As strains of bacteria continuously evolve and become resistant to modern antibiotics, there exists a need for the development of new treatments to combat bacterial infection. Staphylococcus aureus (S. aureus) is known to develop such resistance and remains a leading cause of invasive infections and biofilm formation on prosthetic medical devices. In 2018, Brumley and Spencer et al. isolated anaephenes A–C, natural products from a marine bacterium. Anaephene B was of particular interest as it was the only member of the series to demonstrate moderate antibacterial activity against S. aureus (MIC = 6.1 μg/mL). Because of the potential clinical utility of anaephene B, investigation into synthetic production was warranted. A convergent synthesi...
A small molecule (1835F03) that inhibits Staphylococcus aureus wall teichoic acid biosynthesis, a pr...
Library Synthesis of antimicrobial peptide targeting Staphylococcus aureus Due to the overprescribin...
Most of the known antibiotics still in use nowadays have been discovered in the 1940s–1960s by exten...
As strains of bacteria continuously evolve and become resistant to modern antibiotics, there exists ...
Staphylococcus aureusand methicillin-resistantStaphylococcus aureus(MRSA) have become serious infect...
The Gram positive, cluster forming bacteria Staphylococcus aureus belongs to the family of opportuni...
Staphylococcus aureus is a major cause of nosocomial infections and secretes a diverse spectrum of v...
Nosocomial and community-acquired infections caused by multidrug resistant bacteria represent a majo...
An efficient synthesis of two new N-acetyl-4’-arylphenylalanines is described together with their in...
This is the published version. Copyright Royal Society of ChemistryA chemically diverse library of T...
Nosocomial and community-acquired infections caused by multidrug resistant bacteria represent a majo...
The synthesis of eleven novel antibacterial agents is reported. The structures are based on a C2-sym...
We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[d]thiazol-2-ylthio)-...
This thesis details research in three areas, in attempts to produce more effective inhibitors of the...
Development of antimicrobial agents that work through novel mechanisms is of importance for combatin...
A small molecule (1835F03) that inhibits Staphylococcus aureus wall teichoic acid biosynthesis, a pr...
Library Synthesis of antimicrobial peptide targeting Staphylococcus aureus Due to the overprescribin...
Most of the known antibiotics still in use nowadays have been discovered in the 1940s–1960s by exten...
As strains of bacteria continuously evolve and become resistant to modern antibiotics, there exists ...
Staphylococcus aureusand methicillin-resistantStaphylococcus aureus(MRSA) have become serious infect...
The Gram positive, cluster forming bacteria Staphylococcus aureus belongs to the family of opportuni...
Staphylococcus aureus is a major cause of nosocomial infections and secretes a diverse spectrum of v...
Nosocomial and community-acquired infections caused by multidrug resistant bacteria represent a majo...
An efficient synthesis of two new N-acetyl-4’-arylphenylalanines is described together with their in...
This is the published version. Copyright Royal Society of ChemistryA chemically diverse library of T...
Nosocomial and community-acquired infections caused by multidrug resistant bacteria represent a majo...
The synthesis of eleven novel antibacterial agents is reported. The structures are based on a C2-sym...
We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[d]thiazol-2-ylthio)-...
This thesis details research in three areas, in attempts to produce more effective inhibitors of the...
Development of antimicrobial agents that work through novel mechanisms is of importance for combatin...
A small molecule (1835F03) that inhibits Staphylococcus aureus wall teichoic acid biosynthesis, a pr...
Library Synthesis of antimicrobial peptide targeting Staphylococcus aureus Due to the overprescribin...
Most of the known antibiotics still in use nowadays have been discovered in the 1940s–1960s by exten...