Antioxidant activity, anti-tyrosinase activity, molecular docking studies, and molecular dynamic simulation of active compounds found in nipa palm vinegar

Author:

Chatatikun Moragot12,Tedasen Aman13,Pattaranggoon Nawanwat Chainuwong45,Palachum Wilawan12,Chuaijit Sirithip6,Mudpan Amron1,Pruksaphanrat Supawita1,Sohbenalee Sasirat1,Yamasaki Kenshi7,Klangbud Wiyada Kwanhian12

Affiliation:

1. Department of Medical Technology, School of Allied Health Sciences, Walailak University, Thasala, Nakhon Si Thammarat, Thailand

2. Center of Excellence Research of Melioidosis and Microorganisms, Walailak University, Thasala, Nakhon Si Thammarat, Thailand

3. Research Excellence Center of Innovation and Health Products, Walailak University, Thasala, Nakhon Si Thammarat, Thailand

4. Program in Bioinformatics and Computational Biology, Chulalongkorn University, Bangkok, Thailand

5. Faculty of Medical Technology, Rangsit University, Muang Pathumthani, Pathumthani, Thailand

6. School of Medicine, Walailak University, Thasala, Nakhon Si Thammarat, Thailand

7. Department of Dermatology, Graduate School of Medicine, Tohoku University, Sendai, Japan

Abstract

Tyrosinase is a key enzyme in melanogenesis and its inhibitors have become increasingly because of their potential activity as hypopigmenting agents which have less side effects. Nipa palm vinegar is an aqueous product that is normally used as a food supplement. The aim of this study was to study the determination of antioxidant activity and tyrosinase inhibitory activities of aqueous extract of original nipa palm vinegar (AE O-NPV), nipa palm vinegar powder (NPV-P) and aqueous extract of nipa palm vinegar powder (AE NPV-P) were examined. Nipa palm vinegars were evaluated the phenolic and flavonoid content, and the active compounds which were submitted to molecular docking and molecular dynamic simulation, chemoinformatics, rule of five, skin absorption and toxicity. The highest phenolic and flavonoid contents in the AE O-NPV were 2.36 ± 0.23 mg gallic acid equivalents/g extract and 5.11 ± 0.59 mg quercetin equivalents/g, and the highest ABTS radical cation scavenging activity was also found. The AE O-NPV, NPV-P and AE NPV-P showed anti-mushroom tyrosinase activity. The HPLC analysis showed that there were vanillic acid and three flavonoids (catechin, rutin and quercetin). The molecular docking study revealed that the binding of the vanillic acid and three flavonoids occurred in the active site residues (histidine and other amino acids). Moreover, the number of hydrogen bond acceptors/donors, solubility, polar surface area and bioavailability score of the vanillic acid and three flavonoids were acceptable compared to Lipinski’s Rule of Five. The molecular dynamic simulation showed that vanillic acid interacts with HIS284 through ππ stacking hydrophobic interactions and forms a metal-acceptor interaction with the copper molecule at the tyrosinase active site. All compounds revealed good skin permeability and nontoxicity. Nipa palm vinegar could be a promising source of a new ingredient for tyrosinase inhibition for cosmetics or pharmaceutical products.

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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