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SCI-Expanded Özgün Makale Scopus
Chromatographic Analysis and Enzyme Inhibition Potential of Reynoutria japonica Houtt.: Computational Docking, ADME, Pharmacokinetic, and Toxicokinetic Analyses of the Major Compounds
Pharmaceuticals 2025 Cilt 18
Scopus Eşleşmesi Bulundu
18
Cilt
🔓
Açık Erişim
Scopus Yazarları: Tugsen Buyukyildirim, F. Sezer Senol, Osman Tugay, Ramin Ekhteiari Salmas, Onur Kenan Ulutas, Ibrahim Ayhan Aysal, Ilkay Erdogan Orhan
Özet
Background: Reynoutria japonica Houtt. has been used for inflammatory diseases, skin burns, and high cholesterol in traditional Chinese medicine, and the roots and rhizomes of the plant were registered in the Chinese Pharmacopoeia. This study evaluated the enzyme inhibitory activities of R. japonica extracts from Türkiye. Its major phytochemical content was elucidated, molecular interaction studies of the main compounds were conducted, and toxicokinetic predictions and absorption, distribution, metabolism, and elimination studies were performed with in silico methods. Methods: R. japonica extracts were tested for their enzyme inhibitory activities using an ELISA microplate reader. The phytochemical profile was elucidated by LC-MS QTOF. Docking and other in silico studies evaluated interactions of its main components with cholinesterase, collagenase, and elastase. Results: R. japonica exhibited significant cholinesterase inhibitory effectiveness, while the stem and root extracts showed moderate tyrosinase inhibition. R. japonica leaf (IC50 = 117.20 ± 4.84 g/mL) and flower extracts (IC50 = 111.40 ± 1.45 µg/mL) exhibited considerable elastase activity. R. japonica leaf (IC50 = 171.00 ± 6.76 g/mL) and root (IC50 = 160.00 ± 6.81 g/mL) extracts displayed similar and potent collagenase inhibition. In the LC-MS QTOF analysis, procyanidin dimer, catechin, piceid, torachrysone, and its glucoside isomers were identified as the major components and resveratrol as the minor component. Galloylglucose showed the strongest binding at cholinesterase via key hydrogen bonds, while emodin-6-glucoside and emodin formed stable interactions with elastase. Piceid displayed significant polar and water-mediated contacts with collagenase. These findings underscore the potential of these ligands as protein inhibitors. In silico predictions reveal that emodin possessed the most favorable drug-like properties but posed potential interaction risks. Conclusions: This research represents the first investigation of the bioactivity and phytochemistry of R. japonica grown and documented in 2020 in Türkiye. Our findings point out that R. japonica could be used for cosmetic purposes, and further studies on neurological disorders could be performed.
Anahtar Kelimeler (Scopus)
docking simulations enzyme inhibition in silico ADME in silico toxicokinetic LC-MS QTOF piceid resveratrol Reynoutria japonica

Anahtar Kelimeler

docking simulations enzyme inhibition in silico ADME in silico toxicokinetic LC-MS QTOF piceid resveratrol Reynoutria japonica

Makale Bilgileri

Dergi Pharmaceuticals
ISSN 1424-8247
Yıl 2025 / 3. ay
Cilt / Sayı 18
Makale Türü Özgün Makale
Hakemlik Hakemli
Endeks SCI-Expanded
Yayın Dili Türkçe
Kapsam Uluslararası
Toplam Yazar 7 kişi
Erişim Türü Basılı+Elektronik
Erişim Linki Makaleye Git
Alan Sağlık Bilimleri Temel Alanı Farmakognozi

YÖKSİS Yazar Kaydı

Yazar Adı BÜYÜKYILDIRIM TUĞSEN,ŞENOL DENİZ FATMA SEZER,TUGAY OSMAN,Salmas Ramin Ekhteiari,ULUTAŞ ONUR KENAN,Aysal Ibrahim Ayhan,ERDOĞAN ORHAN İLKAY
YÖKSİS ID 8603796