Artículo

Anti-thyroid and antifungal activities, BSA interaction and acid phosphatase inhibition of methimazole copper(II) complexes

Urquiza, Nora María ; Islas, María Soledad Icon; Ariza, Santiago T. ; Jori, Nadir ; Martínez Medina, Juan José Icon; Lavecchia, Martín José Icon; López Tévez, Libertad Leonor ; Lezama, Luis ; Rojo, Teófilo ; Williams, Patricia Ana María ; Ferrer, Evelina Gloria Icon

Otros responsables

Fecha

03/2015

Editorial

Elsevier Ireland

Revista

Chemico-biological Interactions

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0009-2797

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

It has been reported that various metal coordination compounds have improved some biological properties. A high activity of acid phosphatase (AcP) is associated to several diseases (osteoporosis, Alzheimer's, prostate cancer, among others) and makes it a target for the development of new potential inhibitors. Anti-thyroid agents have disadvantageous side effects and the scarcity of medicines in this area motivated many researchers to synthesize new ones. Several copper(II) complexes have shown antifungal activities. In this work we presented for a first time the inhibition of AcP and the anti-thyroid activity produced by methimazole-Cu(II) complexes. Cu-Met ([Cu(MeimzH)2(H2O)2](NO3)2·H2O) produces a weak inhibition action while Cu-Met-phen ([Cu(MeimzH)2(phen)(H2O)2]Cl2) shows a strong inhibition effect (IC50 = 300 μM) being more effective than the reported behavior of vanadium complexes. Cu-Met-phen also presented a fairly good anti-thyroid activity with a formation constant value, Kc = 1.02 × 1010 M-1 being 106 times more active than methimazole (Kc = 4.16 × 104 M-1) in opposition to Cu-Met which presented activity (Kc = 9.54 × 103 M-1) but in a lesser extent than that of the free ligand. None of the complexes show antifungal activity except Cu-phen (MIC = 11.71 μg mL-1 on Candida albicans) which was tested for comparison. Besides, albumin interaction experiments denoted high affinity toward the complexes and the calculated binding constants indicate reversible binding to the protein.

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