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Design, Synthesis and Biological Evaluation of Innovative Broad-Spectrum Reactivators of neurotoxic organophosphorus inhibited human CholinEsterase

ABG-137218 Thesis topic
2026-03-26 Public funding alone (i.e. government, region, European, international organization research grant)
Ecole Européenne de Chimie, Polymères et Matériaux de Strasbourg (ECPM))
- Grand Est - France
Design, Synthesis and Biological Evaluation of Innovative Broad-Spectrum Reactivators of neurotoxic organophosphorus inhibited human CholinEsterase
  • Chemistry
  • Biochemistry
reactivators of Cholinesterases, antidotes, nerve agents and pesticides, BBB penetration, central antidotes

Topic description

Background

Organophosphorus nerve agents (OPNA) have experienced a resurgence recently with their large-scale use against civilians during the attacks in Syria (2013, 2017), the assassination of Kim Jong-nam in Malaysia (2017), the poisoning of Sergei and Yulia Skripal in the UK (2018) and Alexeï Navalny in Russia (2020), strongly renewing the importance of antidotes development against these lethal synthetic compounds.1 Organophosphorus pesticides (OPP) used for agricultural purposes are also regarded as a potential threat in a terrorist context. According to the World Health Organization (WHO), 3 million cases of OPP poisoning occur in the world, causing 200,000 deaths per year in developing countries. Due to their ease of production, organophosphorus compounds (OP) have been developed and stock-piled on a large scale, increasing the population's chemical risk. Recently, the emergence of Novichok as the fourth generation OPNA and its use against civilians (2018, 2020) have re-emphasized the need for broad-spectrum medical countermeasures (MCM) against these agents to ensure the global safety of all civilians in the world, preventing nerve agent intoxications.

The high toxicity of OPNA is caused by covalent binding to a serine hydroxyl residue at the active site of the pivotal acetylcholinesterase, key enzyme of the cholinergic neurotransmission system.

Subsequent accumulation of the acetylcholine (ACh) neurotransmitter and overstimulation of muscarinic and nicotinic receptors results in the development of multiple characteristic clinical symptoms, such as miosis, muscle spasm, convulsion, paralysis, breathing failure, and finally death due to respiratory arrest.

Recently, our research group discovered and patented the first (i) broad spectrum hybrid reactivators, and the first fluoro-hybrid reactivators of inhibited cholinesterases, opening a new era in this domain of investigation. Expanding the scope of this new family of original molecules is crucial for the development of the new generation antidotes.

 

The aims of this Thesis Research Project are to design, synthesize and evaluate biologically novel multifunctional AChE reactivators on mice and zebra fish model, with high blood brain barrier (BBB) in vivo penetration ability, low hepatotoxicity and with broad reactivation spectrum capabilities. The work will be realized at ICPEES and between collaborating groups, including Institut de Recherche Biomédicale des Armées (IRBA), the Institute de Biologie Structurale of Grenoble (CEA). Candidates should expect to experience exciting scientific adventures within an interdisciplinary worldwide research environment, at the crossroads of organic and bio-organic chemistry, biology and structural biology.

 

Link to the doctoral school of the university of strasbourg competition:

https://amethis3.unistra.fr/amethis-client/prd/consulter?etat=ouvert

 

Starting date

2026-10-01

Funding category

Public funding alone (i.e. government, region, European, international organization research grant)

Funding further details

Competition organised by the University of Strasbourg’s Doctoral School

Presentation of host institution and host laboratory

Ecole Européenne de Chimie, Polymères et Matériaux de Strasbourg (ECPM))

ICPEES (Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé, UMR 7515 CNRS and Université de Strasbourg) was created in January 2013 when two laboratories, the "Laboratoire des matériaux, surfaces et procédés pour la catalyse" (LMSPC) and the "Laboratoire d'ingénierie des polymères pour les hautes technologies" (LIPHT), decided to merge. At the time of the merger, the three LIPHT teams and the seven LMSPC teams were structured into three research departments: Catalysis and Materials, Molecular and Analytical Chemistry, and Polymer Engineering.

The Institute's cross-disciplinary skills enable it to address global issues ranging from molecule synthesis to the development of final objects for applications in the energy, environment and health sectors. The strong involvement of the unit's teams in fundamental research with a view to applications has enabled the laboratory to position itself across the entire value chain and to acquire an international reputation. Academic collaborations, both national and international, have also contributed to the development of new, currently unexploited lines of research. The downstream developments of the unit's research have also enabled us to forge numerous collaborations with the socio-economic world, providing concrete solutions to various societal demands and developing new processes.

The Institute has a total workforce of around 130, including some 60 permanent staff and 70 non-permanent staff (PhD students, post-docs and technical staff). The unit also hosts a number of researchers seconded from industrial partners as part of joint research structures (LabCom) and industrial collaborations.

PhD title

Doctorat en Chimie de l'Université de Strasbourg

Country where you obtained your PhD

France

Institution awarding doctoral degree

UNIVERSITE DE STRASBOURG

Graduate school

Sciences chimiques

Candidate's profile

HOW TO APPLY: The candidate should have a MASTER in synthetic Organic Chemistry or in Chemistry and Biology with a strong background in organic synthesis. Strong motivation for research in a competitive area is expected. Applications (CV +motivation letter as well as 3 references) should be sent by e-mail to: rachid.baati@unistra.fr

2026-04-30
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