Design and Synthesis of l-1′-Homologated Adenosine Derivatives as Potential Anti-inflammatory Agents

M Nguyen, MA Aslam, Y Nguyen, HMA Javaid… - ACS …, 2023 - ACS Publications
Inflammatory responses are fundamental protective warning mechanisms. However, in
certain instances, they contribute significantly to the development of several chronic …

Design, Synthesis, and Biological Activity of l-1′-Homologated Adenosine Derivatives

M Nguyen, S An, Y Nguyen, YE Hyun… - ACS Medicinal …, 2022 - ACS Publications
On the basis of the previously reported polypharmacological profile of truncated d-1′-
homologated adenosine derivatives [J. Med. Chem. 2020, 63, 16012], the l-nucleoside …

Three Arachidonoylamide Derivatives Inhibit Pro-Inflammatory Genes Expression by Modulating NF-ΚB and AP1 Activities

A Gregorelli, A Sgarbossa, S Khan… - Medicinal …, 2016 - ingentaconnect.com
Background: Since the anti-inflammatory activity of arachidonic acid derivatives was
previously reported, we synthesized three new amide derivatives of arachidonic acid (AA …

Advances in the mechanisms and applications of inhibitory oligodeoxynucleotides against immune-mediated inflammatory diseases

H Wang, Y Su, D Chen, Q Li, S Shi, X Huang… - Frontiers in …, 2023 - frontiersin.org
Inhibitory oligodeoxynucleotides (ODNs) are short single-stranded DNA, which capable of
folding into complex structures, enabling them to bind to a large variety of targets. With …

Structural modifications yield novel insights into the intriguing pharmacodynamic potential of anti-inflammatory nitro-fatty acids

N Hellmuth, C Brat, O Awad, S George… - Frontiers in …, 2021 - frontiersin.org
Endogenous nitro-fatty acids (NFA) are potent electrophilic lipid mediators that exert
biological effects in vitro and in vivo via selective covalent modification of thiol-containing …

3-Deazaadenosine, an S-adenosylhomocysteine hydrolase inhibitor, attenuates lipopolysaccharide-induced inflammatory responses via inhibition of AP-1 and NF-κB …

WS Yang, JH Kim, D Jeong, YH Hong, SH Park… - Biochemical …, 2020 - Elsevier
Deazadenosine (3-DA) is a general methylation inhibitor that depletes S-
adenosylmethionine, a methyl donor, by blocking S-adenosylhomocysteine hydrolase …

Adenosine and a related carbocyclic nucleoside analogue selectively inhibit tumor necrosis factor-alpha production and protect mice against endotoxin challenge.

MJ Parmely, WW Zhou, CK Edwards 3rd… - … (Baltimore, Md.: 1950 …, 1993 - journals.aai.org
Adenosine (ADO) and its structurally related analogues are known to regulate the activities
of immune and inflammatory cells, including a number of key functions of mononuclear …

Synthesis and discovery of ω-3 polyunsaturated fatty acid-alkanolamine (PUFA-AA) derivatives as anti-inflammatory agents targeting Nur77

H Fang, J Zhang, M Ao, F He, W Chen, Y Qian… - Bioorganic …, 2020 - Elsevier
In this work, three series of ω-3 polyunsaturated fatty acid-alkanolamine derivatives (PUFA-
AAs) were synthesized, characterized and their anti-inflammatory activity in vivo was …

Discovery of new DHA ethanolamine derivatives as potential anti-inflammatory agents targeting Nur77

H Fang, M Li, X Wang, W Chen, F He, Y Zhang… - Bioorganic …, 2023 - Elsevier
Docosahexaenoic acid (DHA) has a strong anti-inflammatory effect and is reported to bind to
the ligand-binding domain (LBD) of the anti-inflammatory modulator Nur77. Recently, we …

Discovery of 2-substituted 3-arylquinoline derivatives as potential anti-inflammatory agents through inhibition of LPS-induced inflammatory responses in macrophages

CY Yang, YL Hung, KW Tang, SC Wang, CH Tseng… - Molecules, 2019 - mdpi.com
We describe herein the preparation of certain 2-substituted 3-arylquinoline derivatives and
the evaluation of their anti-inflammatory effects in LPS-activated murine J774A. 1 …