Adipato bridged novel hexanuclear Cu(ii) and polymeric Co(ii) coordination compounds involving cooperative supramolecular assemblies and encapsulated guest water clusters in a square grid host: antiproliferative evaluation and theoretical studies.


Journal

Dalton transactions (Cambridge, England : 2003)
ISSN: 1477-9234
Titre abrégé: Dalton Trans
Pays: England
ID NLM: 101176026

Informations de publication

Date de publication:
21 Jul 2020
Historique:
pubmed: 9 7 2020
medline: 29 4 2021
entrez: 9 7 2020
Statut: ppublish

Résumé

Two new coordination compounds involving hexanuclear Cu(ii), viz., [Cu6(phen)6(μ4-adpt)4(H2O)2](NO3)4·10H2O (1) and polymeric Co(ii), viz., {[(μ2-adpt)4Co(μ2-H2O)2Co(H2O)4]·4H2O}n (2) (phen = 1,10-phenanthroline; adpt = adipate) have been synthesized and characterized using elemental analysis, TGA, spectroscopic (IR, electronic and ESR), PXRD and single crystal X-ray diffraction techniques. Discrete nitrate-water clusters involving the [(H2O)3NO3]- core in 1 and linear (H2O)4 core in 2 provide stability to the layered network of the structures of the compounds. Interestingly, the water clusters in polymer 2 are encapsulated as guests in the voids of the host square grid that extends in 2D architecture. Theoretical studies have revealed the presence of interesting energetically significant cooperativity effects of π-stacking contacts that are responsible for the hexanuclear structure of compound 1. Both complexes significantly inhibit cell viability by inducing apoptotic cell death in the DL cancer cell line with negligible cytotoxicity in normal cells (PBMC). An assessment of ROS (reactive oxygen species) level study revealed a rapid increase of ROS in DL cells indicating cytotoxicity of the compounds against the DL cells. A decrease in MMP (mitochondrial membrane potential) is associated with an opening of the mitochondrial permeability transition pores which corroborates the apoptotic features of 1 and 2. The mode of action of the cytotoxic activities of the compounds has been explored with respect to their in silico docking ability and further inhibition of antiapoptotic proteins as evidenced by western blot analysis. SAR analyses based on pharmacophore modelling reveal that the molecular features of the structures of the compounds play important roles in biological activities.

Identifiants

pubmed: 32638786
doi: 10.1039/d0dt01007c
doi:

Substances chimiques

Antineoplastic Agents 0
Coordination Complexes 0
Macromolecular Substances 0
Polymers 0
Cobalt 3G0H8C9362
Copper 789U1901C5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9863-9881

Auteurs

Hiren Nath (H)

Department of Chemistry, Cotton University, Guwahati-781001, Assam, India. manjit.bhattacharyya@cottonuniversity.ac.in.

Debajit Dutta (D)

Department of Chemistry, Cotton University, Guwahati-781001, Assam, India. manjit.bhattacharyya@cottonuniversity.ac.in.

Pranay Sharma (P)

Department of Chemistry, Cotton University, Guwahati-781001, Assam, India. manjit.bhattacharyya@cottonuniversity.ac.in.

Antonio Frontera (A)

Departament de Química, Universitat de les Illes Balears, Crta de Valldemossa km 7.7, 07122 Palma de Mallorca, Baleares, Spain. toni.frontera@uib.es.

Akalesh K Verma (AK)

Department of Zoology, Cell & Biochemical Technology laboratory, Cotton University, Guwahati-781001, Assam, India. akhilesh@cottonuniversity.ac.in.

Miquel Barceló-Oliver (M)

Departament de Química, Universitat de les Illes Balears, Crta de Valldemossa km 7.7, 07122 Palma de Mallorca, Baleares, Spain. toni.frontera@uib.es.

Mary Devi (M)

Department of Zoology, Cell & Biochemical Technology laboratory, Cotton University, Guwahati-781001, Assam, India. akhilesh@cottonuniversity.ac.in.

Manjit K Bhattacharyya (MK)

Department of Chemistry, Cotton University, Guwahati-781001, Assam, India. manjit.bhattacharyya@cottonuniversity.ac.in.

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Classifications MeSH