[PDF][PDF] Evolution of nonsteroidal anti-inflammatory drugs (NSAIDs): cyclooxygenase (COX) inhibition and beyond

P Rao, EE Knaus - Journal of pharmacy & pharmaceutical …, 2008 - frontierspartnerships.org
Purpose. NSAIDs constitute an important class of drugs with therapeutic applications that
have spanned several centuries. Treatment of inflammatory conditions such as rheumatoid …

Safer anti-inflammatory therapy through dual COX-2/5-LOX inhibitors: A structure-based approach

SL Manju, KR Ethiraj, G Elias - European Journal of Pharmaceutical …, 2018 - Elsevier
Inflammatory mediators of the arachidonic acid cascade from cyclooxygenase (COX) and
lipoxygenase (LOX) pathways are primarily responsible for many diseases in human beings …

In situ click chemistry generation of cyclooxygenase-2 inhibitors

A Bhardwaj, J Kaur, M Wuest, F Wuest - Nature communications, 2017 - nature.com
Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and
overexpression of this enzyme is also associated with several cancers and …

Sulfonamides: a patent review (2008–2012)

F Carta, A Scozzafava, CT Supuran - Expert opinion on therapeutic …, 2012 - Taylor & Francis
Introduction: The primary sulfonamide moiety is present in many clinically used drugs, such
as diuretics (furosemide, indapamide, chlorthalidone, thiazides); carbonic anhydrase (CA) …

Multi-and poly-pharmacology of carbonic anhydrase inhibitors

CT Supuran - Pharmacological reviews, 2024 - Elsevier
Eight genetically distinct families of the enzyme carbonic anhydrase (CA, EC 4.2. 1.1) were
described in organisms allover the phylogenetic tree. They catalyze the hydration of CO 2 to …

Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents

M Amir, H Kumar, SA Khan - Bioorganic & medicinal chemistry letters, 2008 - Elsevier
A series of 3-(4-biphenyl)-5-substituted phenyl-2-pyrazolines (2a–h) and 1-benzoyl-3-(4-
biphenyl)-5-substituted phenyl-2-pyrazolines (3a–h) were synthesized by condensation of …

1, 3, 4-Oxadiazole/thiadiazole and 1, 2, 4-triazole derivatives of biphenyl-4-yloxy acetic acid: synthesis and preliminary evaluation of biological properties

H Kumar, SA Javed, SA Khan, M Amir - European journal of medicinal …, 2008 - Elsevier
A series of 1, 3, 4-oxadiazole/thiadiazole and 1, 2, 4-triazole derivatives of biphenyl-4-yloxy
acetic acid were synthesized in order to obtain new compounds with potential anti …

Preparation of 5-aryl-3-alkylthio-l, 2, 4-triazoles and corresponding sulfones with antiinflammatory–analgesic activity

B Tozkoparan, E Küpeli, E Yeşilada, M Ertan - Bioorganic & medicinal …, 2007 - Elsevier
In this study, a series of 5-aryl-3-alkylthio-1, 2, 4-triazoles and corresponding sulfones were
prepared with the objective of develo** better analgesic–antiinflammatory compounds …

Design and synthesis of ibuprofen-quinoline conjugates as potential anti-inflammatory and analgesic drug candidates

AM Ghanim, AS Girgis, BM Kariuki, N Samir, MF Said… - Bioorganic …, 2022 - Elsevier
A new set of ibuprofen-quinoline conjugates comprising quinolinyl heterocycle and
ibuprofen moieties linked by an alkyl chain were synthesized in good yields utilizing an …

Impeding the interaction between Nur77 and p38 reduces LPS-induced inflammation

L Li, Y Liu, H Chen, F Li, J Wu, H Zhang, J He… - Nature chemical …, 2015 - nature.com
Sepsis, a hyperinflammatory response that can result in multiple organ dysfunctions, is a
leading cause of mortality from infection. Here, we show that orphan nuclear receptor Nur77 …