[HTML][HTML] Selective COX-2 inhibitors: a review of their structure-activity relationships

A Zarghi, S Arfaei - Iranian journal of pharmaceutical research …, 2011 - ncbi.nlm.nih.gov
Non-steroidal anti-inflammatory drugs (NSAIDs) are the competitive inhibitors of
cyclooxygenase (COX), the enzyme which mediates the bioconversion of arachidonic acid …

Biological importance of imidazole nucleus in the new millennium

B Narasimhan, D Sharma, P Kumar - Medicinal Chemistry Research, 2011 - Springer
Imidazole nucleus is a constituent of many bioactive heterocyclic compounds that are of
wide interest because of their diverse biological and clinical applications. This created …

Synthesis and evaluation of anti-tubercular and antibacterial activities of new 4-(2, 6-dichlorobenzyloxy) phenyl thiazole, oxazole and imidazole derivatives. Part 2

X Lu, X Liu, B Wan, SG Franzblau, L Chen… - European journal of …, 2012 - Elsevier
A series of substituted 4-(2, 6-dichlorobenzyloxy) phenyl thiazole, oxazole and imidazole
derivatives were synthesized. The derivatives were screened for in vitro anti-tubercular …

Progress in COX-2 inhibitors: a journey so far

AK Chakraborti, SK Garg, R Kumar… - Current medicinal …, 2010 - ingentaconnect.com
The non-steroidal anti-inflammatory drugs (NSAIDs) are diverse group of compounds used
for the treatment of inflammation, since the introduction of acetylsalicylic acid in 1899 …

[HTML][HTML] In vitro screening, homology modeling and molecular docking studies of some pyrazole and imidazole derivatives

F Abrigach, Y Rokni, A Takfaoui, M Khoutoul… - Biomedicine & …, 2018 - Elsevier
A series of synthesized compounds based on pyrazole and imidazole skeletons prepared by
palladium catalysts via a one-pot reaction was screened to determine their inhibitory …

The discovery and development of cyclooxygenase-2 inhibitors as potential anticancer therapies

M Vosooghi, M Amini - Expert opinion on drug discovery, 2014 - Taylor & Francis
Introduction: In the past, clinical studies had demonstrated that aspirin and NSAIDs reduce
the risk of colorectal cancer. After the discovery of selective prostaglandin-endoperoxide …

o-Iodoxybenzoic Acid Mediated Oxidative Desulfurization Initiated Domino Reactions for Synthesis of Azoles

PS Chaudhari, SP Pathare… - The Journal of organic …, 2012 - ACS Publications
A systematic exploration of thiophilic ability of o-iodoxybenzoic acid (IBX) for oxidative
desulfurization to trigger domino reactions leading to new methodologies for synthesis of …

Palladium-catalyzed four-component cascade carbonylative cyclization to access carbonyl-bridged bisheterocycles

Y Song, G Wei, Z Quan, Z Chen, XF Wu - Organic Chemistry Frontiers, 2023 - pubs.rsc.org
An expedient and efficient approach for the synthesis of structurally diverse carbonyl-
bridged bisheterocycles has been developed via a palladium-catalyzed four-component …

Heterocycle compounds with antimicrobial activity

M Fesatidou, A Petrou, G Athina - Current pharmaceutical …, 2020 - ingentaconnect.com
Background: Bacterial infections are a growing problem worldwide causing morbidity and
mortality mainly in developing countries. Moreover, the increased number of …

Synthesis and antiproliferative activity of some new fluorinated Schiff bases derived from 1, 2, 4-triazoles

BNP Kumar, KN Mohana, L Mallesha - Journal of Fluorine Chemistry, 2013 - Elsevier
Abstract In the present study, 2, 6-diflurobenzohydrazide 1 and 4-fluorophenylisothiocyanate
were used as the starting materials to synthesize 5-(2, 6-diflurophenyl)-N 3-(4-fluorophenyl) …