Details of Grant 

EPSRC Reference:	EP/N00969X/1
Title:	Cyanamides: Exploring New Approaches Towards Heterocyclic Scaffolds
Principal Investigator:	Sharma, Dr P
Other Investigators:
Researcher Co-Investigators:
Project Partners:
Department:	School of Chemistry
Organisation:	University of Lincoln
Scheme:	First Grant - Revised 2009
Starts:	01 March 2016	Ends:	28 February 2017	Value (£):	98,743
EPSRC Research Topic Classifications:	Chemical Synthetic Methodology
EPSRC Industrial Sector Classifications:	Pharmaceuticals and Biotechnology
Related Grants:
Panel History:	Panel Date Panel Name Outcome 23 Sep 2015 EPSRC Physical Sciences Chemistry - September 2015 Announced
Summary on Grant Application Form
The development of new medicines are essential to ensure improvement in the health of the world's population, and to tackle unmet medical needs. Furthermore, with the advances in genomic research, it is estimated that several thousand new biological targets associated with medical conditions will soon be identified. This exerts enormous pressure on scientists to design, develop and deliver new molecules in a timely fashion to meet these demands. Traditionally, the search for new lead molecules in drug discovery has been mainly focused on natural sources or screening existing compound libraries available from the pharmaceutical banks. Unfortunately, these processes could be time consuming as well as hitting dead ends with the relatively limited structural diversity and complexity of molecular scaffolds available. This project will deliver new chemical methods for the construction of novel molecular cores from a simple, readily available and low cost starting material. Heterocyles are carbon based ring compounds containing at least one heteroatom (such as oxygen, nitrogen, sulphur) in the ring and, are frequently the essential active component of drugs. The key innovation of this proposal is the invention, development and application of a new set of chemical reagents, called cyanamides. These reagents contain unique chemical linkages with multiple functionality, and are important in performing multiple roles in chemical synthesis. The new chemistry described utilises very mild conditions to deliver arrays of structurally complex and diverse molecules. The process will lead to the identification of new chemical pathways for the construction of heterocyclic systems, which are key to the drug discovery programme. Furthermore as the protocol involves coupling of two fragments, there is significant scope to explore a wide variety of functional groups that could be introduced directly onto the heterocyclic core of the molecule. This will enable rapid access to diverse molecular frameworks that are not currently represented. This will lead to the generation of potential lead compounds against a wide variety of biological targets. Collaborative research both within University and Industry will help evaluate the new compounds as potential drugs. The wider outcome of the proposed project will have a positive contribution to science and society in general.
Key Findings
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
Potential use in non-academic contexts
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
Impacts
Description This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk Summary Date Materialised
Sectors submitted by the Researcher
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
Project URL:
Further Information:
Organisation Website:	http://www.lincoln.ac.uk