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Image of SKRINING SENYAWA METABOLIT SEKUNDER Lansium domesticum Corr. YANG BERPOTENSI SEBAGAI ANTIDIABETIK TERHADAP ENZIM α-glukosidase SECARA IN SILICO

Skripsi

SKRINING SENYAWA METABOLIT SEKUNDER Lansium domesticum Corr. YANG BERPOTENSI SEBAGAI ANTIDIABETIK TERHADAP ENZIM α-glukosidase SECARA IN SILICO

Nadilla, Putri - Personal Name;

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Diabetes mellitus is a disease that experiences an increase in the number of sufferers every year with treatment from synthetic ingredients that can cause harmful side effects to the body. Therefore, the discovery of a natural source of materials from Lansium domesticum Corr. that can inhibit the work of the enzyme α-glucosidase has emerged. Inhibition of the action of diabetes enzymes is one of the potential targets in controlling sugar levels. The enzyme α-glucosidase can be done by inhibiting the active side of the enzyme so that it can slow down the digestion and absorption of carbohydrates. Molecular docking can predict the interaction between compounds from Lansium domesticum Corr. and the target protein enzyme α-glucosidase in silico. Therefore, it is important to search for metabolite compounds from Lansium domesticum Corr. that have the potential to be antidiabetic in inhibiting the enzyme α-glucosidase by producing the lowest binding affinity value and a group of compounds from ligands that can bind to receptors are carried out in silico which can be utilized by having physicochemical, pharmacokinetic biological activity and safe from toxicity. It was carried out by an experimental method in silico to obtain the binding affinity interaction between ligands from Lansium domesticum Corr. compounds and α-glucosidase enzyme receptors safely. The resulting 38 secondary metabolite compounds of Lansium domesticum Corr. have biological activity as an antidiabetic by inhibiting the action of the enzyme α-glucosidase. Based on physicochemical, pharmacokinetic, and toxicity predictions from 38 compounds, 4 Lansium domesticum Corr. test compounds were obtained that were safe to be antidiabetic candidates, namely Catechin, Aphanamol II, Spathulenol and Isogemacrene D were able to inhibit the active side of the enzyme α-glucosidase in silico. Keyword: Antidiabetic, Lansium domesticum Corr., α-glucosidase, in silico, Molecular docking.


Availability
Inventory Code Barcode Call Number Location Status
2507002384T171233T1712332025Central Library (Reference)Available but not for loan - Not for Loan
Detail Information
Series Title
-
Call Number
T1712332025
Publisher
Indralaya : Prodi Ilmu Biologi, Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Sriwijaya., 2025
Collation
xv, 85 hlm.; ilus.; tab.; 29 cm.
Language
Indonesia
ISBN/ISSN
-
Classification
547.707
Content Type
Text
Media Type
-
Carrier Type
-
Edition
-
Subject(s)
Metabolit Enzim
Specific Detail Info
-
Statement of Responsibility
MI
Other version/related

No other version available

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  • SKRINING SENYAWA METABOLIT SEKUNDER Lansium domesticum Corr. YANG BERPOTENSI SEBAGAI ANTIDIABETIK TERHADAP ENZIM α-glukosidase SECARA IN SILICO
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