Please use this identifier to cite or link to this item: https://doi.org/10.1128/AAC.02307-16
Title: Towards selective mycobacterial ClpP1P2 inhibitors with reduced activity against the human proteasome
Authors: Moreira, W 
Santhanakrishnan, S 
Ngan, G.J.Y
Low, C.B
Sangthongpitag, K
Poulsen, A 
Dymock, B.W 
Dick, T 
Keywords: 3 phenyl 1 [[2 (pyrazine 2 carboxamido) 3 (pyridin 2 yl)propanimido]propyl]boronic acid
boronic acid derivative
bortezomib
cytochrome P450
proteasome inhibitor
proteinase inhibitor
unclassified drug
antiinfective agent
bacterial protein
bortezomib
ClpP2 protein, bacteria
endopeptidase Clp
proteasome inhibitor
serine proteinase
animal experiment
animal model
antibacterial activity
Article
bacterial growth
bactericidal activity
controlled study
drug solubility
enzyme inhibition
growth inhibition
human
human cell
mouse
Mycobacterium tuberculosis
nonhuman
plasma protein binding
priority journal
animal
antagonists and inhibitors
drug design
drug effects
genetics
lung tuberculosis
microbial sensitivity test
microbiology
molecular model
Mycobacterium smegmatis
Animals
Anti-Bacterial Agents
Bacterial Proteins
Bortezomib
Drug Design
Endopeptidase Clp
Mice
Microbial Sensitivity Tests
Models, Molecular
Mycobacterium smegmatis
Mycobacterium tuberculosis
Proteasome Inhibitors
Serine Endopeptidases
Tuberculosis, Pulmonary
Issue Date: 2017
Publisher: American Society for Microbiology
Citation: Moreira, W, Santhanakrishnan, S, Ngan, G.J.Y, Low, C.B, Sangthongpitag, K, Poulsen, A, Dymock, B.W, Dick, T (2017). Towards selective mycobacterial ClpP1P2 inhibitors with reduced activity against the human proteasome. Antimicrobial Agents and Chemotherapy 61 (5) : e02307. ScholarBank@NUS Repository. https://doi.org/10.1128/AAC.02307-16
Abstract: Mycobacterium tuberculosis is responsible for the greatest number of deaths worldwide due to a bacterial agent. We recently identified bortezomib (Velcade; compound 1) as a promising antituberculosis (anti-TB) compound. We showed that compound 1 inhibits the mycobacterial caseinolytic proteases P1 and P2 (ClpP1P2) and exhibits bactericidal activity, and we established compound 1 and ClpP1P2 as an attractive lead/target couple. However, compound 1 is a human-proteasome inhibitor currently approved for cancer therapy and, as such, exhibits significant toxicity. Selective inhibition of the bacterial protease over the human proteasome is desirable in order to maintain antibacterial activity while reducing toxicity. We made use of structural data in order to design a series of dipeptidyl-boronate derivatives of compound 1. We tested these derivatives for whole-cell ClpP1P2 and human-proteasome inhibition as well as bacterial-growth inhibition and identified compounds that were up to 100-fold-less active against the human proteasome but that retained ClpP1P2 and mycobacterialgrowth inhibition as well as bactericidal potency. The lead compound, compound 58, had low micromolar ClpP1P2 and anti-M. tuberculosis activity, good aqueous solubility, no cytochrome P450 liabilities, moderate plasma protein binding, and low toxicity in two human liver cell lines, and despite high clearance in microsomes, this compound was only moderately cleared when administered intravenously or orally to mice. Higherdose oral pharmacokinetics indicated good dose linearity. Furthermore, compound 58 was inhibitory to only 11% of a panel of 62 proteases. Our work suggests that selectivity over the human proteasome can be achieved with a drug-like template while retaining potency against ClpP1P2 and, crucially, anti-M. tuberculosis activity. Copyright © 2017 American Society for Microbiology. All Rights Reserved.
Source Title: Antimicrobial Agents and Chemotherapy
URI: https://scholarbank.nus.edu.sg/handle/10635/175227
ISSN: 0066-4804
DOI: 10.1128/AAC.02307-16
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