2019
DOI: 10.29244/avl.3.4.79-80
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Studi in silico potensi anthelmintik rambusa (Passiflora foetida) sebagai inhibitor produksi ATP pada Ascaris suum

Abstract: Resistensi terhadap anthelmintika memacu upaya penemuan anthelmintika baru yang bekerja melalui penghambatan produksi energi ATP anaerobik pada sel parasit. Parasit melakukan metabolisme menggunakan enzim fumarat reduktase yang berfungsi untuk mengubah fumarat menjadi suksinat. Reaksi fumarat reduktase terjadi di mitokondria dengan bantuan rhodoquinone. Mitochondrial rhodoquinol-fumarate reductase  dianggap sebagai target reseptor yang baik untuk pengembangan anthelmintik baru. Penelitian ini bertujuan untuk m… Show more

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“…This stage was carried out using AutoDock and Notepad++ software. The minimization stage aims to convert the compound from .sdf to .pdb format through the PyRx software in order to make the ligand more flexible and produce the lowest binding energy when docked [13] Structure preparation of active compounds and drugs was carried out to stabilize the 3D structure because a stable structure will minimize the energy involved in pharmacokinetic and pharmacodynamic testing, where penicillin-type antibiotic drugs are used as comparators [14]. The drug effect can be determined by the concentration of the drug on its target receptor and the pharmacodynamic effect of the interaction of the receptor with the drug [15].…”
Section: Methodsmentioning
confidence: 99%
“…This stage was carried out using AutoDock and Notepad++ software. The minimization stage aims to convert the compound from .sdf to .pdb format through the PyRx software in order to make the ligand more flexible and produce the lowest binding energy when docked [13] Structure preparation of active compounds and drugs was carried out to stabilize the 3D structure because a stable structure will minimize the energy involved in pharmacokinetic and pharmacodynamic testing, where penicillin-type antibiotic drugs are used as comparators [14]. The drug effect can be determined by the concentration of the drug on its target receptor and the pharmacodynamic effect of the interaction of the receptor with the drug [15].…”
Section: Methodsmentioning
confidence: 99%