4-Thiazolidinones: the advances continue…

AC Tripathi, SJ Gupta, GN Fatima, PK Sonar… - European Journal of …, 2014 - Elsevier
The diversity in the biological response of 4-thiazolidinones has attracted the attention of
many researchers to explore this framework for its potential. It is, therefore, of prime …

5-Ene-4-thiazolidinones–An efficient tool in medicinal chemistry

D Kaminskyy, A Kryshchyshyn, R Lesyk - European journal of medicinal …, 2017 - Elsevier
The presented review is an attempt to summarize a huge volume of data on 5-ene-4-
thiazolidinones being a widely studied class of small molecules used in modern organic and …

Synthesis of novel diflunisal hydrazide–hydrazones as anti-hepatitis C virus agents and hepatocellular carcinoma inhibitors

S Şenkardeş, N Kaushik-Basu, I Durmaz… - European journal of …, 2016 - Elsevier
Highlights•We synthesized new diflunisal hydrazide–hydrazones.•We investigated their
activity against hepatitis C virus (HCV).•Some compounds exhibited strong inhibition against …

Structure-based virtual screening, synthesis and SAR of novel inhibitors of hepatitis C virus NS5B polymerase

TT Talele, P Arora, SS Kulkarni, MR Patel… - Bioorganic & medicinal …, 2010 - Elsevier
Hepatitis C virus (HCV) NS5B polymerase is a key target for the development of therapeutic
agents aimed at the treatment of HCV infections. Here we report on the identification of novel …

2-Heteroarylimino-5-arylidene-4-thiazolidinones as a new class of non-nucleoside inhibitors of HCV NS5B polymerase

İ Küçükgüzel, G Satılmış, KR Gurukumar, A Basu… - European Journal of …, 2013 - Elsevier
Abstract Hepatitis C virus (HCV) NS5B polymerase is an important and attractive target for
the development of anti-HCV drugs. Here we report on the design, synthesis and evaluation …

[HTML][HTML] Synthesis and characterization of celecoxib derivatives as possible anti-inflammatory, analgesic, antioxidant, anticancer and anti-HCV agents

ŞG Küçükgüzel, İ Coşkun, S Aydın, G Aktay, Ş Gürsoy… - Molecules, 2013 - mdpi.com
A series of novel N-(3-substituted aryl/alkyl-4-oxo-1, 3-thiazolidin-2-ylidene)-4-[5-(4-
methylphenyl)-3-(trifluoromethyl)-1 H-pyrazol-1-yl] benzenesulfonamides 2a–e were …

Non-nucleoside inhibitors of the hepatitis C virus NS5B RNA-dependant RNA polymerase: 2-aryl-3-heteroaryl-1, 3-thiazolidin-4-one derivatives

RK Rawal, SB Katti, N Kaushik-Basu, P Arora… - Bioorganic & medicinal …, 2008 - Elsevier
Hepatitis C virus (HCV) NS5B RNA polymerase is crucial for replicating the HCV RNA
genome and is an attractive target for developing anti-HCV drugs. A novel series of 2, 3 …

Microwave assisted synthesis of some novel Flurbiprofen hydrazidehydrazones as anti-HCV NS5B and anticancer agents

S Aydın, N Kaushik-Basu, P Arora, A Basu… - Marmara …, 2013 - dergipark.org.tr
The synthesis of a new series of flurbiprofen hydrazide-hydrazones using
microwaveassisted reactions is described. Substituted aldehydes were condensed with …

Allosteric Inhibition of the Hepatitis C Virus NS5B Polymerase: In Silico Strategies for Drug Discovery and Development

ML Barreca, N Iraci, G Manfroni… - Future Medicinal …, 2011 - Taylor & Francis
Chronic infection by hepatitis C virus (HCV) often leads to severe liver disease including
cirrhosis, hepatocellular carcinoma and liver failure. Despite it being more than 20 years …

Novel 4‐thiazolidinones as non‐nucleoside inhibitors of hepatitis C virus NS5B RNA‐dependent RNA polymerase

G Çakır, İ Küçükgüzel, R Guhamazumder… - Archiv der …, 2015 - Wiley Online Library
In continuation of our efforts to develop new derivatives as hepatitis C virus (HCV) NS5B
inhibitors, we synthesized novel 5‐arylidene‐4‐thiazolidinones. The novel compounds 29 …