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SCI-Expanded JCR Q1 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 Sayı 3
Scopus Eşleşmesi Bulundu
3
Atıf
18
Cilt
🔓
Açık Erişim
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.
Web of Science Eşleşmesi Bulundu
3
WoS Atıf
18
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Article
Belge Türü
Kaynak: PHARMACEUTICALS
Anahtar Kelimeler (WoS)

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Scimago Dergi Bilgisi Otomatik ISSN Eşleştirmesi 2025 yılı verileri
Pharmaceuticals
Q1
SJR Quartile
1,140
SJR Skoru
120
H-Index
🔓
Açık Erişim
Kategoriler: Drug Discovery (Q1) · Pharmaceutical Science (Q1) · Molecular Medicine (Q2)
Alanlar: Biochemistry, Genetics and Molecular Biology · Pharmacology, Toxicology and Pharmaceutics
Ülke: Switzerland · Multidisciplinary Digital Publishing Institute (MDPI)
Bu bilgiler makale yılına göre Scimago veritabanından ISSN eşleştirmesiyle otomatik getirilmektedir. Dergi sıralama verileri Scimago'nun ilgili yılı baz alınmaktadır.

Anahtar Kelimeler

Makale Bilgileri

Dergi Pharmaceuticals
ISSN 1424-8247
Yıl 2025 / 1. ay
Cilt / Sayı 18 / 3
Makale Türü Özgün Makale
Hakemlik Hakemli
Endeks SCI-Expanded
JCR Quartile Q1
Teşvik Puanı 2,57 · YÖKSİS Akademik Teşvik
Yayın Dili Türkçe
Kapsam Uluslararası
Toplam Yazar 7 kişi
Alan Sağlık Bilimleri Temel Alanı Farmasotik Botanik

YÖKSİS Yazar Kaydı

Yazar Adı BÜYÜKYILDIRIM TUĞSEN,ŞENOL DENİZ FATMA SEZER,TUGAY OSMAN,Salmas Ramin Ekhteiari,ULUTAŞ ONUR KENAN,Aysal İbrahim Ayhan,ERDOĞAN ORHAN İLKAY
YÖKSİS ID 8671606

Metrikler

Scopus Atıf 3
Havuz Atıfları 0
JCR Quartile Q1
Teşvik Puanı 2,57
Yazar Sayısı 7