Electrochemistry of ring-substituted 1-hydroxynaphthalene-2-carboxanilides: Relation to structure and biological activity

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:2981039 25 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Electrochemistry of ring-substituted 1-hydroxynaphthalene-2-carboxanilides: Relation to structure and biological activity
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Twenty-two novel antimycobacterial agents, 1-hydroxynaphthalene-2-carboxanilides, were studied by cyclic voltammetry on a glassy carbon electrode in a phosphate buffer pH 7.2 – dimethyl sulfoxide (DMSO) mixed medium (9:1; v/v). All compounds exhibited similar voltammetric behavior with one irreversible anodic signal in the range 100–300 mV corresponding to the oxidation of hydroxyl group on the naphthalene moiety. A shift of the oxidation potential was caused solely by electron donating or withdrawing effects of substituents and their position on the benzene moiety. Mechanism of oxidation in the studied medium was briefly outlined. Values of oxidation potentials exhibited very good linear correlation with calculated Hammett σ substituent constants. For all active compounds, a relationship between oxidation potentials and MIC or IC50 values obtained from in vitro screening was investigated in detail. Primary in vitro screening of synthesized compounds was previously performed against three species of Mycobacterium pathogens. Additionally, their activity related to the inhibition of photosynthetic electron transport (PET) in spinach chloroplasts was tested in previous publications. In vitro screening against Mycobacterium tuberculosis was performed here for the first time with 1-hydroxy-N-(3-trifluoromethylphenyl)naphthalene-2-carboxamide being the most effective (MIC = 11.7 μmol L−1). Furthermore, several other compounds showed higher antimycobacterial activity than the standard isoniazid. Relation of biological activities and oxidation potentials was successfully found in some cases; however, final correlations must also be considered with other physical and chemical factors contributing to the biological activity. Relation of structure, biological activity and electrochemical potential was also studied by cyclic voltammetry in cathodic area for three compounds containing reducible nitro moiety. © 2019 Elsevier Ltd
Έτος δημοσίευσης:
2020
Συγγραφείς:
Gajdár, J.
Tsami, K.
Michnová, H.
Goněc, T.
Brázdová, M.
Soldánová, Z.
Fojta, M.
Jampílek, J.
Barek, J.
Fischer, J.
Περιοδικό:
Electrochimica Acta
Εκδότης:
ELSEVIER SCIENCE LTD.
Τόμος:
332
Λέξεις-κλειδιά:
Anodic oxidation; Cyclic voltammetry; Dimethyl sulfoxide; Electron transport properties; Glass membrane electrodes; Microwave integrated circuits; Naphthalene; Organic solvents, Antimycobacterial activity; Hammett correlation; Hydroxynaphthalene-2-carboxanilides; Photosynthetic electron transport; Structure activity relationships, Bioactivity
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.electacta.2019.135485
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