Synthetically-tailored and nature-derived dual COX-2/5-LOX inhibitors: Structural aspects and SAR

MA Meshram, UO Bhise, PN Makhal, VR Kaki - European Journal of …, 2021 - Elsevier
Inflammation is a most complex pathological process that gives birth to different diseases.
Different inflammatory mediators are released during an inflammation responsible for acute …

Design and Development of COX-II Inhibitors: Current Scenario and Future Perspective

S Chahal, P Rani, Kiran, J Sindhu, G Joshi… - ACS …, 2023 - ACS Publications
Innate inflammation beyond a threshold is a significant problem involved in cardiovascular
diseases, cancer, and many other chronic conditions. Cyclooxygenase (COX) enzymes are …

Novel class of benzimidazole-thiazole hybrids: The privileged scaffolds of potent anti-inflammatory activity with dual inhibition of cyclooxygenase and 15-lipoxygenase …

MTE Maghraby, OMF Abou-Ghadir… - Bioorganic & medicinal …, 2020 - Elsevier
The present study includes design and synthesis of new molecular hybrids of 2-
methylthiobenzimidazole linked to various anti-inflammatory pharmacophores through 2 …

Synthesis, biological evaluation and docking study of 1, 3, 4-thiadiazole-thiazolidinone hybrids as anti-inflammatory agents with dual inhibition of COX-2 and 15-LOX

YM Omar, HHM Abdu-Allah, SG Abdel-Moty - Bioorganic chemistry, 2018 - Elsevier
Selective inhibition of both cyclooxygenase-2 (COX-2) and 15-lipooxygenase (15-LOX) may
provide good strategy for alleviation of inflammatory disorders while minimizing side effects …

Evaluation of the in vitro anti-inflammatory and cytotoxic potential of ethanolic and aqueous extracts of Origanum syriacum and Salvia lanigera leaves

MA Alonazi, I Jemel, N Moubayed, M Alwhibi… - … Science and Pollution …, 2021 - Springer
In this study, the chemical compositions of the ethanolic and aqueous extracts of the leaves
of Origanum syriacum and Salvia lanigera were identified based on GC-MS spectrometric …

Synthesis and biological evaluation of pyrazolone analogues as potential anti‐inflammatory agents targeting cyclooxygenases and 5‐lipoxygenase

MA Shabaan, AM Kamal, SI Faggal… - Archiv der …, 2020 - Wiley Online Library
New pyrazolone derivatives structurally related to celecoxib and FPL 62064 were
synthesized and biologically evaluated for their inhibitory activity against cyclooxygenases …

Rational design of biodegradable sulphonamide candidates treating septicaemia by synergistic dual inhibition of COX-2/PGE2 axis and DHPS enzyme

NH El-Dershaby, SA El-Hawash… - Journal of Enzyme …, 2022 - Taylor & Francis
A new series of co-drugs was designed based on hybridising the dihydropteroate synthase
(DHPS) inhibitor sulphonamide scaffold with the COX-2 inhibitor salicylamide …

Synthesis, biological evaluation and docking studies of N-substituted resveratrol derivatives

H Wu, L Liu, M Song, X Yin, M Chen, G Lv, F Zhao… - Fitoterapia, 2024 - Elsevier
A total of 19 resveratrol derivatives, including 12 imines and 7 amines, were synthesized,
among which compounds 1, 5, 6, 7′, 11′, and 13 are new compounds. The anti …

Combining lavendustin C and 5-arylidenethiazolin-4-one-based pharmacophores toward multitarget anticancer hybrids

SA Othman, OF Abou-Ghadir, V Menon… - Bioorganic …, 2024 - Elsevier
Lavendustin C, a natural-product derived anticancer lead compound, was modified at its
carboxylic group by esterification or amidation (compounds 6–10) and at its amino group by …

Conjugation of 4-aminosalicylate with thiazolinones afforded non-cytotoxic potent in vitro and in vivo anti-inflammatory hybrids

HHM Abdu-Allah, AAB Abdelmoez, H Tarazi… - Bioorganic …, 2020 - Elsevier
Eicosanoids like leukotrienes and prostaglandins that produced within the arachidonic acid
cascade are involved in the pathogenesis of pain, acute and chronic inflammatory diseases …