Development of the diaryl ether scaffold as inhibitors of EcDsbA using a fragment-based approach
MATTHEW ROSS BENTLEY
10.26180/5eb8df81e0487
https://bridges.monash.edu/articles/thesis/Development_of_the_diaryl_ether_scaffold_as_inhibitors_of_EcDsbA_using_a_fragment-based_approach/12279554
Antibiotic resistance is becoming a global health threat and drugs with novel mechanisms of action are required to provide new approaches to the treatment of bacterial infections and to combat resistance. This thesis examines the development of a series of novel anti-bacterial compounds targeting the bacterial enzyme DsbA. DsbA is required for the correct folding of many proteins that the bacteria use to establish an infection. Inhibitors of DsbA have the potential to “disarm” bacteria and thereby render them avirulent. As such DsbA inhibitors would represent a novel therapeutic approach to the treatment of bacterial infections.
2020-05-11 05:15:44
Medicinal chemistry
Fragment based drug discovery
Pharmaceutical Sciences