1, 2, 3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA)

Z Xu - European journal of medicinal chemistry, 2020 - Elsevier
Methicillin-resistant Staphylococcus aureus (MRSA), as a classic reason for genuine skin
and flimsy tissues diseases, is a worldwide general wellbeing risk and has already …

Oxazolidinones as versatile scaffolds in medicinal chemistry

GFS Fernandes, CB Scarim, SH Kim, J Wu… - RSC Medicinal …, 2023 - pubs.rsc.org
Oxazolidinone is a five-member heterocyclic ring with several biological applications in
medicinal chemistry. Among the three possible isomers, 2-oxazolidinone is the most …

The current status of O‐heterocycles: A synthetic and medicinal overview

PK Singh, O Silakari - ChemMedChem, 2018 - Wiley Online Library
O‐Heterocycles have been explored in the field of medicinal chemistry for a long time, but
their significance has not been duly recognised and they are often shunned in favour of N …

Oxazolidinones as anti-tubercular agents: discovery, development and future perspectives

PS Jadhavar, MD Vaja, TM Dhameliya… - Current medicinal …, 2015 - ingentaconnect.com
TB drug development pipeline represents varied structural classes of molecules.
Oxazolidinones represent synthetic anti-bacterial agents with unique mechanism of action …

Recent advances in oxazolidinones as antituberculosis agents

H Lu, H Wang, H Zhao, D Zhang - Future Medicinal Chemistry, 2022 - Taylor & Francis
Tuberculosis (TB) is an infectious and fatal disease caused by Mycobacterium tuberculosis
(Mtb) and remains a serious public health threat; therefore, the development of new …

Structural toxicity relationship (STR) of linezolid to mitigate myelosuppression and serotonergic toxicity

M Shaikh, H Patel - Bioorganic & Medicinal Chemistry, 2024 - Elsevier
Tuberculosis (TB) remains a significant global health challenge, with “multidrug-resistant
(MDR-TB) and extensively drug-resistant (XDR-TB) strains” posing severe threats to …

Synthesis and biological evaluation of pyrimidine-oxazolidin-2-arylimino hybrid molecules as antibacterial agents

R Romeo, MA Chiacchio, A Campisi, G Monciino… - Molecules, 2018 - mdpi.com
Pyrimidine-1, 3-oxazolidin-2-arylimino hybrids have been synthesized as a new class of
antibacterial agents. The synthetic approach exploits a Cu (II)-catalyzed intramolecular …

In vitro activities of LCB 01-0648, a novel oxazolidinone, against gram-positive bacteria

SH Oh, J Kim, SY Baek, SE Chae, HS Park, YL Cho… - Molecules, 2017 - mdpi.com
Oxazolidinones are a novel class of synthetic antibacterial agents that inhibit bacterial
protein synthesis. Here, we synthesized and tested a series of oxazolidinone compounds …

[PDF][PDF] Molecular modelling and machine learning for the investigation of 2-oxazolidinone ribosomal antibacterials

MK Buckley - 2023 - eprints.qut.edu.au
This thesis by publication compares computational methods to analyze an untested dataset
of oxazolidinones, a type of antibacterials that target ribosomes. The study evaluates …

Selective octahydro-cyclopenta [C] pyrrole negative modulators of NR2B

DR Anderson, RA Volkmann, FS Menniti - US Patent 10,052,306, 2018 - Google Patents
US10052306B2 - Selective octahydro-cyclopenta[C] pyrrole negative modulators of NR2B -
Google Patents US10052306B2 - Selective octahydro-cyclopenta[C] pyrrole negative …