Novel pyrazole-based COX-2 inhibitors as potential anticancer agents: Design, synthesis, cytotoxic effect against resistant cancer cells, cell cycle arrest, apoptosis …

PA Halim, SMZ Sharkawi, MB Labib - Bioorganic Chemistry, 2023 - Elsevier
Novel differently substituted pyrazole derivatives were designed, synthesized and evaluated
for their anticancer activity. All compounds selectively inhibited COX-2 enzyme (IC 50 …

Design, synthesis and biological evaluation of novel diphenylthiazole-based cyclooxygenase inhibitors as potential anticancer agents

AH Abdelazeem, AM Gouda, HA Omar, MF Tolba - Bioorganic Chemistry, 2014 - Elsevier
Non-steroidal anti-inflammatory drugs (NSAIDs) are among the most widely used
medications as analgesics and antipyretics. Currently, there is a growing interest in their …

Biological evaluation and molecular docking studies of dimethylpyridine derivatives

P Świątek, K Gębczak, T Gębarowski, R Urniaz - Molecules, 2019 - mdpi.com
Cyclooxygenase inhibitors as anti-inflammatory agents can be used in chemoprevention.
Many in vitro and in vivo studies on human and animal models have explained the …

Combined Effects of Cyclooxygenase-1 and Cyclooxygenase-2 Selective Inhibitors on Ovarian Carcinoma in Vivo

W Li, J Wang, HR Jiang, XL Xu, J Zhang… - International journal of …, 2011 - mdpi.com
The present study was designed to investigate the combined effects of cyclooxygenase
(COX)-1 and COX-2 selective inhibitors on human ovarian SKOV-3 carcinoma cells …

Natural product inhibitors of cyclooxygenase (COX) enzyme: A review on current status and future perspectives

GG Ambati, SM Jachak - Current Medicinal Chemistry, 2021 - ingentaconnect.com
Background: Several clinically used COX-1 and COX-2 inhibitor drugs were reported to
possess severe side effects like GI ulcers and cardiovascular disturbances, respectively …

New imidazolone derivatives comprising a benzoate or sulfonamide moiety as anti-inflammatory and antibacterial inhibitors: Design, synthesis, selective COX-2 …

NH Metwally, MS Mohamed - Bioorganic Chemistry, 2020 - Elsevier
Abstract New imidazol-5-one derivatives 12a, b and 12e, f, 14a, b and 16a, b were
synthesized and screened for their in vivo anti-inflammatory activity using a standard acute …

Aspisol inhibits tumor growth and induces apoptosis in breast cancer

XG Zhu, L Tao, ZR Mei, HP Wu… - Experimental …, 2008 - dspace.nbuv.gov.ua
Nonsteroidal anti-inflammatory drugs inhibit cell proliferation and induce apoptosis in
various cancer cell lines, which is considered to be an important mechanism for their anti …

From COX-2 inhibitor nimesulide to potent anti-cancer agent: synthesis, in vitro, in vivo and pharmacokinetic evaluation

B Zhong, X Cai, S Chennamaneni, X Yi, L Liu… - European journal of …, 2012 - Elsevier
Cyclooxygenase-2 (COX-2) inhibitor nimesulide inhibits the proliferation of various types of
cancer cells mainly via COX-2 independent mechanisms, which makes it a good lead …

Discovery of novel 1, 3-diaryl pyrazolyl ester derivatives as COX-2 inhibitory candidates with anti-tumor effect

YS Yang, RJ Man, JF Xu, CY Wang, X Wang… - Journal of Molecular …, 2023 - Elsevier
Herein, a novel series of 1, 3-diaryl pyrazolyl ester derivatives were synthesized and
evaluated as potential COX-2 inhibitory candidates with anti-tumor effect. Among the four …

Synthesis, anti-inflammatory, ulcerogenic and cyclooxygenase activities of indenopyrimidine derivatives

SS Undare, NJ Valekar, AA Patravale… - Bioorganic & Medicinal …, 2016 - Elsevier
Objective of the present work was to evaluate the anti-inflammatory, ulcerogenicity and
cyclooxygenase activity of indenopyrimidine derivatives. Anti-inflammatory activity of the …