Eicosanoids in inflammation: biosynthesis, pharmacology, and therapeutic frontiers

SP Khanapure, DS Garvey, DR Janero… - Current topics in …, 2007 - ingentaconnect.com
In mammalian cells, eicosanoid biosynthesis is usually initiated by the activation of
phospholipase A2 and the release of arachidonic acid (AA) from membrane phospholipids …

[HTML][HTML] Role of non-steroidal anti-inflammatory drugs on intestinal permeability and nonalcoholic fatty liver disease

E Utzeri, P Usai - World journal of gastroenterology, 2017 - ncbi.nlm.nih.gov
The use of non-steroidal anti-inflammatory drugs (NSAIDs) is widespread worldwide thanks
to their analgesic, anti-inflammatory and antipyretic effects. However, even more attention is …

[HTML][HTML] Cyanidin-3-glucoside, a natural product derived from blackberry, exhibits chemopreventive and chemotherapeutic activity

M Ding, R Feng, SY Wang, L Bowman, Y Lu… - Journal of Biological …, 2006 - ASBMB
Epidemiological data suggest that consumption of fruits and vegetables has been
associated with a lower incidence of cancer. Cyanidin-3-glucoside (C3G), a compound …

2-(2-Arylphenyl) benzoxazole as a novel anti-inflammatory scaffold: synthesis and biological evaluation

K Seth, SK Garg, R Kumar, P Purohit… - ACS medicinal …, 2014 - ACS Publications
The 2-(2-arylphenyl) benzoxazole moiety has been found to be a new and selective ligand
for the enzyme cyclooxygenase-2 (COX-2). The 2-(2-arylphenyl) benzoxazoles 3a–m have …

Sulindac selectively inhibits colon tumor cell growth by activating the cGMP/PKG pathway to suppress Wnt/β-catenin signaling

N Li, Y Xi, HN Tinsley, E Gurpinar, BD Gary, B Zhu… - Molecular cancer …, 2013 - AACR
Nonsteroidal anti-inflammatory drugs (NSAID) display promising antineoplastic activity for
colorectal and other cancers, but toxicity from COX inhibition limits their long-term use for …

Coumarin sulfonamides derivatives as potent and selective COX-2 inhibitors with efficacy in suppressing cancer proliferation and metastasis

XY Lu, ZC Wang, SZ Ren, FQ Shen, RJ Man… - Bioorganic & medicinal …, 2016 - Elsevier
Cyclooxygenase-2 is frequently overexpression in malignant tumors and the product PGE 2
promotes cancer cell progression and metastasis. We designed novel series of coumarin …

Isatins inhibit cyclooxygenase-2 and inducible nitric oxide synthase in a mouse macrophage cell line

ME Matheus, F de Almeida Violante, SJ Garden… - European Journal of …, 2007 - Elsevier
Isatin is a versatile compound with a diversity of effects. We designed to investigate the
inhibitory effect of isatin derivatives on lipopolysaccharide/interferon-γ-induced expression …

Celecoxib analogs that lack COX-2 inhibitory function: preclinical development of novel anticancer drugs

AH Schönthal, TC Chen, FM Hofman… - Expert opinion on …, 2008 - Taylor & Francis
Celecoxib is an NSAID that was developed as a selective inhibitor of COX-2 and approved
by the FDA for the treatment of various forms of arthritis and the management of acute or …

Cyclooxygenase‐2 expression is critical for chronic UV‐induced murine skin carcinogenesis

SM Fischer, A Pavone, C Mikulec… - … in cooperation with …, 2007 - Wiley Online Library
While it has been established that both the constitutive and inducible forms of
cyclooxygenase (COX‐1 and COX‐2, respectively) play important roles in chemical initiation …

The dichotomous role of H2S in cancer cell biology? Deja vu all over again

K Kashfi - Biochemical pharmacology, 2018 - Elsevier
Nitric oxide (NO) a gaseous free radical is one of the ten smallest molecules found in nature,
while hydrogen sulfide (H 2 S) is a gas that bears the pungent smell of rotten eggs. Both are …