[HTML][HTML] Modifications of quinolones and fluoroquinolones: hybrid compounds and dual-action molecules

J Fedorowicz, J Sączewski - Monatshefte für Chemie-Chemical Monthly, 2018 - Springer
This review is aimed to provide extensive survey of quinolones and fluoroquinolones for a
variety of applications ranging from metal complexes and nanoparticle development to …

Development of new antituberculosis drugs among of 1, 3-and 1, 4-diazines. Highlights and perspectives

EV Verbitskiy, GL Rusinov, VN Charushin… - Russian Chemical …, 2019 - Springer
The properties of pyrimidine and pyrazine derivatives responsible for the existence of
antituberculosis activity are considered. Examples of synthesis and biological activity of the …

The bioisosteric modification of pyrazinamide derivatives led to potent antitubercular agents: Synthesis via click approach and molecular docking of pyrazine-1, 2, 3 …

R Reddyrajula, U Dalimba - Bioorganic & Medicinal Chemistry Letters, 2020 - Elsevier
Tuberculosis remains as a major public health risk which causes the highest mortality rate
globally and an improved regimen is required to treat the drug-resistant strains …

Synthesis and molecular modeling of antimicrobial active fluoroquinolone–pyrazine conjugates with amino acid linkers

SS Panda, OS Detistov, AS Girgis… - Bioorganic & Medicinal …, 2016 - Elsevier
Novel fluoroquinolone–pyrazine conjugates 7a–h with amino acid linkers were synthesized
in good yields utilizing benzotriazole chemistry. Antimicrobial bioassay showed that the …

[HTML][HTML] Synthesis, and biological screening of chloropyrazine conjugated benzothiazepine derivatives as potential antimicrobial, antitubercular and cytotoxic agents

AB Shaik, RR Bhandare, S Nissankararao… - Arabian Journal of …, 2021 - Elsevier
A series of twenty new chloropyrazine conjugated benzothiazepines (22–41) have been
synthesized with 58%–95% yields. The compounds were characterized by using different …

Spectroscopic, quantum chemical studies, Fukui functions, in vitro antiviral activity and molecular docking of 5-chloro-N-(3-nitrophenyl) pyrazine-2-carboxamide

SHR Sebastian, MA Al-Alshaikh, AA El-Emam… - Journal of Molecular …, 2016 - Elsevier
The molecular structural parameters and vibrational frequencies of 5-chloro-N-(3-
nitrophenyl) pyrazine-2-carboxamide have been obtained using density functional theory …

Spectroscopic and theoretical characterization of 2-(4-methoxyphenyl)-4, 5-dimethyl-1H-imidazole 3-oxide

KB Benzon, HT Varghese, CY Panicker… - … Acta Part A: Molecular …, 2015 - Elsevier
The optimized molecular structure, vibrational frequencies, corresponding vibrational
assignments of 2-(4-methoxyphenyl)-4, 5-dimethyl-1H-imidazole 3-oxide have been …

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 …

[HTML][HTML] Synthesis of novel pyrazinamide derivatives based on 3-chloropyrazine-2-carboxamide and their antimicrobial evaluation

O Jandourek, M Tauchman, P Paterova, K Konecna… - Molecules, 2017 - mdpi.com
Aminodehalogenation of 3-chloropyrazine-2-carboxamide with variously substituted
benzylamines yielded a series of fifteen 3-benzylaminopyrazine-2-carboxamides. Four …

[HTML][HTML] Synthesis, Antimycobacterial Activity and In Vitro Cytotoxicity of 5-Chloro-N-phenylpyrazine-2-carboxamides

J Zitko, B Servusová, P Paterová, J Mandíková… - Molecules, 2013 - mdpi.com
5-Chloropyrazinamide (5-Cl-PZA) is an inhibitor of mycobacterial fatty acid synthase I with a
broad spectrum of antimycobacterial activity in vitro. Some N-phenylpyrazine-2 …