Ines Bruno
Affiliations: | University of Salerno |
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| Pierri M, Bove G, Gazzillo E, et al. (2025) Unveiling New Triazoloquinoxaline-based PROTACs Designed for the Selective Degradation of the ncBAF Chromatin Remodeling Subunit BRD9. Chemistry (Weinheim An Der Bergstrasse, Germany). e202404218 |
| Nardone V, Ruggiero D, Chini MG, et al. (2025) From Bench to Bedside: Translational Approaches to Cardiotoxicity in Breast Cancer, Lung Cancer, and Lymphoma Therapies. Cancers. 17 |
| Ruggiero D, Ingenito E, Boccia E, et al. (2025) Identification of the first-in-class dual inhibitor targeting BAG3 and HSP70 proteins to disrupt multiple chaperone pathways. European Journal of Medicinal Chemistry. 287: 117358 |
| Ruggiero D, Ingenito E, Boccia E, et al. (2024) Identification of a New Promising BAG3 Modulator Featuring the Imidazopyridine Scaffold. Molecules (Basel, Switzerland). 29 |
| Di Micco S, Ruggiero D, Terracciano S, et al. (2024) Identification of honokiol-based scaffold to design tankyrase 1/2 inhibitors by in silico and in vitro studies. Chemistry & Biodiversity. e202401854 |
| Colarusso E, Gazzillo E, Boccia E, et al. (2024) Identification of Novel Bromodomain-Containing Protein 4 (BRD4) Binders through 3D Pharmacophore-Based Repositioning Screening Campaign. Molecules (Basel, Switzerland). 29 |
| Colarusso E, Gazzillo E, Pierri M, et al. (2024) In Silico Design, Chemical Synthesis, Biophysical and In Vitro Evaluation for the Identification of 1-ethyl-1H-pyrazolo[3,4-b]pyridine-based BRD9 Binders. Chempluschem. e202400339 |
| Gazzillo E, Pierri M, Colarusso E, et al. (2023) Exploring the chemical space of functionalized [1,2,4]triazolo[4,3-a]quinoxaline-based compounds targeting the bromodomain of BRD9. Bioorganic Chemistry. 139: 106677 |
| Morretta E, Ruggiero D, Belvedere R, et al. (2023) A multidisciplinary functional proteomics-aided strategy as a tool for the profiling of a novel cytotoxic thiadiazolopyrimidone. Bioorganic Chemistry. 138: 106620 |
| Potenza M, Giordano A, Chini MG, et al. (2022) Identification of 2-Aminoacyl-1,3,4-thiadiazoles as Prostaglandin E and Leukotriene Biosynthesis Inhibitors. Acs Medicinal Chemistry Letters. 14: 26-34 |