Isolation, characterization, antidiabetic and antityrosinase potentials of compounds isolated from Anabasis Articulata

• Anabasis articulata is a potential medicinal plant explored extensively for a broad range of biological spectrum. • Previously we documented the antidiabetic properties of its extracts and purified fractions. • Herein 4 potentially active compounds have been isolated and tested for their antidiabetic and antityrosinase potentials. • Out of the isolated compounds, compound 1 might be a drug candidate for treating for diabetes, hyperpigmentation disorders, and oxidative stress. Herein, we report the isolation, characterization, in silico evaluation and biological potentials of four compounds ( 1 - 4 ) isolated from A. Articulata. All compounds (isoleteolin ( 2 ), hyperoside ( 3 ) and quercitrin ( 4 )) demonstrated antioxidant properties; notably, quercetin ( 1 ) exhibited exceptional free-radical scavenging activity (87.75% DPPH and 85.75% ABTS at 1000 µg/mL) with an IC 50 value of 62 µg/mL, and 35 µg/mL, respectively against the tested radicals. The antidiabetic potential was revealed through the inhibition of α-glucosidase and α-amylase. All 4 compounds exhibited α-glucosidase activity (IC 50 =32-110 µg/mL) and α-amylase (30-59 µg/mL), among them quercetin showed maximum inhibition of 89.92% at 1000 µg/mL against α-glucosidase with an IC 50 value of 32 µg/mL, and 85.98% inhibition at 1000 µg/mL against α-amylase with an IC 50 value of 30 µg/mL. Next, along with quercetin, all compounds displayed dose-dependent behaviour in tyrosinase inhibition with IC 50 values ranging from 4.14-75.99 µM, whereas Lineweaver Burk and Dixon plots, displayed that quercetin with potent inhibition exhibited a competitive mode of inhibition. Further, in silico analyses validated the enzymatic binding affinity of quercetin with docking scores against α-glucosidase ( -5.37 kcal/mol), α-amylase (-5.82 kcal/mol), and tyrosinase (-5.37 kcal/mol), respectively. ADMET study revealed that quercetin possesses adequate water solubility, high bioavailability, and low toxicity. These results imply that quercetin has a great deal of promise as a treatment for diabetes, hyperpigmentation disorders, and oxidative stress.

Authors

Institutions

Publication Details

Journal
Applied Food Research
Published
2025-05-07
DOI
https://doi.org/10.1016/j.afres.2025.100949
Citations
2
Primary Topic
Natural Antidiabetic Agents Studies
Type
article
Field-Weighted Citation Impact
2.59
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Isolation, characterization, antidiabetic and antityrosinase potentials of compounds isolated from Anabasis Articulata

Haseena, Marwa Jan, Muhammad Esa, Muhammad Zahoor et al.
2 citations
Applied Food Research
Natural Antidiabetic Agents Studies
2.59
article

Isolation, characterization, antidiabetic and antityrosinase potentials of compounds isolated from Anabasis Articulata

Haseena, Marwa Jan, Muhammad Esa, Muhammad Zahoor, Fakhria A. Al‐Joufi, Mohsin Shahzad, Naila Gulfam, Abdul Bari Shah, Haroon Rashid
article en
2 citations

Abstract

• Anabasis articulata is a potential medicinal plant explored extensively for a broad range of biological spectrum. • Previously we documented the antidiabetic properties of its extracts and purified fractions. • Herein 4 potentially active compounds have been isolated and tested for their antidiabetic and antityrosinase potentials. • Out of the isolated compounds, compound 1 might be a drug candidate for treating for diabetes, hyperpigmentation disorders, and oxidative stress. Herein, we report the isolation, characterization, in silico evaluation and biological potentials of four compounds ( 1 - 4 ) isolated from A. Articulata. All compounds (isoleteolin ( 2 ), hyperoside ( 3 ) and quercitrin ( 4 )) demonstrated antioxidant properties; notably, quercetin ( 1 ) exhibited exceptional free-radical scavenging activity (87.75% DPPH and 85.75% ABTS at 1000 µg/mL) with an IC 50 value of 62 µg/mL, and 35 µg/mL, respectively against the tested radicals. The antidiabetic potential was revealed through the inhibition of α-glucosidase and α-amylase. All 4 compounds exhibited α-glucosidase activity (IC 50 =32-110 µg/mL) and α-amylase (30-59 µg/mL), among them quercetin showed maximum inhibition of 89.92% at 1000 µg/mL against α-glucosidase with an IC 50 value of 32 µg/mL, and 85.98% inhibition at 1000 µg/mL against α-amylase with an IC 50 value of 30 µg/mL. Next, along with quercetin, all compounds displayed dose-dependent behaviour in tyrosinase inhibition with IC 50 values ranging from 4.14-75.99 µM, whereas Lineweaver Burk and Dixon plots, displayed that quercetin with potent inhibition exhibited a competitive mode of inhibition. Further, in silico analyses validated the enzymatic binding affinity of quercetin with docking scores against α-glucosidase ( -5.37 kcal/mol), α-amylase (-5.82 kcal/mol), and tyrosinase (-5.37 kcal/mol), respectively. ADMET study revealed that quercetin possesses adequate water solubility, high bioavailability, and low toxicity. These results imply that quercetin has a great deal of promise as a treatment for diabetes, hyperpigmentation disorders, and oxidative stress.

Applied Food ResearchVol. 5(1)
Shaheed Benazir Bhutto Women University Peshawar (PK), Prince of Songkla University (TH), Universidade Federal de Pelotas (BR), Korea University (KR), Jouf University (SA), Government College University, Lahore (PK), University of Malakand (PK), Government College of Science (PK)
Zero hunger
Openalex Percentile: Top 10%
Natural Antidiabetic Agents Studies
2.59
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.