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An integrated drug repurposing strategy for the rapid identification of potential SARS-CoV-2 viral inhibitors

Scientific reports, 2020-08, Vol.10 (1), p.13866-13866, Article 13866

2020

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A Drug Discovery Approach to a Reveal Novel Antioxidant Natural Source: The Case of Chestnut Burr Biomass

International journal of molecular sciences, 2024-03, Vol.25 (5), p.2517

2024

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Pharmacological and In Silico Analysis of Oat Avenanthramides as EGFR Inhibitors: Effects on EGF-Induced Lung Cancer Cell Growth and Migration

International journal of molecular sciences, 2022-08, Vol.23 (15), p.8534

2022

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Dissecting the CD93-Multimerin 2 interaction involved in cell adhesion and migration of the activated endothelium

Matrix biology, 2017-12, Vol.64, p.112-127

2017

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Ritanserin blocks CaV1.2 channels in rat artery smooth muscles: electrophysiological, functional, and computational studies

Acta pharmacologica Sinica, 2020-09, Vol.41 (9), p.1158-1166

2020

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Vietnamese Dalbergia tonkinensis: A Promising Source of Mono- and Bifunctional Vasodilators

Molecules (Basel, Switzerland), 2022-07, Vol.27 (14), p.4505

2022

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In Silico Multi-Target Approach Revealed Potential Lead Compounds as Scaffold for the Synthesis of Chemical Analogues Targeting SARS-CoV-2

Biology (Basel, Switzerland), 2022-03, Vol.11 (3), p.465

2022

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A Computational Approach From Gene to Structure Analysis of the Human ABCA4 Transporter Involved in Genetic Retinal Diseases

Investigative ophthalmology & visual science, 2017-10, Vol.58 (12), p.5320-5328

2017

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Machine learning application for development of a data-driven predictive model able to investigate quality of life scores in a rare disease

Orphanet journal of rare diseases, 2020-02, Vol.15 (1), p.46-46, Article 46

2020

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Novel Labdane Diterpenes-Based Synthetic Derivatives: Identification of a Bifunctional Vasodilator That Inhibits CaV1.2 and Stimulates KCa1.1 Channels

Marine drugs, 2022-08, Vol.20 (8), p.515

2022

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2-Hydroxy-5-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate: Synthesis, In Silico Analysis and In Vitro Pharmacological Evaluation

MolBank, 2021-09, Vol.2021 (3), p.M1258

2021

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From in silico to in vitro: a trip to reveal flavonoid binding on the Rattus norvegicus Kir6.1 ATP-sensitive inward rectifier potassium channel

PeerJ (San Francisco, CA), 2018-05, Vol.6, p.e4680-e4680, Article e4680

2018

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The Selective Rat Toxicant Norbormide Blocks KATP Channels in Smooth Muscle Cells But Not in Insulin-Secreting Cells

Frontiers in pharmacology, 2019-05, Vol.10, p.598-598

2019

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A possible strategy to fight COVID-19: Interfering with spike glycoprotein trimerization

Biochemical and biophysical research communications, 2020-07, Vol.528 (1), p.35-38

2020

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The surge of flavonoids as novel, fine regulators of cardiovascular Ca v channels

European journal of pharmacology, 2017-02, Vol.796, p.158

2017

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The drp-1-mediated mitochondrial fission inhibitor mdivi-1 impacts the function of ion channels and pathways underpinning vascular smooth muscle tone

Biochemical pharmacology, 2022-09, Vol.203, p.115205-115205, Article 115205

2022

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Cav1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies

Biochemical pharmacology, 2017-09, Vol.140, p.53-63

2017

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Flavonoids and hERG channels: Friends or foes?

