The art of building multifunctional metal-binding agents from basic molecular scaffolds for the potential application in neurodegenerative diseases

2012 ◽  
Vol 256 (19-20) ◽  
pp. 2308-2332 ◽  
Author(s):  
Cristina Rodríguez-Rodríguez ◽  
Maria Telpoukhovskaia ◽  
Chris Orvig
2015 ◽  
Vol 44 (19) ◽  
pp. 8760-8770 ◽  
Author(s):  
Marian E. Helsel ◽  
Katherine J. Franz

An exploration of synthetic metal-binding agents that alter the bioavailability of copper in ways that may provide therapeutic benefit against neurodegenerative diseases, cancer, infection, and other diseases where misappropriated metal ions are suspected of exacerbating cellular damage.


Geriatrics ◽  
2016 ◽  
Vol 1 (4) ◽  
pp. 29 ◽  
Author(s):  
Jintang Wang ◽  
Yuetao Song ◽  
Maolong Gao ◽  
Xujing Bai ◽  
Zheng Chen

1970 ◽  
Vol 27 (1) ◽  
pp. 59-69 ◽  
Author(s):  
Douglas A. Wolfe

Nearly all the zinc in oysters is bound, either to soluble high-molecular weight proteins or to structural cellular components such as cell membranes. Oyster alkaline phosphatase is a zinc metalloenzyme, as indicated by in vitro inhibition studies with various metal-binding agents. Dialysis of soluble tissue extracts at pH 7–9 removes up to 96% of the total zinc without effect on alkaline phosphatase. If alkaline phosphatase is considered representative of the metabolic functions of zinc in oysters, most of the zinc accumulated by oysters must be superfluous to the animal's requirements.


2005 ◽  
Vol 64 (1) ◽  
pp. 120-123 ◽  
Author(s):  
M. Pallàs ◽  
E. Verdaguer ◽  
E.G. Jordà ◽  
A. Jiménez ◽  
A.M. Canudas ◽  
...  

1991 ◽  
Vol 43 (2-3) ◽  
pp. 148
Author(s):  
Vincent L. Pecoraro ◽  
Myoung Soo Lah ◽  
Dimitris P. Kessissoglou ◽  
Jeff Kampf ◽  
Brian Gibney

2010 ◽  
Vol 25 (1) ◽  
pp. 21-30 ◽  
Author(s):  
Cristina Rodríguez-Rodríguez ◽  
Albert Rimola ◽  
Jorge Alí-Torres ◽  
Mariona Sodupe ◽  
Pilar González-Duarte

2020 ◽  
Vol 18 ◽  
Author(s):  
Graziella dos Reis Franco ◽  
Scott Smid ◽  
Cláudio Viegas

: In the last few years research into Cannabis and its constituent phytocannabinoids has burgeoned, particularly in the potential application of novel cannabis phytochemicals for the treatment of diverse illnesses related to neurodegeneration and dementia, including Alzheimer's (AD), Parkinson's (PD) and Huntington's disease (HD). To date, these neurological diseases have mostly relied on symptomatological management. However, with an aging population globally, the search for more efficient and disease-modifying treatments that could delay or mitigate disease progression is imperative. In this context, this review aims to present a state of art in the research with cannabinoids and novel cannabinoid-based drug candidates that have been emerged as novel promising alternatives for drug development and innovation in the therapeutics of a number of diseases, especially those related to CNS-disturbance and impairment.


2018 ◽  
Vol 16 (2) ◽  
pp. 71-79 ◽  
Author(s):  
Federico Brucoli

Tuberculosis, an ancient infectious disease caused by Mycobacterium tuberculosis, ranks as one of the top ten killers worldwide. The limited number of validated targets and scarce therapeutic options demand that renewed efforts should be made to identify tuberculosis drugs with novel mechanisms of action. To this end, mycobacterial DNA might represent a potential target for the development of effective anti-tubercular compounds. In particular, the minor groove of DNA offers an important recognition site for small-molecules that can be programmed to bind to this region in a sequence-selective manner to disrupt mycobacterial transcription factors activity and ultimately cause bacterial cell death. This review describes the structural features of the DNA-minor groove, the requirements for small molecules to bind to this site and the remarkable biophysical and antibacterial properties of DNA-minor groove binding agents, including netropsin, distamycin and their poly-heterocyclic analogues, diamidines, benzimidazole-containing molecules, duocarmycins and pyrrolo[2,1-c][1,4]benzodiazepines (PBDs). Furthermore, the ability of selected heterocyclic-polyamides and PBDs to significantly inhibit the growth of pathogenic, slow-growing M. tuberculosis and other non-pathogenic mycobacterial strains is highlighted. In summary, DNA-minor groove binding agents may serve as molecular scaffolds for the design of highly efficient probes to treat M. tuberculosis infections.


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