A conceptual review of rhodanine: current applications of antiviral drugs, anticancer and antimicrobial activities

SM Mousavi, M Zarei, SA Hashemi… - Artificial cells …, 2019 - Taylor & Francis
Rhodanines are accepted as advantaged heterocycles in medicinal chemistry as one of the
4-thiazolidinones subtypes. The aim of this paper is to analyze the features of rhodanine and …

Looking beyond typical treatments for atypical mycobacteria

CM Bento, MS Gomes, T Silva - Antibiotics, 2020 - mdpi.com
The genus Mycobacterium comprises not only the deadliest of bacterial pathogens,
Mycobacterium tuberculosis, but several other pathogenic species, including M. avium and …

Repurposing Salicylanilide Anthelmintic Drugs to Combat Drug Resistant Staphylococcus aureus

R Rajamuthiah, BB Fuchs, AL Conery, W Kim… - PloS one, 2015 - journals.plos.org
Staphylococcus aureus is a Gram-positive bacterium that has become the leading cause of
hospital acquired infections in the US. Repurposing Food and Drug Administration (FDA) …

Synthesis and biological evolution of hydrazones derived from 4-(trifluoromethyl) benzohydrazide

M Krátký, S Bősze, Z Baranyai, J Stolaříková… - Bioorganic & medicinal …, 2017 - Elsevier
Reflecting the known biological activity of isoniazid-based hydrazones, seventeen
hydrazones of 4-(trifluoromethyl) benzohydrazide as their bioisosters were synthesized from …

Antimicrobial activity of rhodanine-3-acetic acid derivatives

M Krátký, J Vinšová, J Stolaříková - Bioorganic & Medicinal Chemistry, 2017 - Elsevier
Abstract Twenty-four 2-(4-oxo-2-thioxothiazolidin-3-yl) acetic acid (rhodanine-3-acetic acid)-
based amides, esters and 5-arylalkylidene derivatives were synthesized, characterized and …

Host cell targeting of novel antimycobacterial 4-aminosalicylic acid derivatives with tuftsin carrier peptides

LB Horváth, M Krátký, V Pflégr, E Méhes… - European Journal of …, 2022 - Elsevier
Mycobacterium tuberculosis is an intracellular pathogen and the uptake of the
antimycobacterial compounds by host cells is limited. Novel antimycobacterials effective …

Synthesis and antimycobacterial properties of ring-substituted 6-hydroxynaphthalene-2-carboxanilides

J Kos, E Nevin, M Soral, I Kushkevych, T Gonec… - Bioorganic & medicinal …, 2015 - Elsevier
In this study, a series of twenty-two ring-substituted 6-hydroxynaphthalene-2-carboxanilides
was prepared and characterized. Primary in vitro screening of the synthesized compounds …

Salicylanilide N-monosubstituted carbamates: Synthesis and in vitro antimicrobial activity

M Krátký, J Vinšová - Bioorganic & medicinal chemistry, 2016 - Elsevier
The research of innovative antimicrobial agents represents a cutting edge topic. Hence, we
synthesized and characterised novel salicylanilide N-monosubstituted carbamates. Twenty …

Novel salicylanilides from 4, 5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity

G Paraskevopoulos, S Monteiro, R Vosátka… - Bioorganic & medicinal …, 2017 - Elsevier
Salicylanilides have proved their activity against tuberculosis (TB). One weak electron-
withdrawing substituent is favored at the salicylic part, specially Cl or Br atoms at positions 4 …

Phenolic N-monosubstituted carbamates: Antitubercular and toxicity evaluation of multi-targeting compounds

M Krátký, O Janďourek, Z Baranyai, E Novotna… - European Journal of …, 2019 - Elsevier
The research of novel antimycobacterial drugs represents a cutting-edge topic. Thirty
phenolic N-monosubstituted carbamates, derivatives of salicylanilides and 4-chlorophenol …