Browsing by Author "Aisyah, Fadila"

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    SINTESIS, UJI AKTIVITAS ANTIDIABETES DAN STUDI MOLECULAR DOCKING SENYAWA PIRIDAZINON 6-(3-BROMOFENIL)-2- (FENILSULFONIL)PIRIDAZIN-3(2H)-ON
    (perpustakaan UR, 2021-07) Aisyah, Fadila; Zamri, Adel
    Pyridazinone is oxo-pyridazine derivative compound that has broad bioactivity, such as an analgesic, anti-inflammatory, antidiabetic, antihypertensive and anticancer. Pyridazinone 6- (3-bromophenyl)-2-(phenylsulfonyl)pyridazine-3(2H)-one was synthesized from 6-(3- bromophenyl)pyridazine-3(2H)-one through a Claisent-Schmidt condensation reaction between 3-bromo acetophenone and glyoxylic acid then a cyclization reaction occurs with hydrazine hydrate. The pyridazinone compound formed is substituted with the benzensulfonyl chloride. The structure of the synthesized compound was confirmed by characterization using UV, FTIR, 1H-NMR and HRMS spectroscopy. Pyridazinone compounds were tested for their antidiabetic activity through molecular docking and in vitro studies. A molecular docking study was performed on the crystal structure of human lysosomal α-glucosidase (PDB ID: 5NN5) and compared with acarbose as a positive control. The activity of the PDZ-3Br-BZS compound was less good activity in inhibiting the α-glucosidase enzyme, which is 2.481% and confirmed by molecular docking studies that it only has one hydrogen bond interaction in common with acarbose, that is with the amino acid Asp 616 and a large bond free energy of -10 ,9567 kcal/mol compared to acarbose which is -18,2395 kcal/mol.