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Naphthoylhydrazones: coordination to metal ions and biological screening

Authors :
Adelino M. Galvão
Rute Pinheiro
Patrícia Rijo
Helena Ramos
Isabel Cavaco
Lucília Saraiva
Isabel Correia
Nádia Ribeiro
Filipa Ramilo-Gomes
Epole Ntungwe
Clara S. B. Gomes
Vera M. S. Isca
Rita C. Guedes
João Costa Pessoa
Source :
Repositório Científico de Acesso Aberto de Portugal, Repositório Científico de Acesso Aberto de Portugal (RCAAP), instacron:RCAAP
Publication Year :
2019
Publisher :
Royal Society of Chemistry (RSC), 2019.

Abstract

We report the synthesis of 3-hydroxyl-2-naphthoylhydrazones containing pyrrole (HL1), furane (HL2) and thiophene (HL3) moieties and their V(IV)O-, Cu(II)- and Zn(II)-complexes. All compounds are characterized by the usual analytical techniques and coordination of the ligands to the metal ions is discussed based on spectroscopic data (FTIR, UV-vis, EPR and NMR) as well as CAMB3LYP DFT/TDDFT calculations, indicating the formation of neutral ML2 type complexes. The photophysical properties of ligands and complexes are disclosed. The binding to Bovine Serum Albumin (BSA) is evaluated in detail using several spectroscopic tools. Circular dichroism shows that the compounds, and particularly the ligand precursors, stabilize BSA, increasing its a-helical content. Fluorescence studies indicate the formation of 1 : 1 protein-compound adducts, which is corroborated by molecular docking studies that show the interaction between Trp 213 of BSA and the naphthalene rings. The general toxicity is evaluated using the Artemia salina lethality assay, with all compounds showing general toxicity towards the brine shrimp model. The cytotoxicity on human cancer cells (H1299, MCF7, and HCT116) is assessed for all compounds and the half-maximal inhibitory concentration (IC50) values are in the range from 0.57 to 27.35 mu M. Compounds containing L-1 (pyrrole derivative) are the most cytotoxic, with the vanadium and zinc complexes performing better than the copper ones, and some of them depicting IC50 values lower than 1.1 mM. However, selectivity needs improvement as the compounds show toxicity towards Artemia salina and normal fibroblasts. Fundacao para a Ciencia e a Tecnologia (FCT)Portuguese Foundation for Science and Technology [UID/QUI/00100/2019, UID/MULTI/04349/2013, UID/BIO/04565/2013, RECI/QEQ-QIN/0189/2012, RECI/QEQ-MED/0330/2012, UID/DTP/04567/2016] Programa Operacional Regional de Lisboa [LISBOA-01-0145-FEDER-007317] [UID/04138/2019] [SAICTPAC/0019/2015] [PTDC/QUI-QAN/32242/2017] [PD/BD/128320/2017] [SFRH/BD/135797/2018] [SFRH/BPD/107834/2015] [UID/QUI/50006/2019] [RECI/BBB-BEP/0124/2012] [UID/DTP/04567/2019] [SFRH/BD/119144/2016] info:eu-repo/semantics/publishedVersion

Details

ISSN :
13699261 and 11440546
Volume :
43
Database :
OpenAIRE
Journal :
New Journal of Chemistry
Accession number :
edsair.doi.dedup.....9861d315b7a0133764eac61207151483
Full Text :
https://doi.org/10.1039/c9nj01816f