Breaking down the cell wall: Still an attractive antibacterial strategy

J Zhou, Y Cai, Y Liu, H An, K Deng, MA Ashraf… - Frontiers in …, 2022 - frontiersin.org
Since the advent of penicillin, humans have known about and explored the phenomenon of
bacterial inhibition via antibiotics. However, with changes in the global environment and the …

A comprehensive survey of small-molecule binding pockets in proteins

M Gao, J Skolnick - PLoS computational biology, 2013 - journals.plos.org
Many biological activities originate from interactions between small-molecule ligands and
their protein targets. A detailed structural and physico-chemical characterization of these …

The biology of Mur ligases as an antibacterial target

I Kouidmi, RC Levesque… - Molecular …, 2014 - Wiley Online Library
With antibiotic resistance mechanisms increasing in diversity and spreading among
bacterial pathogens, the development of new classes of antibacterial agents against …

Sulfonyl group-containing compounds in the design of potential drugs for the treatment of diabetes and its complications

X Chen, S Hussain, S Parveen, S Zhang… - Current medicinal …, 2012 - ingentaconnect.com
Sulfonyl group-containing compounds constitute an important class of therapeutical agents
in medicinal chemistry presumably because of the tense chemical structure and functionality …

Inhibitors of the peptidoglycan biosynthesis enzymes MurA-F

M Hrast, I Sosič, R Šink, S Gobec - Bioorganic chemistry, 2014 - Elsevier
The widespread emergence of resistant bacterial strains is becoming a serious threat to
public health. This thus signifies the need for the development of new antibacterial agents …

Strategies in the rational drug design

T Mavromoustakos, S Durdagi… - Current medicinal …, 2011 - ingentaconnect.com
Rational design is applied in the discovery of novel lead drugs. Its rapid development is
mainly attributed to the tremendous advancements in the computer science, statistics …

Amino acid based antimicrobial agents–synthesis and properties

MG Nowak, AS Skwarecki, MJ Milewska - ChemMedChem, 2021 - Wiley Online Library
Structures of several dozen of known antibacterial, antifungal or antiprotozoal agents are
based on the amino acid scaffold. In most of them, the amino acid skeleton is of a crucial …

Discovery of novel 5-benzylidenerhodanine and 5-benzylidenethiazolidine-2, 4-dione inhibitors of MurD ligase

N Zidar, T Tomašić, R Šink, V Rupnik… - Journal of medicinal …, 2010 - ACS Publications
We have designed, synthesized, and evaluated 5-benzylidenerhodanine-and 5-
benzylidenethiazolidine-2, 4-dione-based compounds as inhibitors of bacterial enzyme …

Selective Late‐Stage Sulfonyl Chloride Formation from Sulfonamides Enabled by Pyry‐BF4

A Gómez‐Palomino, J Cornella - Angewandte Chemie, 2019 - Wiley Online Library
Reported here is a simple and practical functionalization of primary sulfonamides, by means
of a pyrylium salt (Pyry‐BF4), with nucleophiles. This simple reagent activates the poorly …

Peptidoglycan biosynthesis machinery: a rich source of drug targets

A Gautam, R Vyas, R Tewari - Critical reviews in biotechnology, 2011 - Taylor & Francis
The range of antibiotic therapy for the control of bacterial infections is becoming increasingly
limited because of the rapid rise in multidrug resistance in clinical bacterial isolates. A few …