Antonello Mai

Sapienza University of Rome

Italy

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Articles (20)

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2025

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Collaborators (15)

Donatella Del Bufalo

Istituto Regina Elena

ITALY

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Clemens Zwergel

Assistant Professor RTD-A

Sapienza University of Rome

ITALY

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Angela NEBBIOSO

Associate Professor

Università degli Studi della Campania Luigi Vanvitelli

ITALY

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Matteo Russo

ITALY

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Claus Jacob

Saarland University

GERMANY

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Marco Tafani

Associate Professor

Università degli Studi di Roma La Sapienza Facoltà di Medicina e Odontoiatria

ITALY

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rossella fioravanti

University

ITALY

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Elisabetta Ferretti

Full Professor

Sapienza University of Rome

ITALY

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Claudiu T Supuran

University of Florence

ITALY

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Christian Ducho

Full Professor

Saarland University

GERMANY

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Dante Rotili

Sapienza University of Rome

ITALY

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Alice Conigliaro

Professore Associato

Università degli Studi di Palermo

ITALY

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Marco Tripodi

Sapienza University of Rome

ITALY

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Maria Eduarda Mendes

Assistant Professor

Faculty of Pharmacy

PORTUGAL

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Lucia Altucci

University of Campania “Luigi Vanvitelli”

ITALY

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Antonello Mai

Research Interests

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Articles (20)

Long noncoding RNA H19 promotes the acquisition of a mesenchymal-like invasive phenotype in mesothelial primary cells through an HDAC1-mediated WT1/Sp1 switch

Advancements in Hydrazide-Based HDAC Inhibitors: A Review of Recent Developments and Therapeutic Potential

Development of C646‐Based Proteolysis Targeting Chimeras Degraders of the Lysine Acetyltransferases CBP and p300

Native mass spectrometry for proximity-inducing compounds: a new opportunity for studying chemical-induced protein modulation

An Amazing 30-Year Journey around the DABO Family: A Medicinal Chemistry Lesson on a Versatile Class of Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors

SIRT3 Activation a Promise in Drug Development? New Insights into SIRT3 Biology and Its Implications on the Drug Discovery Process

Heterocycles–Containing HDAC Inhibitors Active in Cancer: An Overview of the Last Fifteen Years

Correction: Zwergel et al. Novel Quinoline Compounds Active in Cancer Cells through Coupled DNA Methyltransferase Inhibition and Degradation. Cancers 2020, 12, 447

Activation and inhibition of sirtuins: From bench to bedside

Pharmacological Activation of SIRT3 Modulates the Response of Cancer Cells to Acidic pH

GreenMedChem: the challenge in the next decade toward eco-friendly compounds and processes in drug design

Role of SIRT3 in Microgravity Response: A New Player in Muscle Tissue Recovery

SIRT5 Activation and Inorganic Phosphate Binding Reduce Cancer Cell Vitality by Modulating Autophagy/Mitophagy and ROS

Antihistamines, phenothiazine-based antipsychotics, and tricyclic antidepressants potently activate pharmacologically relevant human carbonic anhydrase isoforms II and VII

Simultaneous administration of EZH2 and BET inhibitors inhibits proliferation and clonogenic ability of metastatic prostate cancer cells

Histone deacetylase 10: A polyamine deacetylase from the crystal structure to the first inhibitors

The role of structural biology in the design of sirtuin activators

Comparative Study of Adenosine Analogs as Inhibitors of Protein Arginine Methyltransferases and a Clostridioides difficile-Specific DNA Adenine Methyltransferase

Emerging Roles of SIRT5 in Metabolism, Cancer, and SARS-CoV-2 Infection

METTL3 from Target Validation to the First Small-Molecule Inhibitors: A Medicinal Chemistry Journey

Collaborators (15)

Donatella Del Bufalo

Clemens Zwergel

Angela NEBBIOSO

Matteo Russo

Claus Jacob

Marco Tafani

rossella fioravanti

Elisabetta Ferretti

Claudiu T Supuran

Christian Ducho

Dante Rotili

Alice Conigliaro

Marco Tripodi

Maria Eduarda Mendes

Lucia Altucci

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