| Literature DB >> 33334192 |
Elisabetta Barresi1, Chiara Giacomelli1, Laura Marchetti1, Emma Baglini1, Silvia Salerno1, Giovanni Greco2, Federico Da Settimo1, Claudia Martini1, Maria Letizia Trincavelli1, Sabrina Taliani1.
Abstract
Small-molecules acting as positive allosteric modulators (PAMs) of the A2B adenosine receptor (A2B AR) could potentially represent a novel therapeutic strategy for pathological conditions characterised by altered bone homeostasis, including osteoporosis. We investigated a library of compounds (4-13) exhibiting different degrees of chemical similarity with three indole derivatives (1-3), which have been recently identified by us as PAMs of the A2B AR able to promote mesenchymal stem cell differentiation and bone formation. Evaluation of mineralisation activity of 4-13 in the presence and in the absence of the agonist BAY60-6583 allowed the identification of lead compounds with therapeutic potential as anti-osteoporosis agents. Further biological characterisation of one of the most performing compounds, the benzofurane derivative 9, confirmed that such a molecule behaves as PAM of the A2B AR.Entities:
Keywords: A2B adenosine receptor; BAY60-6583; allosteric modulators; bone formation; mesenchymal stem cell
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Year: 2021 PMID: 33334192 PMCID: PMC7751416 DOI: 10.1080/14756366.2020.1862103
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051