Triazole derivatives and their anti-tubercular activity

S Zhang, Z Xu, C Gao, QC Ren, L Chang, ZS Lv… - European journal of …, 2017 - Elsevier
Tuberculosis (TB) remains one of the most widespread and leading deadliest diseases,
threats one-third of the world's population. Although numerous efforts have been undertaken …

Bacterial fatty acid metabolism in modern antibiotic discovery

J Yao, CO Rock - Biochimica et Biophysica Acta (BBA)-Molecular and …, 2017 - Elsevier
Bacterial fatty acid synthesis is essential for many pathogens and different from the
mammalian counterpart. These features make bacterial fatty acid synthesis a desirable …

Anti-Tubercular Properties of 4-Amino-5-(4-Fluoro-3- Phenoxyphenyl)-4H-1,2,4-Triazole-3-Thiol and Its Schiff Bases: Computational Input and Molecular Dynamics

KN Venugopala, M Kandeel, M Pillay, PK Deb… - Antibiotics, 2020 - mdpi.com
In the present investigation, the parent compound 4-amino-5-(4-fluoro-3-phenoxyphenyl)-4
H-1, 2, 4-triazole-3-thiol (1) and its Schiff bases 2, 3, and 4 were subjected to whole-cell anti …

An integrative, multi-omics approach towards the prioritization of Klebsiella pneumoniae drug targets

PIP Ramos, D Fernandez Do Porto, E Lanzarotti… - Scientific reports, 2018 - nature.com
Klebsiella pneumoniae (Kp) is a globally disseminated opportunistic pathogen that can
cause life-threatening infections. It has been found as the culprit of many infection outbreaks …

Mycobacterium tuberculosis KasA as a drug target: Structure-based inhibitor design

RS Rudraraju, SS Daher, R Gallardo-Macias… - Frontiers in Cellular …, 2022 - frontiersin.org
Recent studies have reported the β-ketoacyl-acyl carrier protein KasA as a druggable target
for Mycobacterium tuberculosis. This review summarizes the current status of major classes …

Combating antimicrobial resistance in the post-genomic era: rapid antibiotic discovery

Y Yang, MGC Kessler, MR Marchán-Rivadeneira… - Molecules, 2023 - mdpi.com
Constantly evolving drug-resistant “superbugs” have caused an urgent demand for novel
antimicrobial agents. Natural products and their analogs have been a prolific source of …

Design, synthesis, and in vitro biological evaluation of novel benzimidazole tethered allylidenehydrazinylmethylthiazole derivatives as potent inhibitors of …

G Surineni, Y Gao, M Hussain, Z Liu, Z Lu… - …, 2019 - pubs.rsc.org
Tuberculosis (TB) has become one of the most significant public health problems in recent
years. Antibiotic therapy remains the mainstay of TB control strategies, but the increasing …

Detectives and helpers: Natural products as resources for chemical probes and compound libraries

A Parthasarathy, PK Mantravadi, K Kalesh - Pharmacology & Therapeutics, 2020 - Elsevier
About 70% of the drugs in use are derived from natural products, either used directly or in
chemically modified form. Among all possible small molecules (not greater than 5 kDa), only …

Chemical highlights supporting the role of lipid A in efficient biological adaptation of gram-negative bacteria to external stresses

A Troudi, JM Pagès, JM Brunel - Journal of Medicinal Chemistry, 2021 - ACS Publications
The outer membrane (OM) of Gram-negative bacteria provides an efficient barrier against
external noxious compounds such as antimicrobial agents. Associated with drug target …

Emerging role of biologics for the treatment of melioidosis and glanders

D Tapia, JI Sanchez-Villamil… - Expert opinion on …, 2019 - Taylor & Francis
Introduction: Two important pathogenic species within the genus Burkholderia, namely
Burkholderia pseudomallei (Bpm) and Burkholderia mallei (Bm), are the causative agents of …