NSAIDs between past and present; a long journey towards an ideal COX-2 inhibitor lead

NA Khalil, EM Ahmed, T Tharwat, Z Mahmoud - RSC advances, 2024 - pubs.rsc.org
Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most abundantly used classes
among therapeutic agents in medicine. NSAIDs inhibit the enzyme cyclooxygenase (COX) …

N-Acylhydrazone Pharmacophore's Analgesic and Anti-inflammatory Profile: Recent Advancements during the Past Ten Years

AE Kassab - Current Pharmaceutical Design, 2024 - benthamdirect.com
Due to its important biological and pharmacological properties, in the field of medicinal
chemistry and drug discovery, the N-acylhydrazone motif has shown to be extremely …

[HTML][HTML] Synthesis, antibacterial evaluation, in silico ADMET and molecular docking studies of new N-acylhydrazone derivatives from acridone

M Aarjane, A Aouidate, S Slassi, A Amine - Arabian Journal of Chemistry, 2020 - Elsevier
Novel N-acylhydrazone derivatives from acridone have been synthesized by condensation
of acridone acetohydrazide and various aldehyde. The novel acylhydrazones were tested …

Synthesis of 3‐hydroxy‐2‐naphthohydrazide‐based hydrazones and their implications in diabetic management via in vitro and in silico approaches

M Tasleem, S Ullah, SA Halim, I Urooj… - Archiv der …, 2024 - Wiley Online Library
Diabetes mellitus (DM) has prevailed as a chronic health condition and has become a
serious global health issue due to its numerous consequences and high prevalence. We …

Biological evaluation of isoniazid derivatives as an anticancer class

FAR Rodrigues, ACA Oliveira… - Scientia …, 2013 - pmc.ncbi.nlm.nih.gov
A series of thirty-two isoniazid derivatives have been evaluated for their activity against four
human cancer cell lines with potent cytotoxicity (IC50 ranging from 0.61 to 3.36 μg/mL). The …

Synthesis and biological evaluation of new nicotinate derivatives as potential anti-inflammatory agents targeting COX-2 enzyme

Y El-Dash, NA Khalil, EM Ahmed, MSA Hassan - Bioorganic Chemistry, 2021 - Elsevier
Two novel series derived from nicotinic acid were synthesized and evaluated for their
inhibitory activity against cyclooxygenases COX-1 and COX-2, and their selectivity indices …

Synthesis and evaluation of anti-inflammatory and analgesic activities of new 1, 2, 4-triazole derivatives

F Ahmadi, M Rezayan Ghayahbashi… - Medicinal …, 2015 - ingentaconnect.com
In this study, the synthesis, anti-inflammatory and analgesic activities of eight new 5-thioalkyl-
1, 3-diaryl-1, 2, 4-triazole derivatives were reported. For the anti-inflammatory study, the …

[PDF][PDF] Xanthenone-based hydrazones as potent α-glucosidase inhibitors: Synthesis, solid state self-assembly and in silico studies

SU Khan, A Ashraf, M Ashraf, M Rafiq… - Bioorganic …, 2019 - academia.edu
Xanthenone based hydrazone derivatives (5a–n) have been synthesized as potential α-
glucosidase inhibitors. All synthesized compounds (5a–n) are characterized by their FTIR …

Iridium-catalyzed sp3 C–H Alkylation of 3-Carbonyl-2-(alkylamino)pyridines with Alkenes

M Nagai, M Nagamoto, T Nishimura… - Chemistry …, 2017 - academic.oup.com
Iridium-catalyzed C–H alkylation of 3-carbonyl-2-(alkylamino) pyridines via secondary sp3 C–
H activation adjacent to the nitrogen atom, with terminal alkenes proceeded to give the …

New tilomisole-based benzimidazothiazole derivatives as anti-inflammatory agents: Synthesis, in vivo, in vitro evaluation, and in silico studies

SA Darwish, MM El-Kerdawy, AR Elsheakh… - Bioorganic …, 2022 - Elsevier
New tilomisole-based benzimidazothiazole derivatives were designed and synthesized in
this work. Their anti-inflammatory activity was assessed through the in vivo carrageenan rat …