Unknown

Dataset Information

0

Exploring the Synergistic Anticancer Potential of Benzofuran-Oxadiazoles and Triazoles: Improved Ultrasound- and Microwave-Assisted Synthesis, Molecular Docking, Hemolytic, Thrombolytic and Anticancer Evaluation of Furan-Based Molecules.


ABSTRACT: Ultrasound- and microwave-assisted green synthetic strategies were applied to furnish benzofuran-oxadiazole 5a-g and benzofuran-triazole 7a-h derivatives in good to excellent yields (60-96%), in comparison with conventional methods (36-80% yield). These synthesized derivatives were screened for hemolysis, thrombolysis and anticancer therapeutic potential against an A549 lung cancer cell line using an MTT assay. Derivatives 7b (0.1%) and 5e (0.5%) showed the least toxicity against RBCs. Hybrid 7f showed excellent thrombolysis activity (61.4%) when compared against reference ABTS. The highest anticancer activity was displayed by the 5d structural hybridwith cell viability 27.49 ± 1.90 and IC50 6.3 ± 0.7 μM values, which were considerably lower than the reference drug crizotinib (IC50 8.54 ± 0.84 μM). Conformational analysis revealed the spatial arrangement of compound 5d, which demonstrated its significant potency in comparison with crizotinib; therefore, scaffold 5d would be a promising anticancer agent on the basis of cytotoxicity studies, as well as in silico modeling studies.

SUBMITTER: Irfan A 

PROVIDER: S-EPMC8838991 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Exploring the Synergistic Anticancer Potential of Benzofuran-Oxadiazoles and Triazoles: Improved Ultrasound- and Microwave-Assisted Synthesis, Molecular Docking, Hemolytic, Thrombolytic and Anticancer Evaluation of Furan-Based Molecules.

Irfan Ali A   Faiz Sadia S   Rasul Azhar A   Zafar Rehman R   Zahoor Ameer Fawad AF   Kotwica-Mojzych Katarzyna K   Mojzych Mariusz M  

Molecules (Basel, Switzerland) 20220202 3


Ultrasound- and microwave-assisted green synthetic strategies were applied to furnish benzofuran-oxadiazole <b>5a</b>-<b>g</b> and benzofuran-triazole <b>7a</b>-<b>h</b> derivatives in good to excellent yields (60-96%), in comparison with conventional methods (36-80% yield). These synthesized derivatives were screened for hemolysis, thrombolysis and anticancer therapeutic potential against an A549 lung cancer cell line using an MTT assay. Derivatives <b>7b</b> (0.1%) and <b>5e</b> (0.5%) showed  ...[more]

Similar Datasets

| S-EPMC5271595 | biostudies-literature
| S-EPMC9050871 | biostudies-literature
| S-EPMC10669698 | biostudies-literature
| S-EPMC9369641 | biostudies-literature
| S-EPMC6072493 | biostudies-literature
| S-EPMC10778652 | biostudies-literature
| S-EPMC10480608 | biostudies-literature
| S-EPMC10925991 | biostudies-literature
2022-03-30 | GSE194209 | GEO
| S-EPMC9041371 | biostudies-literature