Lam Dong, Vietnam
[6] VAST, Inst Chem, Hanoi, Vietnam
[7] Hanoi Univ Sci & Technol, Sch Chem & Life Sci, Hanoi, Vietnam
[8] Bergen Univ, Dept Chem, N-5007 Bergen, Norway
[9] VAST, Inst Sci & Technol Energy & Environm, Hanoi, Vietnam
[10] Kyungpook Natl Univ, teachers Coll, Dept Biol Educ, Daegu, South Korea
[11] Kyungpook Natl Univ, Inst Phylogen & evolut, Daegu, South Korea
关键词:
<italic>Polygala arillata</italic>;
polygarinolide A;
anti-inflammatory effect;
TENUIFOLIA;
D O I:
10.1080/14786419.2024.2429121
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Vietnamese traditional medicine has utilised the roots of Polygala arillata Buch.-Ham. ex D. Don to treat acute arthritis, rheumatism, pain, and as a tonic ingredient. In this study, phytochemical analysis of the roots of P. arillata resulted in the isolation of one novel compound, named polygarinolide A (1), along with six known compounds (2-7). High-resolution electrospray ionisation mass spectrometry (HR-ESI-MS) and one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy were among the spectroscopic techniques used to identify their structures. Additionally, the absolute configuration of compound 1 was determined through ECD calculation. The NO inhibitory activity of purified substances was evaluated. Interestingly, compound 2 exhibited inhibitory activity on NO production in LPS-stimulated RAW264.7 cells (IC50 = 25.37 mu M). Moreover, interactions and binding mechanisms of the most active chemical with cyclooxygenase-2 inhibitor (COX-2) and nitric oxide synthase (iNOS) proteins were investigated by molecular docking simulations. Our findings add to our understanding of the secondary metabolites generated by P. arillata and provide a sound scientific basis for future research into the plant's potential anti-inflammatory properties.
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