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antonello.mai@uniroma1.it
Antonello Mai
Professore Ordinario
Struttura:
DIPARTIMENTO DI CHIMICA E TECNOLOGIE DEL FARMACO
E-mail:
antonello.mai@uniroma1.it
Pagina istituzionale corsi di laurea
Curriculum Sapienza
Publications
Title
Published on
Year
A Xanthine Derivative With Novel Heat Shock Protein 90-Alpha Inhibitory and Senolytic Properties
AGING CELL
2025
HDAC1/2 control mesothelium/ovarian cancer adhesive interactions impacting on Talin-1-α5β1-integrin-mediated actin cytoskeleton and extracellular matrix protein remodeling
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
2024
SIRT3 Activation a Promise in Drug Development? New Insights into SIRT3 Biology and Its Implications on the Drug Discovery Process
JOURNAL OF MEDICINAL CHEMISTRY
2024
Mechanisms of mesothelial cell response to viral infections: HDAC1-3 inhibition blocks poly(I:C)-induced type I interferon response and modulates the mesenchymal/inflammatory phenotype
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
2024
Specific Inhibitors of Mitochondrial Deacylase Sirtuin 4 Endowed with Cellular Activity
JOURNAL OF MEDICINAL CHEMISTRY
2024
Targeting of H19/cell adhesion molecules circuitry by GSK-J4 epidrug inhibits metastatic progression in prostate cancer
CANCER CELL INTERNATIONAL
2024
Theileria parasites sequester host eIF5A to escape elimination by host-mediated autophagy
NATURE COMMUNICATIONS
2024
Uracil- and Pyridine-Containing HDAC Inhibitors Displayed Cytotoxicity in Colorectal and Glioblastoma Cancer Stem Cells
CHEMMEDCHEM
2024
Heterocycles-Containing HDAC Inhibitors Active in Cancer: An Overview of the Last Fifteen Years
CHEMMEDCHEM
2024
A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in human macrophages and in a mouse model of infection
PLOS BIOLOGY
2024
m6A modification inhibits miRNAs’ intracellular function, favoring their extracellular export for intercellular communication
CELL REPORTS
2024
STRUCTURE-BASED MECHANISM OF RIBOREGULATION OF THE METABOLIC ENZYME SHMT1
MOLECULAR CELL
2024
Pharmacological Activation of SIRT3 Modulates the Response of Cancer Cells to Acidic pH
PHARMACEUTICALS
2024
HDAC3 genetic and pharmacologic inhibition radiosensitizes fusion positive rhabdomyosarcoma by promoting DNA double-strand breaks
CELL DEATH DISCOVERY
2024
Off-target inhibition of human dihydroorotate dehydrogenase (hDHODH) highlights challenges in the development of fat mass and obesity-associated protein (FTO) inhibitors
ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE
2024
Activation and inhibition of sirtuins: From bench to bedside
MEDICINAL RESEARCH REVIEWS
2024
Successes and challenges in the development of BD1-selective BET inhibitors: a patent review
EXPERT OPINION ON THERAPEUTIC PATENTS
2024
Systematic Design of Adenosine Analogs as Inhibitors of a Clostridioides difficile-Specific DNA Adenine Methyltransferase Required for Normal Sporulation and Persistence
JOURNAL OF MEDICINAL CHEMISTRY
2023
METTL3 from Target Validation to the First Small-Molecule Inhibitors: A Medicinal Chemistry Journey
JOURNAL OF MEDICINAL CHEMISTRY
2023
Simultaneous administration of EZH2 and BET inhibitors inhibits proliferation and clonogenic ability of metastatic prostate cancer cells
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
2023
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ERC
PE5_18
KET
Life-science technologies & biotechnologies
Interessi di ricerca
Keywords
drug discovery
Epigenetic drugs
antiviral agents
Anticancer drugs
parasite growth inhibition
Progetti di Ricerca
Italian Centre for Native Mass Spectrometry - INCENTIVE MS
Dual- and multi-targeting epigenetic inhibitors for the treatment of aggressive and/or recurrent cancers.
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