| Literature DB >> 33007395 |
Aparna Sundaram1, Chun Chen2, Nilgun Isik Reed1, Sean Liu3, Seul Ki Yeon4, Joel McIntosh4, You-Zhi Tang4, Hyunjun Yang4, Marc Adler5, Richard Beresis5, Ian B Seiple4, Dean Sheppard1, William F DeGrado4, Hyunil Jo6.
Abstract
Inhibition of integrin α5β1 emerges as a novel therapeutic option to block transmission of contractile forces during asthma attack. We designed and synthesized novel inhibitors of integrin α5β1 by backbone replacement of known αvβ1 integrin inhibitors. These integrin α5β1 inhibitors also retain the nanomolar potency against αvβ1 integrin, which shows promise for developing dual integrin α5β1/αvβ1 inhibitor. Introduction of hydrophobic adamantane group significantly boosted the potency as well as selectivity over integrin αvβ3. We also demonstrated one of the inhibitors (11) reduced airway hyperresponsiveness in ex vivo mouse tracheal ring assay. Results from this study will help guide further development of integrin α5β1 inhibitors as potential novel asthma therapeutics.Entities:
Keywords: Asthma; Integrin inhibitor; Integrin α5β1; Integrin αvβ1; RGD integrin
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Year: 2020 PMID: 33007395 PMCID: PMC7700746 DOI: 10.1016/j.bmcl.2020.127578
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823