Ross P. Mcgeary

Brisbane, QLD 4072, Australia

Last Updated: 09/26/2026

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Found 44 publications

A Ketol-Acid Reductoisomerase Inhibitor That Has Antituberculosis and Herbicidal Activity.

A Ketol-Acid Reductoisomerase Inhibitor That Has Antituberculosis and Herbicidal Activity.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: March 24, 2025

Inhibitors for metallo-β-lactamases from the B1 and B3 subgroups provide an avenue to combat a major mechanism of antibiotic resistance.

Inhibitors for metallo-β-lactamases from the B1 and B3 subgroups provide an avenue to combat a major mechanism of antibiotic resistance.

Journal: Bioorganic & medicinal chemistry letters

Published: April 17, 2023

Optimization of an α-aminonaphthylmethylphosphonic acid inhibitor of purple acid phosphatase using rational structure-based design approaches.

Optimization of an α-aminonaphthylmethylphosphonic acid inhibitor of purple acid phosphatase using rational structure-based design approaches.

Journal: European journal of medicinal chemistry

Published: November 23, 2022

Rational Design of Potent Inhibitors of a Metallohydrolase Using a Fragment-Based Approach.

Rational Design of Potent Inhibitors of a Metallohydrolase Using a Fragment-Based Approach.

Journal: ChemMedChem

Published: July 12, 2021

Analogues of the Herbicide, N-Hydroxy-N-isopropyloxamate, Inhibit Mycobacterium tuberculosis Ketol-Acid Reductoisomerase and Their Prodrugs Are Promising Anti-TB Drug Leads.

Analogues of the Herbicide, N-Hydroxy-N-isopropyloxamate, Inhibit Mycobacterium tuberculosis Ketol-Acid Reductoisomerase and Their Prodrugs Are Promising Anti-TB Drug Leads.

Journal: Journal of medicinal chemistry

Published: January 29, 2021

Discovery of a Pyrimidinedione Derivative with Potent Inhibitory Activity against Mycobacterium tuberculosis Ketol-Acid Reductoisomerase.

Discovery of a Pyrimidinedione Derivative with Potent Inhibitory Activity against Mycobacterium tuberculosis Ketol-Acid Reductoisomerase.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: October 21, 2020

Discovery of drug-like acetylcholinesterase inhibitors by rapid virtual screening of a 6.9 million compound database.

Discovery of drug-like acetylcholinesterase inhibitors by rapid virtual screening of a 6.9 million compound database.

Journal: Chemical biology & drug design

Published: October 09, 2020

Rapid discovery of a selective butyrylcholinesterase inhibitor using structure-based virtual screening.

Rapid discovery of a selective butyrylcholinesterase inhibitor using structure-based virtual screening.

Journal: Bioorganic & medicinal chemistry letters

Published: August 09, 2020

Design, synthesis, biological evaluation and in silico studies of certain aryl sulfonyl hydrazones conjugated with 1,3-diaryl pyrazoles as potent metallo-β-lactamase inhibitors.

Design, synthesis, biological evaluation and in silico studies of certain aryl sulfonyl hydrazones conjugated with 1,3-diaryl pyrazoles as potent metallo-β-lactamase inhibitors.

Journal: Bioorganic chemistry

Published: August 05, 2020

Broad spectrum antibiotic-degrading metallo-β-lactamases are phylogenetically diverse.

Broad spectrum antibiotic-degrading metallo-β-lactamases are phylogenetically diverse.

Journal: Protein & cell

Published: June 17, 2020

Inhibition studies of ketol-acid reductoisomerases from pathogenic microorganisms.

Inhibition studies of ketol-acid reductoisomerases from pathogenic microorganisms.

Journal: Archives of biochemistry and biophysics

Published: May 03, 2020

Discovery, Synthesis and Evaluation of a Ketol-Acid Reductoisomerase Inhibitor.

Discovery, Synthesis and Evaluation of a Ketol-Acid Reductoisomerase Inhibitor.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: February 19, 2020

Showing 1-12 of 44

Last Updated: 09/26/2026