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4-methoxylonchocarpin

CAS No.: 51589-67-4

4-methoxylonchocarpin was isolated from the roots of Abrus precatorius as a potent anti-inflammatory compound. 4-methoxy
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Description 4-methoxylonchocarpin was isolated from the roots of Abrus precatorius as a potent anti-inflammatory compound. 4-methoxylonchocarpin inhibited NF-κB-activated TNF expression by inhibiting the binding of LPS to TLR4 in macrophages and suppressed TNBS-induced colitis in mice.
In vitro Abrus precatorius(AP, Fabaceae)的根在越南和中国传统上用于治疗炎症性疾病,如口炎、哮喘、支气管炎和肝炎。本研究中,我们分离出4-methoxylonchocarpin (ML)。在脂多糖(LPS)刺激的巨噬细胞中,ML通过抑制LPS与Toll样受体4 (TLR4)的结合,进而抑制核因子(NF)-κB的激活以及肿瘤坏死因子(TNF)和白细胞介素(IL)-6的表达,发挥了作用。[1]
In vivo 小鼠口服4-methoxylonchocarpin(ML)可抑制TNBS引起的结肠炎,表现为减少结肠缩短和结肠中髓过氧化物酶活性的降低。ML处理显著抑制了核因子(NF)-κB的活化和结肠中转化生长因子β激活的激酶1的磷酸化。此外,ML处理还抑制了TNBS诱导的IL-1β、IL-17A和TNF的表达。同时,ML降低了TNBS诱导的M1型巨噬细胞标记物如精氨酸酶-2和TNF的表达,而增加了M2型巨噬细胞标记物如精氨酸酶-1和IL-10的表达。总之,ML通过抑制LPS与免疫细胞上的TLR4的结合并增加M1型巨噬细胞向M2型巨噬细胞的极化,减轻了小鼠的结肠炎。[1]
molecular weight 336.38
Molecular formula C21H20O4
CAS 51589-67-4
Storage store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
References 1. Jang HM, et al. 4-Methoxylonchocarpin attenuates inflammation by inhibiting lipopolysaccharide binding to Toll-like receptor of macrophages and M1 macrophage polarization. Int Immunopharmacol. 2017;45:90-97. 2. Li J, Kang Z, et al. Potent insecticidal activity of Eleocharis dulcis (Burm. f.) Trin peel extract and its main components against aphids. Pest Manag Sci. 2023;79(4):1295-1304. 3. Ngadjui BT, et al. Prenylated flavonoids from the aerial parts of Dorstenia mannii. Phytochemistry. 2000;55(8):915-919. 4. Hussain H, et al. 4-Benzyloxylonchocarpin and Muracatanes A-C from Ranunculus muricatus L. and Their Biological Effects. Biomolecules. 2020;10(11):1562.