Davide Capelli
Rome, 34149, Italy
Last Updated: 09/26/2026
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Found 25 publications
Correction to "Novel N-(Heterocyclylphenyl)benzensulfonamide Sharing an Unreported Binding Site with T-Cell Factor 4 at the β-Catenin Armadillo Repeats Domain as Anticancer Agent".
Journal: ACS pharmacology & translational science
Published: March 08, 2025
Enhancing the activity of γ-hydroxy lactone derivatives as innovative peroxisome proliferator-activated receptor γ non-agonists inhibiting cyclin-dependent kinase 5-mediated phosphorylation.
Journal: European journal of medicinal chemistry
Published: February 25, 2025
Corrigendum to "A chemical modification of a peroxisome proliferator-activated receptor pan agonist produced a shift to a new dual alpha/gamma partial agonist endowed with mitochondrial pyruvate carrier inhibition and antidiabetic properties" [Eur. J. Med. Chem. 275 (2024) 116567].
Journal: European journal of medicinal chemistry
Published: February 13, 2025
A chemical modification of a peroxisome proliferator-activated receptor pan agonist produced a shift to a new dual alpha/gamma partial agonist endowed with mitochondrial pyruvate carrier inhibition and antidiabetic properties.
Journal: European journal of medicinal chemistry
Published: April 12, 2024
Development of an analytical platform for the affinity screening of natural extracts by SEC-MS towards PPARα and PPARγ receptors.
Journal: Analytica chimica acta
Published: February 15, 2024
Novel N-(Heterocyclylphenyl)benzensulfonamide Sharing an Unreported Binding Site with T-Cell Factor 4 at the β-Catenin Armadillo Repeats Domain as an Anticancer Agent.
Journal: ACS pharmacology & translational science
Published: May 17, 2023
Electrochemical and Structural Characterization of Lanthanum-Doped Hydroxyapatite: A Promising Material for Sensing Applications.
Journal: Materials (Basel, Switzerland)
Published: May 08, 2023
Biological Screening and Crystallographic Studies of Hydroxy γ-Lactone Derivatives to Investigate PPARγ Phosphorylation Inhibition.
Journal: Biomolecules
Published: February 24, 2023
PHA-680626 Is an Effective Inhibitor of the Interaction between Aurora-A and N-Myc.
Journal: International journal of molecular sciences
Published: October 20, 2021
Cytosolic localization and in vitro assembly of human de novo thymidylate synthesis complex.
Journal: The FEBS journal
Published: August 21, 2021
Discovery of Novel Chemical Series of OXA-48 β-Lactamase Inhibitors by High-Throughput Screening.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: May 17, 2021
A Novel N-Substituted Valine Derivative with Unique Peroxisome Proliferator-Activated Receptor γ Binding Properties and Biological Activities.
Journal: Journal of medicinal chemistry
Published: November 03, 2020
Last Updated: 09/26/2026