Phenolic Compounds from <i>Diarthron iranica</i>: Enzymatic and in Silico Insights Into α-Amylase Inhibitory Activity

The phytochemical analysis carried out on the aerial parts of <i>D. iranica</i> yielded the identification and characterization of four phenolic compounds, including a methoxy apigenin glycoside (1), one bicoumarin (2), and two lignans (3-4). Molecular docking studies indicated that compound 1 exhibited superior inhibitory potential compared to compound 3, with stable interactions in the enzyme's binding site. In α-amylase inhibitory assays, these compounds displayed varying levels of activity, with compound 2 showing the highest potency (IC<sub>50</sub> = 0.71 mg/mL), followed by compounds 1 (IC<sub>50</sub> = 1.32 mg/mL) and 3 (IC<sub>50</sub> = 1.81 mg/mL). However, all were less effective than the reference compound luteolin (IC<sub>50</sub> = 0.63 mg/mL), which demonstrated superior efficacy.

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Publication Details

Journal
Iranian journal of pharmaceutical research
Published
2025-11-04
DOI
https://doi.org/10.5812/ijpr-164807
Primary Topic
Flavonoids in Medical Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Phenolic Compounds from Diarthron iranica: Enzymatic and in Silico Insights Into α-Amylase Inhibitory Activity

Morteza Sadeghi, Mustafa Ghanadian, Zeinab Yazdiniapour, Mehran Miroliaei et al.
Iranian journal of pharmaceutical research
Flavonoids in Medical Research
article

Phenolic Compounds from Diarthron iranica: Enzymatic and in Silico Insights Into α-Amylase Inhibitory Activity

Morteza Sadeghi, Mustafa Ghanadian, Zeinab Yazdiniapour, Mehran Miroliaei, Reza Gashavi, Tohid Khodabande, Hossein Biganeh
article en

Abstract

The phytochemical analysis carried out on the aerial parts of <i>D. iranica</i> yielded the identification and characterization of four phenolic compounds, including a methoxy apigenin glycoside (1), one bicoumarin (2), and two lignans (3-4). Molecular docking studies indicated that compound 1 exhibited superior inhibitory potential compared to compound 3, with stable interactions in the enzyme's binding site. In α-amylase inhibitory assays, these compounds displayed varying levels of activity, with compound 2 showing the highest potency (IC<sub>50</sub> = 0.71 mg/mL), followed by compounds 1 (IC<sub>50</sub> = 1.32 mg/mL) and 3 (IC<sub>50</sub> = 1.81 mg/mL). However, all were less effective than the reference compound luteolin (IC<sub>50</sub> = 0.63 mg/mL), which demonstrated superior efficacy.

Iranian journal of pharmaceutical researchVol. 24(1)
Isfahan University of Medical Sciences (IR), Islamic Azad University Sanandaj Branch (IR), University of Isfahan (IR)
Isfahan University of Medical Sciences
Openalex Percentile: Top 63%
Flavonoids in Medical Research
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