Summer Sale

Up to 30% off — ends 7 Aug

ONLY00h00m00s

Get 30% Off

Up to 30% off — ends 7 Aug

ONLY00h00m00s

Emilia Caselli

Associate Professor

University of Modena and Reggio Emilia

Italy

This profile is automatically generated from trusted academic sources.

Google Scholar

ORCID

How do I reach out?

Meet Kite AI

Contact this professor

ORCID

Google Scholar

Research Interests

Pharmaceutical Chemistry

70%

Pharmacology

10%

Bioactive Compound

40%

Heterocyclic Chemistry

30%

Antibacterial Activity

30%

Antibiotic Therapy

30%

Chemical Biology

30%

Ask ApplyKite AI

Start chatting

How can you help me contact this professor?

What are this professor's research interests?

How should I write an email to this professor?

Articles17

Boronate-Based Inhibitors of Penicillin-Binding Proteins: An Underestimated Avenue for Antibiotic Discovery?

Article Link

Year:

2025

Discovery of Boronic Acids-Based β-Lactamase Inhibitors Through In Situ Click Chemistry

Article Link

Year:

2025

Restoring cefepime activity against multidrug-resistant KPC-producing Klebsiella pneumoniae by combination with boronic acid inhibitors, MB076 and S02030

Article Link

Year:

2025

α‐ Triazolylboronic acids: a novel scaffold to target FLT3 in AML

Article Link

Year:

2024

Defining the minimum inhibitory concentration of 22 rifamycins in iron limited, physiologic medium against Acinetobacter baumannii, Escherichia coli, and Klebsiella pneumoniae clinical isolates

Article Link

Year:

2023

Sulfonamidoboronic Acids as “Cross-Class” Inhibitors of an Expanded-Spectrum Class C Cephalosporinase, ADC-33, and a Class D Carbapenemase, OXA-24/40: Strategic Compound Design to Combat Resistance in Acinetobacter baumannii

Article Link

Year:

2023

Synthesis of a Novel Boronic Acid Transition State Inhibitor, MB076: A Heterocyclic Triazole Effectively Inhibits Acinetobacter-Derived Cephalosporinase Variants with an Expanded-Substrate Spectrum

Article Link

Year:

2023

Natural protein engineering in the Ω-loop: the role of Y221 in ceftazidime and ceftolozane resistance in Pseudomonas -derived cephalosporinase

Article Link

Year:

2023

Boronic Acid Transition State Inhibitors as Potent Inactivators of KPC and CTX-M β-Lactamases: Biochemical and Structural Analyses

Article Link

Year:

2023

Straightforward synthesis of chiral non-racemic α-boryl isocyanides

Article Link

Year:

2021

Insights Into the Inhibition of MOX-1 β-Lactamase by S02030, a Boronic Acid Transition State Inhibitor.

Article Link

Year:

2021

1,2,3-Triazolylmethaneboronate: A Structure Activity Relationship Study of a Class of β-Lactamase Inhibitors against Acinetobacter baumannii Cephalosporinase

Article Link

Year:

2020

The β-Lactamase Inhibitor Boronic Acid Derivative SM23 as a New Anti-Pseudomonas aeruginosa Biofilm

Article Link

Year:

2020

Structural Insights into Inhibition of the Acinetobacter-Derived Cephalosporinase ADC-7 by Ceftazidime and Its Boronic Acid Transition State Analog

Article Link

Year:

2020

A comprehensive and contemporary "snapshot" of β-lactamases in carbapenem resistant Acinetobacter baumannii.

Article Link

Year:

2020

α‐Triazolylboronic Acids: A Promising Scaffold for Effective Inhibitors of KPCs

Article Link

Year:

2020

Structures of FOX-4 Cephamycinase in Complex with Transition-State Analog Inhibitors

Article Link

Year:

2020

Collaborators7

Alfonso Zambon

University of Modena and Reggio Emilia

ITALY

Akiko SHIMIZU-IBUKA

Kanagawa University

JAPAN

Bradley J. Wallar

Grand Valley State University

UNITED STATES

Paolo Zardi

Assistant Professor

University of Padua

ITALY

Brian Luna, PhD

Assistant Professor

University of Southern California Keck School of Medicine

UNITED STATES

Fabio Prati

Full professor

University of Modena and Reggio Emilia

ITALY

Francesco Fini

Associate Professor

University of Modena and Reggio Emilia

ITALY

How do I reach out?

Meet Kite AI

Emilia Caselli

Associate Professor

How do I reach out?

Contact this professor

Research Interests

Ask ApplyKite AI

Articles17

Boronate-Based Inhibitors of Penicillin-Binding Proteins: An Underestimated Avenue for Antibiotic Discovery?

Discovery of Boronic Acids-Based β-Lactamase Inhibitors Through In Situ Click Chemistry

Restoring cefepime activity against multidrug-resistant KPC-producing <i>Klebsiella pneumoniae</i> by combination with boronic acid inhibitors, MB076 and S02030

α‐ Triazolylboronic acids: a novel scaffold to target FLT3 in AML

Defining the minimum inhibitory concentration of 22 rifamycins in iron limited, physiologic medium against Acinetobacter baumannii, Escherichia coli, and Klebsiella pneumoniae clinical isolates

Sulfonamidoboronic Acids as “Cross-Class” Inhibitors of an Expanded-Spectrum Class C Cephalosporinase, ADC-33, and a Class D Carbapenemase, OXA-24/40: Strategic Compound Design to Combat Resistance in <i>Acinetobacter baumannii</i>

Synthesis of a Novel Boronic Acid Transition State Inhibitor, MB076: A Heterocyclic Triazole Effectively Inhibits <i>Acinetobacter</i>-Derived Cephalosporinase Variants with an Expanded-Substrate Spectrum

Natural protein engineering in the Ω-loop: the role of Y221 in ceftazidime and ceftolozane resistance in <i>Pseudomonas</i> -derived cephalosporinase

Boronic Acid Transition State Inhibitors as Potent Inactivators of KPC and CTX-M β-Lactamases: Biochemical and Structural Analyses

Straightforward synthesis of chiral non-racemic α-boryl isocyanides

Insights Into the Inhibition of MOX-1 β-Lactamase by S02030, a Boronic Acid Transition State Inhibitor.

1,2,3-Triazolylmethaneboronate: A Structure Activity Relationship Study of a Class of β-Lactamase Inhibitors against Acinetobacter baumannii Cephalosporinase

The β-Lactamase Inhibitor Boronic Acid Derivative SM23 as a New Anti-Pseudomonas aeruginosa Biofilm

Structural Insights into Inhibition of the Acinetobacter-Derived Cephalosporinase ADC-7 by Ceftazidime and Its Boronic Acid Transition State Analog

A comprehensive and contemporary "snapshot" of β-lactamases in carbapenem resistant Acinetobacter baumannii.

α‐Triazolylboronic Acids: A Promising Scaffold for Effective Inhibitors of KPCs

Structures of FOX-4 Cephamycinase in Complex with Transition-State Analog Inhibitors

Collaborators7

Alfonso Zambon

Akiko SHIMIZU-IBUKA

Bradley J. Wallar

Paolo Zardi

Brian Luna, PhD

Fabio Prati

Francesco Fini

How do I reach out?