Opendata, web and dolomites

TS4NC SIGNED

TS4NC: Therapeutic S4N Chelation targeting Alzheimer's Disease.

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 TS4NC project word cloud

Explore the words cloud of the TS4NC project. It provides you a very rough idea of what is the project "TS4NC" about.

drug    consideration    planar    activation    redox    carriers    stress    normal    treatment    industry    discovering    carry    cu    affinity    square    atcun    horizons    act    circulation    prevailing    synergistic    inflammatory    restoration    brain    boost    professional    simply    clinical    arrest    scientific    lies    maturity    chelating    last    back    peptide    metals    ad    hypotheses    strategy    shed    equally    failed    pharmaceutical    despite    redistributing    mimics    greatest    reduce    organism    4n    put    class    candidate    perform    efforts    assisting    neuronal    mpacs    anti    attenuating    s4ns    active    enormous    releasing    trials    cascade    contrary    ions    oxidative    novelty    inhibit    beta    aggregates    amyloid    regulation    herein    decade    linked    neuroglia    disease    neurons    helping    metal    biometal    forms    physiological    copper    complexes    motif    alzheimer    neuroprotection    peptides    compounds    career    discovery    academia    agents    conclude    terminus    significantly    s4n    eliminating    selectivity    light    aggregation    delivering    sequester    cells    natural    ts4nc    mcsa    nonregulated    multifunctional    homeostasis    protein    cycles    fellowship   

Project "TS4NC" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-09-01   to  2022-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 212˙933.00

Map

 Project objective

Despite enormous research efforts across academia and pharmaceutical industry, all clinical trials over the last decade have failed in finding a treatment for Alzheimer’s Disease (AD) which remains one of the greatest challenges in drug discovery. Taking consideration all together three prevailing AD hypotheses: Amyloid Cascade, Metal Ions and Oxidative Stress, researchers conclude that loss of neurons is due to a high level of oxidative stress produced by nonregulated redox active metal ions such as copper linked to different forms/aggregates of amyloid-β (Aβ) peptides. Therefore, the regulation of metal homeostasis is a key target for drug development. Herein, we propose a new class of multifunctional agents – S4Ns, which not only sequester Cu ions from their Aβ complexes and arrest their redox cycles, thus reduce oxidative stress in the neuronal cells, inhibit Aβ aggregation, inhibit neuroglia activation and provide anti-inflammatory effects, delivering overall neuroprotection, but also put Cu back into normal physiological circulation by releasing Cu to natural Cu-carriers. The key novelty of this approach lies in that S4N mimics the N-terminus of Aβ4-x peptide (ATCUN motif), providing 4N square planar Cu(II) coordination with high affinity and selectivity. In general, S4Ns do not act as traditional chelating agents by simply eliminating metals from the organism, on the contrary they perform as Metal–Protein Attenuating Compounds (MPACs) by redistributing and assisting in the restoration of brain biometal homeostasis. This synergistic but novel strategy will allow us to carry out a comprehensive study of the new compounds and shed light into discovering promising drug candidate. Of equally importance, TS4NC MCSA will open new research horizons and significantly boost scientific career of the applicant, by helping her to reach professional maturity during the fellowship.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "TS4NC" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "TS4NC" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

DEF2DEV (2019)

Identification of the mode of action of plant defensins during root development and plant defense responses.

Read More  

CREDit (2020)

Chronological REference Datasets and Sites (CREDit) towards improved accuracy and precision in luminescence-based chronologies

Read More  

TRANSMODERN (2019)

Untranslatable Modernity: Modern Literary Theory from Europe to Iran

Read More