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Determination of phenolic contents by HPLC, and antioxidant, antimicrobial, antityrosinase, and anticholinesterase activities of psephellus huber-morathii

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info:eu-repo/semantics/openAccess

Date

2019

Author

Korkmaz, Nuriye
Şener, Sıla Özlem
Baltürk, Nuray
Kanbolat, Şeyda
Badem, Merve
Aliyazıcıoğlu, Rezzan
Özgen, Ufuk
Kandemir, Ali
Karaoğlu, Şengül Alpay

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Citation

Korkmaz, N., Sener, S. O., Balturk, N., Kanbolat, S., Badem, M., Aliyazicioglu, R., Ozgen, U., Kandemir, A., & Karaoglu, S. A. (2019). Determination of Phenolic Contents by HPLC, and Antioxidant, Antimicrobial, Antityrosinase, and Anticholinesterase Activities of Psephellus huber-morathii. Journal of Pharmaceutical Research International, 26(1), 1–10. https://doi.org/10.9734/jpri/2019/v26i130125

Abstract

The goal of our study was to examine of antioxidant, antimicrobial, anticholinesterase activities, and phenolic composition of Psephellus huber-morathii. the antioxidant activities of extracts have been assessed by Ferric reducing antioxidant power (FRAP), cupric reducing antioxidant capacity (CUPRAC), and 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging. Phenolic constituents were measured using reverse phase-high performance liquid chromatography (RP-HPLC), and antimicrobial activity was investigated using the agar well diffusion method. Total phenolic content, FRAP, and CUPRAC results of aqueous extract have been better than methanolic extract, except for DPPH activity. Benzoic acid, and p-coumaric acid as major phenolic compounds were specified. Methanolic extract was especially effective against all microorganisms tested except for Yersinia pseudotuberculosis. the methanolic extract have been displayed inhibitory effect on tyrosinase. All extracts have been exhibited lower acetylcholinesterase, and butyrylcholinesterase inhibitory activities than galantamine. P. huber-morathii can be considered in the food, and drug industries due to antioxidant capacity and antimicrobial activities of the species. It can be potential source as anti-browning agents because of its average tyrosinase inhibitory activity.

Source

Journal of Pharmaceutical Research International

Volume

26

Issue

1

URI

https://doi.org/10.9734/JPRI/2019/v26i130125
https://hdl.handle.net/11436/1669

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  • FEF, Biyoloji Bölümü Koleksiyonu [594]
  • WoS İndeksli Yayınlar Koleksiyonu [5260]



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