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Metabolites of Pinang Yaki (Areca vestiaria) Fruit Extract: A Metabolite Profiling Study

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Background:  Pinang yaki has bioactive compounds that have potential as a new herbal supplement, but their metabolites profil is lack of data. A better understanding of the bioactive compounds of pinang yaki using untargeted metabolomic profiling studies will provide clearer insight into the health benefits of pinang yaki in further.   Methods:  Fresh samples of pinang yaki ( Areca vestiaria ) are obtained from forests in North Sulawesi Province, Indonesia. Samples were used for untargeted metabolomics analysis by UHPLC-MS.   Results:  Based on an untargeted metabolomic profiling study of pinang yaki, 2504 compounds in ESI- and 2645 compounds in ESI+ were successfully obtained. After the analysis, 356 compounds in ESI- and 543 compounds in ESI+ were identified successfully. Major compounds Alpha-Chlorohydrin (PubChem ID: 7290) and Tagatose (PubChem ID: 439312) were found in ESI+ and ESI-.   Discussion:  The 10 metabolites from pinang yaki extract (ESI+) also have been indicated in preventing viral infection and have exhibited good neuroprotective immunity. Benzothiazole (PubChem ID: 7222), L-isoleucine (PubChem ID: 6306), D-glucono-delta-lactone (PubChem ID: 736), Diethylpyrocarbonate (PubChem ID: 3051), Bis(2-Ethylhexyl) amine (PubChem ID: 7791), Cinnamic acid (PubChem ID: 444539), and Trigonelline (PubChem ID: 5570) also had potential effects as an antiviral and anti-inflammatory. Conclusion:  Untargeted metabolomic profiling showed many bioactive compounds contained in pinang yaki ( Areca vestiaria ) extract. The top 10 compounds capable to ionize well have been identified and explored for their potential benefits as antiviral supplement products by literature study. This is a preliminary study which still needs further research such as in vitro, preclinical, and clinical trials.
Title: Metabolites of Pinang Yaki (Areca vestiaria) Fruit Extract: A Metabolite Profiling Study
Description:
Background:  Pinang yaki has bioactive compounds that have potential as a new herbal supplement, but their metabolites profil is lack of data.
 A better understanding of the bioactive compounds of pinang yaki using untargeted metabolomic profiling studies will provide clearer insight into the health benefits of pinang yaki in further.
   Methods:  Fresh samples of pinang yaki ( Areca vestiaria ) are obtained from forests in North Sulawesi Province, Indonesia.
Samples were used for untargeted metabolomics analysis by UHPLC-MS.
   Results:  Based on an untargeted metabolomic profiling study of pinang yaki, 2504 compounds in ESI- and 2645 compounds in ESI+ were successfully obtained.
After the analysis, 356 compounds in ESI- and 543 compounds in ESI+ were identified successfully.
 Major compounds Alpha-Chlorohydrin (PubChem ID: 7290) and Tagatose (PubChem ID: 439312) were found in ESI+ and ESI-.
   Discussion:  The 10 metabolites from pinang yaki extract (ESI+) also have been indicated in preventing viral infection and have exhibited good neuroprotective immunity.
Benzothiazole (PubChem ID: 7222), L-isoleucine (PubChem ID: 6306), D-glucono-delta-lactone (PubChem ID: 736), Diethylpyrocarbonate (PubChem ID: 3051), Bis(2-Ethylhexyl) amine (PubChem ID: 7791), Cinnamic acid (PubChem ID: 444539), and Trigonelline (PubChem ID: 5570) also had potential effects as an antiviral and anti-inflammatory.
Conclusion:  Untargeted metabolomic profiling showed many bioactive compounds contained in pinang yaki ( Areca vestiaria ) extract.
 The top 10 compounds capable to ionize well have been identified and explored for their potential benefits as antiviral supplement products by literature study.
 This is a preliminary study which still needs further research such as in vitro, preclinical, and clinical trials.

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