[HTML][HTML] DNA topoisomerase I and DNA gyrase as targets for TB therapy

V Nagaraja, AA Godbole, SR Henderson… - Drug discovery today, 2017 - Elsevier
Highlights•DNA topoisomerases are key targets for antibacterial and anticancer
chemotherapy.•TB topo I is validated as an antibacterial target.•Inhibitors that target TB topo I …

Indole derivatives as anti-tubercular agents: An overview on their synthesis and biological activities

GS Reddy, M Pal - Current Medicinal Chemistry, 2021 - ingentaconnect.com
Background: The indole framework is considered as one of the privileged structures in the
area of medicinal chemistry and drug discovery because compounds containing this …

Design, synthesis and 2D QSAR study of novel pyridine and quinolone hydrazone derivatives as potential antimicrobial and antitubercular agents

MA Abdelrahman, I Salama, MS Gomaa… - European Journal of …, 2017 - Elsevier
The increased development of highly resistant bacterial strains and tuberculosis, constitute a
serious public health threat, highlighting the urgent need of novel antibacterial agents. In this …

Mycobacterium Tuberculosis (MTB) GyrB inhibitors: An attractive approach for developing novel drugs against TB

K Chaudhari, S Surana, P Jain, HM Patel - European journal of medicinal …, 2016 - Elsevier
New classes of drugs are needed to treat tuberculosis (TB) in order to combat the
emergence of resistance (MDR and XDR) to existing agents and shorten the duration of …

Recent progress in the discovery and development of DNA gyrase B inhibitors

M Barančoková, D Kikelj, J Ilaš - Future medicinal chemistry, 2018 - Taylor & Francis
New antibacterials that modulate less explored targets are needed to fight the emerging
bacterial resistance. DNA gyrase and topoisomerase IV are attractive targets in this search …

Targeting DNA replication and repair for the development of novel therapeutics against tuberculosis

MA Reiche, DF Warner, V Mizrahi - Frontiers in molecular …, 2017 - frontiersin.org
Mycobacterium tuberculosis is the etiological agent of tuberculosis (TB), an infectious
disease which results in approximately 10 million incident cases and 1.4 million deaths …

Ligand-Based Virtual Screening for Discovery of Indole Derivatives as Potent DNA Gyrase ATPase Inhibitors Active against Mycobacterium tuberculosis and Hit …

B Pakamwong, P Thongdee, B Kamsri… - Journal of Chemical …, 2024 - ACS Publications
Mycobacterium tuberculosis is the single most important global infectious disease killer and
a World Health Organization critical priority pathogen for development of new antimicrobials …

How Mycobacterium tuberculosis drug resistance has shaped anti-tubercular drug discovery

A Bhagwat, A Deshpande, T Parish - Frontiers in Cellular and Infection …, 2022 - frontiersin.org
Drug resistance is an increasing problem for the treatment of tuberculosis. The prevalence of
clinical isolates with pre-existing resistance needs to be considered in any drug discovery …

Chemical classes targeting energy supplying GyrB domain of Mycobacterium tuberculosis

A Kashyap, PK Singh, O Silakari - Tuberculosis, 2018 - Elsevier
Tuberculosis (TB) is contagious in nature and immunocompromised patients have a higher
probability of developing TB. The occurrence of drug resistance, has led to serious health …

Development of acridine derivatives as selective Mycobacterium tuberculosis DNA gyrase inhibitors

B Medapi, N Meda, P Kulkarni, P Yogeeswari… - Bioorganic & medicinal …, 2016 - Elsevier
In this study we have designed p-phenylene diamine linked acridine derivative from our
earlier reported quinoline–aminopiperidine hybrid MTB DNA gyrase inhibitors with aiming …