Ultrasound-assisted synthesis of α-aminophosphonates using nano ZnO catalyst: evaluation of their anti-diabetic activity

A more efficient and environmentally friendly way of synthesizing -aminophosphonates is achieved by employing nano-ZnO to catalyze the Kabachnik-Fields reaction under ultrasonication within a solvent-free environment.Before synthesis, molecular docking and in silico ADME analysis were used to assess each molecule's drug-like characteristics and ability to inhibit -amylase and -glucosidase.The newly synthesized compounds' in vitro inhibitory effects on -amylase and -glucosidase were also evaluated, and their structure was confirmed using spectroscopic investigation.The target enzyme was effectively inhibited by most of the substances.In comparison to the reference drug, acarbose (IC50, 106.50.6 g/mL), compounds 4d (IC50, 102.20.3 g/mL), 4h (IC50, 102.90.4 g/mL), which contained a 2H-1,3-benzodioxol-5-yl moiety, and 4i (IC50, 103.90.5 g/mL) showed the strongest inhibitory activity.The enzyme inhibition of the remaining compounds ranged from moderate to good.

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Publication Details

Journal
Organic Communications
Published
2024-12-30
DOI
https://doi.org/10.25135/acg.oc.180.2412.3384
Primary Topic
Organophosphorus compounds synthesis
Type
article
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article

Ultrasound-assisted synthesis of α-aminophosphonates using nano ZnO catalyst: evaluation of their anti-diabetic activity

V. Lakshmi, Meson Haji Basha, Mohan Seelam, K. Kiran Kumar et al.
Organic Communications
Organophosphorus compounds synthesis
article

Ultrasound-assisted synthesis of α-aminophosphonates using nano ZnO catalyst: evaluation of their anti-diabetic activity

V. Lakshmi, Meson Haji Basha, Mohan Seelam, K. Kiran Kumar, C. Gladis Raja Malar, Chennamsetty Subramanyam, K. Prasada Rao
article en

Abstract

A more efficient and environmentally friendly way of synthesizing -aminophosphonates is achieved by employing nano-ZnO to catalyze the Kabachnik-Fields reaction under ultrasonication within a solvent-free environment.Before synthesis, molecular docking and in silico ADME analysis were used to assess each molecule's drug-like characteristics and ability to inhibit -amylase and -glucosidase.The newly synthesized compounds' in vitro inhibitory effects on -amylase and -glucosidase were also evaluated, and their structure was confirmed using spectroscopic investigation.The target enzyme was effectively inhibited by most of the substances.In comparison to the reference drug, acarbose (IC50, 106.50.6 g/mL), compounds 4d (IC50, 102.20.3 g/mL), 4h (IC50, 102.90.4 g/mL), which contained a 2H-1,3-benzodioxol-5-yl moiety, and 4i (IC50, 103.90.5 g/mL) showed the strongest inhibitory activity.The enzyme inhibition of the remaining compounds ranged from moderate to good.

Organic Communications(4)
Vel Tech Rangarajan Dr. Sagunthala R&D Institute of Science and Technology (IN), Acharya Nagarjuna University (IN), St. Theresa’s Multi-Speciality Hospital (IN)
Openalex Percentile: Top 82%
Organophosphorus compounds synthesis
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