Synthetic approaches, functionalization and therapeutic potential of quinazoline and quinazolinone skeletons: The advances continue

I Khan, A Ibrar, W Ahmed, A Saeed - European journal of medicinal …, 2015 - Elsevier
The presence of N-heterocycles as an essential structural motif in a variety of biologically
active substances has stimulated the development of new strategies and technologies for …

An overview of triazoloquinazolines: Pharmacological significance and recent developments

HA Abuelizz, R Al-Salahi - Bioorganic Chemistry, 2021 - Elsevier
Nitrogen heterocyclic rings have participated to constitute most of the drugs and several
pharmacologically related compounds. The existence of such hetero atoms/groups in …

[HTML][HTML] Synthesis and anticancer activity of new quinazoline derivatives

HA Abuelizz, M Marzouk, H Ghabbour… - Saudi Pharmaceutical …, 2017 - Elsevier
In this study, a new series of quinazoline derivatives (3–26) was synthesized and
characterized via physicochemical and spectral means. Treatment of 2-amino-5 …

A DFT Study and Hirshfeld Surface Analysis of the Molecular Structures, Radical Scavenging Abilities and ADMET Properties of 2-Methylthio (methylsulfonyl)-[1, 2, 4] …

AH Bakheit, HA Abuelizz, R Al-Salahi - Crystals, 2023 - mdpi.com
Optimisation at B3LYP/6-311G (d, p) was used in a DFT study of the characteristics of 2-
methylthio (methylsulfonyl)-triazoloquinazolines (1, 2). The design-critical role of …

Triazoloquinazolines as a new class of potent α-glucosidase inhibitors: in vitro evaluation and docking study

HA Abuelizz, EH Anouar, R Ahmad, NIIN Azman… - PLoS …, 2019 - journals.plos.org
Previously, we synthesized triazoloquinazolines 1–14 and characterized their structure. In
this study, we aimed to evaluate the in vitro activity of the targets 1–14 as α-glucosidase …

1, 2, 4-Triazolo-quinazolinones as Effective Antifoulants: Molecular Design, Synthesis, and Biological Evaluation

S Gudala, M Dong, X Lin, R Liu, A Vinothkanna, A Jha… - Langmuir, 2024 - ACS Publications
A series of 1, 2, 4-triazolo-quinazolinones and 1, 2-benzisothiazolone derivatives (S1–S12)
were successfully synthesized as environmentally friendly alternatives to copper-based …

Biological Evaluation of 4-(1H-triazol-1-yl) benzoic Acid Hybrids as Antioxidant Agents: In Vitro Screening and DFT Study

HA Abuelizz, HAA Taie, AH Bakheit, M Marzouk… - Applied Sciences, 2021 - mdpi.com
Fourteen triazole benzoic acid hybrids were previously characterized. This work aimed to
screen their in vitro antioxidant activity using different assays, ie, DPPH (1, 1-diphenyl-1 …

Screening and Evaluation of Antioxidant Activity of Some 1,2,4-triazolo[1,5-a]quinazoline Derivatives

R Al-Salahi, EH Anouar, M Marzouk… - Future Medicinal …, 2018 - Taylor & Francis
Aim: The present study was carried out to assess a new series of triazoloquinazolines 1–40
for their antioxidant activities using 1, 1-diphenyl-2-picryl hydrazyl radical scavenging, ferric …

[PDF][PDF] Aj csian ournalof hemistry aj csian ournalof hemistry

VK SHARMA, A BARDE, S RATTAN - Asian Journal of Chemistry, 2020 - academia.edu
Novel thiazolidine-2, 4-dione (TZD) based pyrimidine derivatives have been synthesized by
Knoevenagel condensation reaction between thiazolidine-2, 4-dione and amino pyrimidinyl …

Synthesis, biological activity and molecular docking of new tricyclic series as α-glucosidase inhibitors

HA Abuelizz, NANI Iwana, R Ahmad, EH Anouar… - BMC chemistry, 2019 - Springer
Diabetes is an emerging metabolic disorder. α-Glucosidase inhibitors, such as acarbose,
delay the hydrolysis of carbohydrates by interfering with the digestive enzymes. This action …