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Antioxidants (Basel, Switzerland)|November 27, 2021
A Novel Class of Dual-Acting DCH-CORMs Counteracts Oxidative Stress-Induced Inflammation in Human Primary TenocytesFederico Appetecchia, Sara Consalvi, Emanuela Berrino, et al.
Pharmaceutics|March 29, 2023
Antiviral Mechanisms of N-Phenyl Benzamides on Coxsackie Virus A9Mira Laajala, Kerttu Kalander, Sara Consalvi, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|December 13, 2016
Pharmaceutical salt of BM635 with improved bioavailabilityGiovanna Poce, Sara Consalvi, Martina Cocozza, et al.
Pharmaceutics|March 26, 2022
Nano-Based Drug Delivery Systems of Potent MmpL3 Inhibitors for Tuberculosis TreatmentPatrizia Nadia Hanieh, Sara Consalvi, Jacopo Forte, et al.
Seminars in Cancer Biology|August 28, 2019
Dietary flavonoids: Nano delivery and nanoparticles for cancer therapyPaola Aiello, Sara Consalvi, Giovanna Poce, et al.
European Journal of Medicinal Chemistry|September 14, 2021
6-Fluorophenylbenzohydrazides inhibit Mycobacterium tuberculosis growth through alteration of tryptophan biosynthesisSara Consalvi, Giulia Venditti, Junhao Zhu, et al.
Chemmedchem|May 28, 2016
A Series of COX-2 Inhibitors Endowed with NO-Releasing Properties: Synthesis, Biological Evaluation, and Docking AnalysisSara Consalvi, Giovanna Poce, Rino Ragno, et al.
European Journal of Medicinal Chemistry|November 10, 2020
Therapeutic potential for coxibs-nitric oxide releasing hybrids in cystic fibrosisSara Consalvi, Giovanna Poce, Carla Ghelardini, et al.
European Journal of Medicinal Chemistry|January 17, 2018
In vivo potent BM635 analogue with improved drug-like propertiesGiovanna Poce, Martina Cocozza, Salvatore Alfonso, et al.
Bioorganic & Medicinal Chemistry|January 19, 2015
Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitorsSara Consalvi, Salvatore Alfonso, Angela Di Capua, et al.
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