Journal Articles - Natural Science - 2021

Permanent URI for this collection

http://repository.vlu.edu.vn:443/handle/123456789/114

Browse

Browsing Journal Articles - Natural Science - 2021 by Author "Dao-Cuong To"
  • Publication
    On the Inhibitability of Natural Products Isolated from Tetradium ruticarpum towards Tyrosine Phosphatase 1B (PTP1B) and α-Glucosidase (3W37): An In Vitro and In Silico Study
    ( 2021)
    Dao-Cuong To
    ;
    Thanh Q. Bui
    ;
    Nguyen Thi Ai Nhung
    ;
    Quoc-Toan Tran
    ;
    Thi-Thuy Do
    ;
    Manh-Hung Tran
    ;
    Phan-Phuoc Hien
    ;
    Truong-Nhan Ngu
    ;
    Phan-Tu Quy
    ;
    The-Hung Nguyen
    ;
    Huu-Tho Nguyen
    ;
    Tien-Dung Nguyen
    ;
    Phi-Hung Nguyen
    Folk experiences suggest natural products in Tetradium ruticarpum can be effective inhibitors towards diabetes-related enzymes. The compounds were experimentally isolated, structurally elucidated, and tested in vitro for their inhibition effects on tyrosine phosphatase 1B (PTP1B) and α-glucosidase (3W37). Density functional theory and molecular docking techniques were utilized as computational methods to predict the stability of the ligands and simulate interaction between the studied inhibitory agents and the targeted proteins. Structural elucidation identifies two natural products: 2-heptyl-1-methylquinolin-4-one (1) and 3-[4-(4-methylhydroxy-2-butenyloxy)-phenyl]-2-propenol (2). In vitro study shows that the compounds (1 and 2) possess high potentiality for the inhibition of PTP1B (IC50 values of 24.3 ± 0.8, and 47.7 ± 1.1 μM) and α-glucosidase (IC50 values of 92.1 ± 0.8, and 167.4 ± 0.4 μM). DS values and the number of interactions obtained from docking simulation highly correlate with the experimental results yielded. Furthermore, in-depth analyses of the structure–activity relationship suggest significant contributions of amino acids Arg254 and Arg676 to the conformational distortion of PTP1B and 3W37 structures overall, thus leading to the deterioration of their enzymatic activity observed in assay-based experiments. This study encourages further investigations either to develop appropriate alternatives for diabetes treatment or to verify the role of amino acids Arg254 and Arg676.