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New silver(I) phosphino complexes: Evaluation of their potential as prospective agents against Mycobacterium tuberculosis

Authors :
Yndira Dolores Maldonado
Gonzalo Scalese
Karyn Fernanda Manieri
Fernando R. Pavan
Larry D. Aguirre Méndez
Dinorah Gambino
Universidad Nacional de Ingeniería
Universidad de la República
Universidade Estadual Paulista (UNESP)
Source :
Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP
Publication Year :
2022

Abstract

Made available in DSpace on 2022-05-01T11:07:40Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-02-01 Despite being a preventable and curable disease, Tuberculosis (TB) is the world's top infectious killer. Development of new drugs is urgently needed. In this work, the synthesis and characterization of new silver(I) complexes, that include N′-[(E)-(pyridine-2-ylmethylene)pyrazine-2-carbohydrazide, HPCPH, as main ligand and substituted aryl-phosphines as auxiliary ligands, is reported. HPCPH was synthesized from pyrazinoic acid, the active metabolite of the first-line antimycobacterial drug pyrazinamide. Complexes [Ag(HPCPH)(PPh3)2]OTf (1), [Ag(HPCPH)((P(p-tolyl)3)2]OTf (2) and [Ag(HPCPH)(P(p-anisyl)3)2]OTf (3) were characterized in solid state and in solution by elemental analysis and FTIR and NMR spectroscopies (OTf[dbnd]triflate). Crystal structures of (1,2) were determined by XRD. The Ag atom is coordinated to azomethine and pyridine nitrogen atoms of HPCPH ligand and to the phosphorous atom of each aryl-phosphine co-ligand. Although HPCPH did not show activity, the Ag(I) compounds demonstrated activity against Mycobacterium tuberculosis (MTB), H37Rv strain, and multi-drug resistant clinical isolates (MDR-TB). Globally, results showed that the compounds are not only effective against the sensitive strain, but are more potent against MDR-TB than antimycobacterial drugs used in therapy. The compounds showed low to moderate selectivity index values (SI) towards the bacteria, using MRC-5 cells (ATCC CCL-171) as mammalian cell model. Interaction with DNA was explored to get insight into the potential mechanism of action against the pathogen. No significant interaction was detected, allowing to discard this biomolecule as a potential molecular target. Compound 1 was identified as a hit compound (MIC90 2.23 μM; SI 4.4) to develop further chemical modifications in the search for new drugs. Escuela de Ingeniería Química Facultad de Ingeniería Química y Textil Universidad Nacional de Ingeniería Laboratorio de Biopolímeros y Metalofármacos LIBIPMET Facultad de Ciencias Universidad Nacional de Ingeniería Área Química Inorgánica Facultad de Química Universidad de la República Faculdade de Ciências Farmacêuticas UNESP Facultad de Ingeniería Eléctrica y Electrónica Universidad Nacional de Ingeniería Faculdade de Ciências Farmacêuticas UNESP

Details

Language :
English
Database :
OpenAIRE
Journal :
Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP
Accession number :
edsair.doi.dedup.....8e1efc6455b1ab50c7908067ade55df1