European journal of pharmacology, 2021-05, Vol.899, p.174030, Article 174030

2021

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Identification of Inhibitors Binding Site of Ebola L Polymerase Based on its Homology Model

Journal of Virology & Antiviral Research, 2016, Vol.5 (4)

Trezza, Alfonso

2016

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Dynamin-independent CaV1.2 and KCa1.1 channels regulation and vascular tone modulation by the mitochondrial fission inhibitors dynasore and dyngo-4a

European journal of pharmacology, 2023-07, Vol.951, p.175786-175786, Article 175786

2023

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A multitarget semi-synthetic derivative of the flavonoid morin with improved in vitro vasorelaxant activity: Role of CaV1.2 and KCa1.1 channels

Biochemical pharmacology, 2021-03, Vol.185, p.114429-114429, Article 114429

2021

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ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

European journal of human genetics : EJHG, 2020-11, Vol.28 (11), p.1602-1614

2020

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Ca v 1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies

Biochemical pharmacology, 2017-09, Vol.140, p.53-63

2017

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Structural Bioinformatic Survey of Protein-Small Molecule Interfaces Delineates the Role of Glycine in Surface Pocket Formation

IEEE/ACM transactions on computational biology and bioinformatics, 2022-05, Vol.19 (3), p.1881-1886

2022

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Artificial intelligence-driven identification of morin analogues acting as CaV1.2 channel blockers: Synthesis and biological evaluation

Bioorganic chemistry, 2023-02, Vol.131, p.106326-106326, Article 106326

2023

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An integrated drug repurposing strategy for the rapid identification of potential SARS-CoV-2 viral inhibitors

A Drug Discovery Approach to a Reveal Novel Antioxidant Natural Source: The Case of Chestnut Burr Biomass

Pharmacological and In Silico Analysis of Oat Avenanthramides as EGFR Inhibitors: Effects on EGF-Induced Lung Cancer Cell Growth and Migration

Dissecting the CD93-Multimerin 2 interaction involved in cell adhesion and migration of the activated endothelium

Ritanserin blocks CaV1.2 channels in rat artery smooth muscles: electrophysiological, functional, and computational studies

Vietnamese Dalbergia tonkinensis: A Promising Source of Mono- and Bifunctional Vasodilators

In Silico Multi-Target Approach Revealed Potential Lead Compounds as Scaffold for the Synthesis of Chemical Analogues Targeting SARS-CoV-2

A Computational Approach From Gene to Structure Analysis of the Human ABCA4 Transporter Involved in Genetic Retinal Diseases

Machine learning application for development of a data-driven predictive model able to investigate quality of life scores in a rare disease

Novel Labdane Diterpenes-Based Synthetic Derivatives: Identification of a Bifunctional Vasodilator That Inhibits CaV1.2 and Stimulates KCa1.1 Channels

2-Hydroxy-5-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl (E)-3-(4-hydroxy-3-methoxyphenyl)acrylate: Synthesis, In Silico Analysis and In Vitro Pharmacological Evaluation

From in silico to in vitro: a trip to reveal flavonoid binding on the Rattus norvegicus Kir6.1 ATP-sensitive inward rectifier potassium channel

The Selective Rat Toxicant Norbormide Blocks KATP Channels in Smooth Muscle Cells But Not in Insulin-Secreting Cells

A possible strategy to fight COVID-19: Interfering with spike glycoprotein trimerization

The surge of flavonoids as novel, fine regulators of cardiovascular Ca v channels

The drp-1-mediated mitochondrial fission inhibitor mdivi-1 impacts the function of ion channels and pathways underpinning vascular smooth muscle tone

Cav1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies

Flavonoids and hERG channels: Friends or foes?

Identification of Inhibitors Binding Site of Ebola L Polymerase Based on its Homology Model

Dynamin-independent CaV1.2 and KCa1.1 channels regulation and vascular tone modulation by the mitochondrial fission inhibitors dynasore and dyngo-4a

A multitarget semi-synthetic derivative of the flavonoid morin with improved in vitro vasorelaxant activity: Role of CaV1.2 and KCa1.1 channels

ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

Ca v 1.2 channel current block by the PKA inhibitor H-89 in rat tail artery myocytes via a PKA-independent mechanism: Electrophysiological, functional, and molecular docking studies

Structural Bioinformatic Survey of Protein-Small Molecule Interfaces Delineates the Role of Glycine in Surface Pocket Formation

Artificial intelligence-driven identification of morin analogues acting as CaV1.2 channel blockers: Synthesis and biological evaluation

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