4-Thiazolidinone-bearing hybrid molecules in anticancer drug design
P Roszczenko, S Holota, OK Szewczyk… - International Journal of …, 2022 - mdpi.com
Oncological diseases have currently reached an epidemic scale, especially in industrialized
countries. Such a situation has prompted complex studies in medicinal chemistry focused on …
countries. Such a situation has prompted complex studies in medicinal chemistry focused on …
The bioactivity of thiazolidin-4-ones: A short review of the most recent studies
D Mech, A Kurowska, N Trotsko - International Journal of Molecular …, 2021 - mdpi.com
Thiazolidin-4-ones is an important heterocyclic ring system of a pharmacophore and a
privileged scaffold in medicinal chemistry. This review is focused on the latest scientific …
privileged scaffold in medicinal chemistry. This review is focused on the latest scientific …
A Review of the Recent Developments of Molecular Hybrids Targeting Tubulin Polymerization
O Ebenezer, M Shapi, JA Tuszynski - International Journal of Molecular …, 2022 - mdpi.com
Microtubules are cylindrical protein polymers formed from α β-tubulin heterodimers in the
cytoplasm of eukaryotic cells. Microtubule disturbance may cause cell cycle arrest in the …
cytoplasm of eukaryotic cells. Microtubule disturbance may cause cell cycle arrest in the …
Potential Fluorinated Anti‐MRSA Thiazolidinone Derivatives with Antibacterial, Antitubercular Activity and Molecular Docking Studies
V Kumar, P Shetty, A HS, S Chandra K… - Chemistry & …, 2022 - Wiley Online Library
MRSA infection is one of the alarming diseases in the current scenario. Identifying newer
molecules to treat MRSA infection is of urgent need. In the present study, we have designed …
molecules to treat MRSA infection is of urgent need. In the present study, we have designed …
An alternative technique for cyclization synthesis, in vitro anti-esophageal cancer evaluation, and molecular docking of novel thiazolidin-4-one derivatives
In this work, two novel series of thiazolidin-4-one derivatives (9a–e and 10a–e) constituting
ten compounds were synthesized under batch and ultrasound irradiation. It is found that the …
ten compounds were synthesized under batch and ultrasound irradiation. It is found that the …
Synthesis, anticancer evaluation and in silico studies of novel N‐substituted arylidenethiazolidine‐2, 4‐dione derivatives as adenosine monophosphate‐activated …
SR Chothani, CA Chamakiya, RJ Joshi… - Journal of …, 2024 - Wiley Online Library
Abstract Design and development of AMP‐activated protein kinase (AMPK) activator
emerged as a potential therapeutic approach for various types of cancers. In this context …
emerged as a potential therapeutic approach for various types of cancers. In this context …
[HTML][HTML] Methyl 6, 7-Difluoro-2-[(4-fluorobenzyl) sulfanyl]-4-hydroxyquinoline-3-carboxylate
VA Potapov, IA Novokshonova, MV Musalov… - Molbank, 2024 - mdpi.com
A convenient synthesis of a novel fluoroquinolone precursor, methyl 6, 7-difluoro-2-[(4-
fluorobenzyl) sulfanyl]-4-hydroxyquinoline-3-carboxylate, at a 78% yield starting from 3, 4 …
fluorobenzyl) sulfanyl]-4-hydroxyquinoline-3-carboxylate, at a 78% yield starting from 3, 4 …
[PDF][PDF] Proton tautomerism and stereoisomerism in 1, 3-thiazolidinone derivatives
A Pyrih - 2023 - repozytorium.amu.edu.pl
The thesis presents the synthesis and structural analysis of a series of hybrid 1H-pyrazolin/
thiazolidinones as well as of 5-ylidene derivatives of 4-phenylamino-1, 3-thiazol-2 (5H)-ones …
thiazolidinones as well as of 5-ylidene derivatives of 4-phenylamino-1, 3-thiazol-2 (5H)-ones …