[HTML][HTML] Phytochemicals: a promising weapon in the arsenal against antibiotic-resistant bacteria

B Khameneh, NAM Eskin, M Iranshahy… - Antibiotics, 2021 - mdpi.com
The extensive usage of antibiotics and the rapid emergence of antimicrobial-resistant
microbes (AMR) are becoming important global public health issues. Many solutions to …

Recent advances of imidazole-containing derivatives as anti-tubercular agents

YL Fan, XH Jin, ZP Huang, HF Yu, ZG Zeng… - European journal of …, 2018 - Elsevier
Tuberculosis still remains one of the most common, communicable, and leading deadliest
diseases known to mankind throughout the world. Drug-resistance in Mycobacterium …

Antibacterial activity of quinoxalines, quinazolines, and 1, 5-naphthyridines

AK Parhi, Y Zhang, KW Saionz, P Pradhan… - Bioorganic & medicinal …, 2013 - Elsevier
Several phenyl substituted naphthalenes and isoquinolines have been identified as
antibacterial agents that inhibit FtsZ-Zing formation. In the present study we evaluated the …

Targeting the bacterial division protein FtsZ

KA Hurley, TMA Santos, GM Nepomuceno… - Journal of medicinal …, 2016 - ACS Publications
Similar to its eukaryotic counterpart, the prokaryotic cytoskeleton is essential for the
structural and mechanical properties of bacterial cells. The essential protein FtsZ is a central …

[HTML][HTML] Tackling multiple-drug-resistant bacteria with conventional and complex phytochemicals

T Suganya, IASV Packiavathy… - Frontiers in Cellular …, 2022 - frontiersin.org
Emerging antibiotic resistance in bacteria endorses the failure of existing drugs with chronic
illness, complicated treatment, and ever-increasing expenditures. Bacteria acquire the …

TXA709, an FtsZ-Targeting Benzamide Prodrug with Improved Pharmacokinetics and Enhanced In Vivo Efficacy against Methicillin-Resistant Staphylococcus aureus

M Kaul, L Mark, Y Zhang, AK Parhi, YL Lyu… - Antimicrobial agents …, 2015 - Am Soc Microbiol
The clinical development of FtsZ-targeting benzamide compounds like PC190723 has been
limited by poor drug-like and pharmacokinetic properties. Development of prodrugs of …

Mechanism of action of the cell-division inhibitor PC190723: modulation of FtsZ assembly cooperativity

NL Elsen, J Lu, G Parthasarathy, JC Reid… - Journal of the …, 2012 - ACS Publications
The cooperative assembly of FtsZ, the prokaryotic homologue of tubulin, plays an essential
role in cell division. FtsZ is a potential drug target, as illustrated by the small-molecule cell …

Targeting the assembly of bacterial cell division protein FtsZ with small molecules

C Schaffner-Barbero, M Martín-Fontecha… - ACS chemical …, 2012 - ACS Publications
FtsZ is the key protein of bacterial cell division and an emergent target for new antibiotics. It
is a filament-forming GTPase and a structural homologue of eukaryotic tubulin. A number of …

Ruthenium-Catalyzed Redox-Neutral C–H Activation via N–N Cleavage: Synthesis of N-Substituted Indoles

Z Zhang, H Jiang, Y Huang - Organic letters, 2014 - ACS Publications
The first Ru-catalyzed redox-neutral C–H activation reaction via N–N bond cleavage is
reported. Pyrazolidin-3-one is demonstrated as an internally oxidative directing group that …

An Improved Small-Molecule Inhibitor of FtsZ with Superior In Vitro Potency, Drug-Like Properties, and In Vivo Efficacy

NR Stokes, N Baker, JM Bennett, J Berry… - Antimicrobial agents …, 2013 - Am Soc Microbiol
The bacterial cell division protein FtsZ is an attractive target for small-molecule antibacterial
drug discovery. Derivatives of 3-methoxybenzamide, including compound PC190723, have …