Carbonic anhydrase inhibition and the management of neuropathic pain

CT Supuran - Expert review of neurotherapeutics, 2016 - Taylor & Francis
Introduction: Neuropathic pain affects up to 8% of the population with few therapeutic
options for its management. No specific drugs are approved for its treatment. Areas covered …

Selective cyclooxygenase-2 inhibitors: A review of recent chemical scaffolds with promising anti-inflammatory and COX-2 inhibitory activities

NA Mohsin, M Irfan - Medicinal Chemistry Research, 2020 - Springer
Abstract Selective cyclooxygenase-2 (COX-2) inhibitors have exhibited notable medicinal
importance. In recent years, the discovery of new anti-inflammatory agents as selective COX …

A class of sulfonamide carbonic anhydrase inhibitors with neuropathic pain modulating effects

F Carta, LDC Mannelli, M Pinard, C Ghelardini… - Bioorganic & medicinal …, 2015 - Elsevier
A series of benzene sulfonamide carbonic anhydrase (CA, EC 4.2. 1.1) inhibitors which
incorporate lipophilic 4-alkoxy-and 4-aryloxy moieties, together with several derivatives of …

An operationally simple, one‐pot, convenient synthesis, and in vitro anti‐inflammatory activity of some new spirotriazolotriazine derivatives

AM El‐Saghier, SS Enaili, A Abdou… - Journal of …, 2024 - Wiley Online Library
The wide biological actions of triazolotriazine hybrids, benzene‐sulfonamide derivatives,
exhibit a good chance of displaying in vitro anti‐inflammatory effects. An operationally …

Discovery of novel nonsteroidal anti-inflammatory drugs and carbonic anhydrase inhibitors hybrids (NSAIDs–CAIs) for the management of rheumatoid arthritis

O Akgul, L Di Cesare Mannelli, D Vullo… - Journal of medicinal …, 2018 - ACS Publications
Herein we report the design as well as the synthesis of a new series of dual hybrid
compounds consisting of the therapeutically used nonsteroidal-anti-inflammatory drugs …

[HTML][HTML] Synthesis and biological evaluation studies of novel quinazolinone derivatives as antibacterial and anti-inflammatory agents

MF Zayed, MH Hassan - Saudi pharmaceutical journal, 2014 - Elsevier
Abstract Some novel 6, 8-diiodo-2-methyl-3-substituted-quinazolin-4 (3H)-ones bearing
sulfonamide derivatives (4–11) were synthesized in good yields and evaluated for their …

Dual cyclooxygenase and carbonic anhydrase inhibition by nonsteroidal anti-inflammatory drugs for the treatment of cancer

C De Monte, S Carradori, A Gentili… - Current Medicinal …, 2015 - ingentaconnect.com
Among the class of nonsteroidal anti-inflammatory drugs (NSAIDs), COX-2 inhibitors or
“coxibs” selectively inhibit the activity of the inducible isoform of cyclooxygenase. Moreover …

[HTML][HTML] Pathophysiological investigations, anxiolytic effects and interaction of a semisynthetic riparin with benzodiazepine receptors

ÉJF de Araújo, LM Rezende-Júnior, LKF Lima… - Biomedicine & …, 2018 - Elsevier
We have reported Riparin A as a promising antiparasitic molecule​​ against Leishmania
amazonensis promastigotes. This work evaluated the acute oral toxicity of Riparin A and its …

Methyl-linked pyrazoles: synthetic and medicinal perspective

T Sharma, J Singh, B Singh, R Kataria… - Mini Reviews in …, 2022 - ingentaconnect.com
Pyrazoles, an important and well-known class of the azole family, have been found to show
a large number of applications in various fields, especially medicinal chemistry. Pyrazole …

Endogenous opioid and cannabinoid mechanisms are involved in the analgesic effects of celecoxib in the central nervous system

RM Rezende, P Paiva-Lima, WGP Dos Reis… - Pharmacology, 2012 - karger.com
Abstract Background/Aims: In this study we analyzed the mechanisms underlying celecoxib-
induced analgesia in a model of inflammatory pain in rats, using the intracerebroventricular …