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PhD in Synthetic Medicinal Chemistry Targeting Blood Coagulation Factors XIa and XIIa

University of Galway School of Biological and Chemical Sciences
✓ Fully Funded ⏰ Closing Soon 🎓 Chemistry synthetic chemistry medicinal chemistry drug discovery cardiovascular diseases antithrombotic agents blood coagulation enzyme inhibition small molecule synthesis

Explore the development of novel inhibitors targeting coagulation factors XIa and XIIa to create safer cardiovascular therapies. Combine advanced synthetic chemistry and biochemical evaluation in a cutting-edge research environment at University of Galway.

AI-generated overview

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Why This Research Matters

Cardiovascular diseases such as thrombosis present major global health challenges due to high mortality and complications from existing treatments. This research aims to develop safer, more selective antithrombotic drugs, lowering bleeding risks and improving treatment options, potentially transforming cardiovascular healthcare outcomes.

Medicinal Chemistry Organic Chemistry Pharmacy Natural Products

Project Description

Project Overview

This project focuses on discovering novel small-molecule inhibitors targeting intrinsic blood coagulation cascade components, specifically factors XIa and XIIa. Thrombosis is a leading cause of mortality via myocardial infarction and ischemic stroke, and current antithrombotic drugs pose bleeding risks. The aim is to create safer, selective antithrombotic agents through advanced synthetic and medicinal chemistry.

What You Will Do

The candidate will join the School of Biological and Chemical Sciences at the University of Galway, supervised by Dr. Dmitrii Kalinin. The research involves multistep organic synthesis combined with microscale parallel synthesis to generate diverse small molecule libraries. These will be evaluated with enzyme inhibition assays and blood coagulation functional tests, providing experience bridging synthetic chemistry, medicinal chemistry, and pharmacology.

Expected Outcomes

The research is expected to yield new therapeutic candidates with high selectivity and improved safety profiles for treatment of cardiovascular diseases. The project also offers valuable interdisciplinary skills in drug discovery applicable to both academic and industrial sectors.

Why This Matters

Thrombosis-related diseases cause significant global mortality. Developing safer antithrombotic agents can reduce bleeding complications associated with current therapies, improving patient outcomes and addressing urgent medical needs worldwide.

Entry Requirements

A first or upper second class honours degree or a master’s in chemistry, medicinal chemistry, pharmacy, or related field. Experience in organic small molecule synthesis, proficiency in NMR structure elucidation, familiarity with IR and HPLC analytical techniques, and interest in chemistry-biology interdisciplinary research. International applicants should have a minimum IELTS score of 6.5.

How to Apply

Submit a one-page motivation letter and a CV including education and research experience, plus contact details of two referees, directed to Dr. Dmitrii Kalinin. Application deadline: 2026-05-05 at 17:00 Irish time. Further details at https://www.linkedin.com/posts/dmitrii-v-kalinin_phd-scholarship-activity-7448340043615645696-PmUJ

Eligibility

UK/Home
EU
International

Supervisor Profile

DD
Dr. Dmitrii Kalinin
University of Galway, School of Biological and Chemical Sciences

Dr. Dmitrii Kalinin specializes in synthetic and medicinal chemistry with a focus on drug discovery, especially creating and evaluating small molecule therapeutic candidates. His research integrates organic synthesis with pharmacological analysis to address cardiovascular and other significant diseases. He is recognized for combining traditional and cutting-edge synthesis techniques to develop novel bioactive compounds.

Key Publications

2018 134 citations
Characterization of histone deacetylase 8 (HDAC8) selective inhibition reveals specific active site structural and functional determinants
2017 89 citations
LpxC inhibitors: a patent review (2010-2016)
2021 50 citations
Factor XII (a) inhibitors: a review of the patent literature
2016 50 citations
Insights into the zinc-dependent deacetylase LpxC: biochemical properties and inhibitor design
2018 48 citations
Development of novel quinoxaline-based κ-opioid receptor agonists for the treatment of neuroinflammation

Research Contributions

Development and characterization of selective histone deacetylase 8 (HDAC8) inhibitors with specific structural and functional determinants.
Provides insights for targeted drug design and therapeutic strategies involving HDAC8.
Review and analysis of LpxC inhibitors, including biochemical properties and inhibitor design.
Supports the development of antibacterial agents targeting zinc-dependent enzymes.
Research on Factor XII(a) inhibitors focusing on patent literature and novel anticoagulant properties.
Advances anticoagulant therapy by identifying potential inhibitors of blood coagulation factors.
Design and synthesis of quinoxaline-based κ-opioid receptor agonists to address neuroinflammation.
Offers new therapeutic options for neuroinflammatory diseases through opioid receptor modulation.

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