Findings indicate that flavonoids from SAC, particularly rhamnocitrin (15), are promising natural neuroprotective candidates for food-based health applications.
Abstract
The seeds of Astragalus complanatus R. Br. (SAC), a medicinal food homologous resource, are widely distributed and utilized in China. A phytochemical investigation of the seeds of SAC afforded 47 flavonoids, including eight previously undescribed ones, designated as complanatin A (2), and neocomplanatosides A-G (38, 39, and 43-47). Among them, 43 and 44 are phenylpropanoid-esterified flavonoid glycosides, while 45-47 represent a rare class of sesquiterpene-esterified flavonoid glycosides. Their structures were elucidated by the NMR and HRESIMS spectroscopic data, and ECD calculations. Biological evaluation demonstrated that rhamnocitrin (15) inhibited ferroptosis in erastin-induced HT22 cells (EC50 = 7.79 ± 0.44 μM) by suppressing NOX4 expression and activating the SLC7A11/Nrf2 pathway. Molecular dynamics simulations confirmed its stable binding to NOX4 (RMSD < 0.4 nm; ΔGbind = - 47.92 kJ/mol), and competitive inhibition with GLX351322 further confirmed NOX4 as the direct target. These findings indicate that flavonoids from SAC, particularly rhamnocitrin (15), are promising natural neuroprotective candidates for food-based health applications.
Chimonanthus salicifolius has traditionally been used for the treatment of gastrointestinal disorders. In this study, a systematic phytochemical investigation of this plant was conducted, leading to the isolation and identification of two previously undescribed furan glycosides, salicifoliosides A (1) and B (2). Struct...
Hui-Zhen Yang, Yi-Wei Wu, Wenjie Shangguan et al.· Chemistry and Biodiversity· 0 citations
Angeloylgomisin O (31) exhibited anti-neuroinflammatory activity by inhibiting lipopolysaccharide (LPS)-induced overproduction of nitric oxide (NO) in BV-2 microglial cells and exhibited notable neuroprotective effects against oxygen-glucose deprivation/reoxygenation (OGD/R)-induced injuries in SH-SY5Y cells.
Fengbei Gong, Pei-Kun Tian, Ning-Yuan Gong et al.· Phytochemistry· 0 citations
Background/Objectives: In the search for potent non-sugar α-glucosidase inhibitors with improved safety profiles, a novel flavonoid glycoside was isolated for the first time from the stem bark of Albizia saponaria (Fabaceae). The objective of this study was to elucidate its chemical structure and evaluate its therapeut...
E. J. Pongoh, R. Rumampuk· Pharmaceuticals· 0 citations
By combining NMR fingerprint with rapid activity screening of eight crude fractions, eleven guanidine alkaloids were obtained from Buthus martensii Karsch, including one new natural product 7 and one new compound 10. Fraction 6 (IC50 = 141.40 ± 0.21 μg/mL) and Fraction 7 (IC50 = 50.89 ± 1.43 μg/mL) showed radical scave...
Astragalus species have long been recognized for their pharmacological relevance, yet the antidiabetic properties of Astragalus cruciatus Link (Ac) remain poorly explored. This study aimed to investigate the antidiabetic potential of A. cruciatus Link and to elucidate possible underlying mechanisms. The ethanolic extra...