Rhodanine as a privileged scaffold in drug discovery

T Tomasic, LP Masic - Current Medicinal Chemistry, 2009 - ingentaconnect.com
Rhodanines, thiazolidine-2, 4-diones and pseudothiohydantoins have become a very
interesting class of heterocyclic compounds since the introduction of various glitazones and …

Therapeutic journey of 2, 4-thiazolidinediones as a versatile scaffold: An insight into structure activity relationship

MJ Naim, MJ Alam, S Ahmad, F Nawaz… - European journal of …, 2017 - Elsevier
Thiazolidinedione is an important heterocyclic ring system, a pharmacophore and a
privileged scaffold in medicinal chemistry; is a derivative of thiazolidine ring which came into …

GQ-16, a novel peroxisome proliferator-activated receptor γ (PPARγ) ligand, promotes insulin sensitization without weight gain

AA Amato, S Rajagopalan, JZ Lin, BM Carvalho… - Journal of Biological …, 2012 - ASBMB
The recent discovery that peroxisome proliferator-activated receptor γ (PPARγ) targeted anti-
diabetic drugs function by inhibiting Cdk5-mediated phosphorylation of the receptor has …

Acridine and its derivatives: a patent review (2009–2013)

B Zhang, X Li, B Li, C Gao, Y Jiang - Expert opinion on therapeutic …, 2014 - Taylor & Francis
Introduction: Acridine derivatives have been extensively explored as potential therapeutic
agents for the treatment of a number of diseases, such as cancer, Alzheimer's, and bacterial …

Synthesis and biological evaluation of thiazolidine-2, 4-dione-pyrazole conjugates as antidiabetic, anti-inflammatory and antioxidant agents

G Bansal, S Singh, V Monga, PV Thanikachalam… - Bioorganic …, 2019 - Elsevier
A series of fourteen novel thiazolidine-2, 4-dione derivatives clubbed with pyrazole moiety
were synthesized via four step reaction procedure. Reactions were monitored by thin layer …

[HTML][HTML] Synthesis and anti-inflammatory activity of new arylidene-thiazolidine-2, 4-diones as PPARγ ligands

CD Barros, AA Amato, TB de Oliveira… - Bioorganic & medicinal …, 2010 - Elsevier
Eight new 5-arylidene-3-benzyl-thiazolidine-2, 4-diones with halide groups on their benzyl
rings were synthesized and assayed in vivo to investigate their anti-inflammatory activities …

[HTML][HTML] In silico and in vitro insights into tyrosinase inhibitors with a 2-thioxooxazoline-4-one template

I Choi, Y Park, IY Ryu, HJ Jung, S Ullah, H Choi… - Computational and …, 2021 - Elsevier
The β-phenyl-α, β-unsaturated carbonyl (PUSC) scaffold confers tyrosinase inhibitory
activity, and in the present study, 16 (Z)-5-(substituted benzylidene)-3-phenyl-2 …

Synthesis and cytotoxic activity of new acridine-thiazolidine derivatives

FWA Barros, TG Silva, MG da Rocha Pitta… - Bioorganic & medicinal …, 2012 - Elsevier
Although their exact role in controlling tumour growth and apoptosis in humans remains
undefined, acridine and thiazolidine compounds have been shown to act as tumour …

Novel 4‐heteroaryl‐antipyrines as DPP‐IV inhibitors

SM Gomha, TMA Eldebss, MG Badrey… - Chemical Biology & …, 2015 - Wiley Online Library
Type 2 diabetes mellitus is a vast growing progressive disease that almost affects one
person among every twelve globally. Regardless the availability of wide variety of oral …

Synthesis, biological evaluation and molecular modeling studies of arylidene-thiazolidinediones with potential hypoglycemic and hypolipidemic activities

LFC da Costa Leite, RHV Mourão, MCA de Lima… - European journal of …, 2007 - Elsevier
New arylidene-thiazolidinediones (ATZDs) were synthesized and evaluated in the alloxan-
induced hyperglycemia mice model. The molecular target taken into consideration is the …