Artikel ; Online: Synthetic molecules as P2X7 receptor antagonists: A medicinal chemistry update focusing the therapy of inflammatory diseases.
European journal of pharmacology
2023 Band 957, Seite(n) 175999
Abstract: Stimulation of the P2X7 receptor by extracellular adenosine 5'-triphosphate induces a series of responses in the organism, exceptionally protein cascades related to the proinflammatory process. This has made P2X7 a target for research on inflammatory ... ...
Abstract | Stimulation of the P2X7 receptor by extracellular adenosine 5'-triphosphate induces a series of responses in the organism, exceptionally protein cascades related to the proinflammatory process. This has made P2X7 a target for research on inflammatory diseases such as rheumatoid arthritis. Thus, the incessant search for new prototypes that aim to antagonize the action of P2X7 has been remarkable in recent decades, a factor that has already led to numerous clinical studies in humans. In this review, we present the key molecules developed over the years with potential inhibition of P2X7 and inflammation. In addition, an update with newly developed chemical classes with promising activity and results in clinical studies for human pathologies focusing on P2X7 inhibition. |
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Mesh-Begriff(e) | Humans ; Purinergic P2X Receptor Antagonists/pharmacology ; Purinergic P2X Receptor Antagonists/therapeutic use ; Chemistry, Pharmaceutical ; Adenosine Triphosphate ; Arthritis, Rheumatoid ; Inflammation/drug therapy |
Chemische Substanzen | Purinergic P2X Receptor Antagonists ; Adenosine Triphosphate (8L70Q75FXE) |
Sprache | Englisch |
Erscheinungsdatum | 2023-08-22 |
Erscheinungsland | Netherlands |
Dokumenttyp | Journal Article ; Review |
ZDB-ID | 80121-5 |
ISSN | 1879-0712 ; 0014-2999 |
ISSN (online) | 1879-0712 |
ISSN | 0014-2999 |
DOI | 10.1016/j.ejphar.2023.175999 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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