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Atıf Alan Yayın
In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical profile of Potentilla thuringiaca
Phytochemistry Letters Cilt 20 ss. 365-372
Scopus Toplam 432 atıf DOI
The genus Potentilla is interesting for the pharmaceutical field due to its valuable medicinal properties, which have been observed in complementary and alternative medicine. In recent years, studies conducted to estimate the biological activity of several of the Potentilla species have shown a wide spectrum of therapeutic properties. In particular, in the present paper, different extracts obtained from the herb P. thuringiaca were analysed for antioxidant and enzyme inhibitory activities. The UHPLC-DAD-MS3 hyphenated techniques reported herein allow for the identification of phytoconstituents. The analyses showed the presence of flavonoids and ellagitannins as major components. Furthermore, the data demonstrated that the analysed extracts revealed a high total antioxidant capacity in the phosphomolybdenum assay. The free radical scavenging activity of the extracts was evaluated using DPPH and ABTS assays. The reducing power activity of P. thuringiaca was also determined by FRAP and CUPRAC assays, as well as metal chelating activity. In addition, the total extracts and the different fractions of P. thuringiaca revealed potent inhibitory activities against α-amylase and α-glucosidase, AChE, tyrosinase and lipase. Surprisingly, no activity against BChE was shown. P. thuringiaca could be a valuable natural source of antioxidants with interesting inhibitory actions against the key enzymes involved in several human diseases, and could represent a valid starting point for the development of new treatment and management strategies, including its use as a food supplement.
Atıf Kaynağı
Atıf Yapan Yayın
Phytochemical characterization and multi-biological potentials of Inula viscosa: New in vitro evidence
Zeitschrift Fur Naturforschung Section C Journal of Biosciences Cilt 81 ss. 503-525
Scopus Havuzumuzda
Inula viscosa is a common medicinal plant and is mostly spread in Mediterranean countries. The current study analyses I. viscosa extracts for antimicrobial capacity, phenolic content, antioxidant, enzyme inhibition, and molecular modeling. The extracts' anticancer potential in prostate and breast cancer cells was evaluated, and their anti-metastatic and molecular activities were analyzed through gene expression. The most prevalent substances in the methanol extract of I. viscosa are phenolic acids, which include derivatives of caffeic acid and mono-, di-, and tri-caffeoylquinic acids. Dicaffeoylquinic acids represented 88% of the quantified phenolics. The methanol extract showed a 50% inhibitor concentration (IC50) of 101.4μg/mL at 48h in PC3 cells. Autophagy-related genes were found to be down-regulated in all three cancer cells. Regarding antimetastatic activity, the wound width remained ∼96% at 48h after ethyl acetate treatment in MCF-7cells. The water extract had the highest total phenolic content and the strongest antioxidant capacity, followed by the methanol extract. Modest binding potential to B-cell leukemia-2 (Bcl-2) was observed with caffeoylquinic acid and caffeic acid derivatives, which may be related to pro-apoptotic/anticancer effects. Our results suggested that I. viscosa can be considered as an effective raw material for designing health-promoting applications.
Atıf Yapan Makale Bilgileri
Kurumlar (5)
İstanbul Arel Üniversitesi Istanbul, Turkey
Kastamonu University Kastamonu, Turkey
Medical University of Sofia Sofia, Bulgaria
Selçuk Üniversitesi Selçuklu, Turkey
Universidad de Jaén Jaen, Spain