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1.
Top Curr Chem (Cham) ; 374(3): 28, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27573268

ABSTRACT

Calixarenes are considered as third generation supramolecules with hollow cavity-like architecture whereas nanoparticles are small entities with dimensions in the nanoscale. Many exciting achievements are seen when the calix system merges with nanoparticles which produces many fascinating facets in all fields of contemporary chemistry. The properties of nanoparticles which are tuned by calixarenes find applications in sensing, catalysis, molecular recognition, etc. Here, we have reviewed the chemistry of calix-based nanoparticles, and emphasis is laid on the modified, reducing, templated and stabilizing roles of calixarenes. This review covers the research being carried out in the domain of calix protected metal nanoparticles during last 18 years under the canopy of important 109 references. This article contains 58 figures which include 81 easy to understand structures. Calix-protected nanoparticles have enthralled researchers in the field of nanoscience with a tremendous growth in its applications, which heralds much promise to become in future a separate area of research.


Subject(s)
Calixarenes/chemistry , Nanoparticles/chemistry , Amino Acids/analysis , Gold/chemistry , Hydrocarbons/analysis , Metal Nanoparticles/chemistry , Pesticides/analysis , Pyrenes/chemistry , Silver/chemistry , Surface-Active Agents/chemistry
2.
Bioorg Med Chem Lett ; 26(3): 1005-1010, 2016 Feb 01.
Article in English | MEDLINE | ID: mdl-26725026

ABSTRACT

A series of novel substituted oxacalix[4]arene has been synthesized and explored for their biological profile by evaluating anticancer, antifungal and antibacterial properties. The derivatives have been characterized by various spectroscopic techniques such as IR, (1)H NMR, (13)C NMR and Mass spectrometry. Many compounds showed strong inhibition (MIC) in the range of ∼0-50 µM with interesting cytotoxic activities against Hela cells in particular. The compounds were theoretically evaluated by docking studies as potential histone deacetylase inhibitors (HDACi). The study indicates that compounds bound adequately with HDAC, and hence complemented the experimental findings.


Subject(s)
Antineoplastic Agents/chemical synthesis , Calixarenes/chemistry , Histone Deacetylase Inhibitors/chemical synthesis , Histone Deacetylases/chemistry , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Binding Sites , Calixarenes/chemical synthesis , Calixarenes/pharmacology , Cell Line, Tumor , Cell Survival/drug effects , Fungi/drug effects , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , HeLa Cells , Histone Deacetylase Inhibitors/chemistry , Histone Deacetylase Inhibitors/pharmacology , Histone Deacetylases/metabolism , Humans , Microbial Sensitivity Tests , Molecular Docking Simulation , Protein Structure, Tertiary
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