[HTML][HTML] Selective COX-2 inhibitors: a review of their structure-activity relationships

A Zarghi, S Arfaei - Iranian journal of pharmaceutical research …, 2011 - ncbi.nlm.nih.gov
Non-steroidal anti-inflammatory drugs (NSAIDs) are the competitive inhibitors of
cyclooxygenase (COX), the enzyme which mediates the bioconversion of arachidonic acid …

Progress in COX-2 inhibitors: a journey so far

AK Chakraborti, SK Garg, R Kumar… - Current medicinal …, 2010 - ingentaconnect.com
The non-steroidal anti-inflammatory drugs (NSAIDs) are diverse group of compounds used
for the treatment of inflammation, since the introduction of acetylsalicylic acid in 1899 …

Supported protic acid-catalyzed synthesis of 2, 3-disubstituted thiazolidin-4-ones: enhancement of the catalytic potential of protic acid by adsorption on solid supports

D Kumar, M Sonawane, B Pujala, VK Jain, S Bhagat… - Green chemistry, 2013 - pubs.rsc.org
The catalytic potential of various protic acids has been assessed for the one pot tandem
condensation–cyclisation reaction involving an aldehyde, an amine, and thioglycolic acid to …

Design, synthesis and biological screening of new 4-thiazolidinone derivatives with promising COX-2 selectivity, anti-inflammatory activity and gastric safety profile

KRA Abdellatif, MA Abdelgawad, HAH Elshemy… - Bioorganic …, 2016 - Elsevier
Two series of new thiazolidin-4-one derivatives 4a–c and 8a–e were designed and
prepared. All the synthesized compounds were evaluated for their in vitro COX-2 selectivity …

Discovery and optimization of 2, 3-diaryl-1, 3-thiazolidin-4-one-based derivatives as potent and selective cytotoxic agents with anti-inflammatory activity

AM Shawky, FA Almalki, AN Abdalla… - European Journal of …, 2023 - Elsevier
Several studies have indicated the potential therapeutic outcomes of combining selective
COX-2 inhibitors with tubulin-targeting anticancer agents. In the current study, a novel series …

3-Methyl-2-phenyl-1-substituted-indole derivatives as indomethacin analogs: design, synthesis and biological evaluation as potential anti-inflammatory and analgesic …

KRA Abdellatif, PF Lamie, HA Omar - Journal of Enzyme Inhibition …, 2016 - Taylor & Francis
In a new group of 3-methyl-2-phenyl-1-substituted-indole derivatives (10a–f), the
indomethacin analogs were prepared via the Fisher indole synthesis reaction of …

Dual COX-2/15-LOX inhibitors: A new avenue in the prevention of cancer

A Aliabadi, E Khanniri, M Mahboubi-Rabbani… - European journal of …, 2023 - Elsevier
Abstract Dual cyclooxygenase 2/15-lipoxygenase inhibitors constitute a valuable alternative
to classical non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 …

Ionic liquid mediated and promoted eco-friendly preparation of thiazolidinone and pyrimidine nucleoside–thiazolidinone hybrids and their antiparasitic activities

X Zhang, X Li, D Li, G Qu, J Wang, PM Loiseau… - Bioorganic & medicinal …, 2009 - Elsevier
Without any catalyst, 2, 3-disubstituted-1, 3-thiazolidin-4-one derivatives were synthesized
efficiently via the three-component reaction of aldehyde, amine and mercaptoacetic acid in …

Molecular modeling, synthesis and screening of some new 4-thiazolidinone derivatives with promising selective COX-2 inhibitory activity

O Unsal-Tan, K Ozadali, K Piskin, A Balkan - European journal of medicinal …, 2012 - Elsevier
In order to develop new selective cyclooxygenase-2 inhibitors, a series of novel 2-aryl-3-(4-
sulfamoyl/methylsulfonylphenylamino)-4-thiazolidinones were designed. Molecular …

Recent advances in synthetic strategies and SAR of thiazolidin-4-one containing molecules in cancer therapeutics

A Sharma, D Sharma, N Saini, SV Sharma… - Cancer and Metastasis …, 2023 - Springer
Cancer is one of the life-threatening diseases accountable for millions of demises globally.
The inadequate effectiveness of the existing chemotherapy and its harmful effects has …