Yusuf Hamied Department of Chemistry

Professor David Spring

Professor of Chemistry & Chemical Biology

 

Our research interests originate from a desire to understand and exploit biological systems using organic synthesis primarily. Listed below are areas of research that we are exploring; for more detailed information visit the Spring Group web pages.

We collaborate with many chemical companies and academic groups around the world. The scientific education of group members in organic synthesis is given a high priority; however, they are encouraged also to learn and perform new techniques relating to their projects with our industrial and academic collaborators. Every effort is made so that group members achieve their career ambitions, usually jobs in academia or the chemical industries.

Spring Group Figure

 

 

Watch Professor David Spring discuss his research

Take a quick tour of the Spring Lab

For more detailed information please visit the Spring Group research pages.

Teaching

If you are looking for the teaching material from my lecture courses, then please go to the Moodle website.

Publications

For a list of all our publications please visit the Spring Group publication page.

Publications

Photoswitchable PROTACs: Visible light activated degradation of the androgen receptor
E Fowler, A Hock, D O'Donovan, J Gorman, G Fumagalli, R Friend, D Spring
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2019)
258
Cycloaddition Strategies for the Synthesis of Diverse Heterocyclic Spirocycles for Fragment-Based Drug Discovery
TA King, HL Stewart, KT Mortensen, AJP North, HF Sore, DR Spring
European Journal of Organic Chemistry
(2019)
2019
(doi: 10.1002/ejoc.201900847)
Hotspots API: A toolkit for the application of Fragment Hotspot Mapping to Structure Based Drug Discovery
P Curran, C Radoux, M Smilova, A Higueruelo, R Sykes, A Bradley, W Pitt, D Spring, T Blundell, J Cole
Acta Crystallographica Section A: Foundations and advances
(2019)
75
(doi: 10.1107/s0108767319097782)
Macrocyclisation and functionalisation of unprotected peptides via divinyltriazine cysteine stapling.
NS Robertson, SJ Walsh, E Fowler, M Yoshida, SM Rowe, Y Wu, HF Sore, JS Parker, DR Spring
Chem Commun (Camb)
(2019)
55
(doi: 10.1039/c9cc05042f)
Targeted covalent inhibitors of MDM2 using electrophile-bearing stapled peptides
J Charoenpattarapreeda, YS Tan, J Iegre, SJ Walsh, E Fowler, RS Eapen, Y Wu, HF Sore, CS Verma, L Itzhaki, DR Spring
Chemical Communications
(2019)
55
(doi: 10.1039/c9cc04022f)
Strategies for the Diversity-Oriented Synthesis of Macrocycles
KT Mortensen, TJ Osberger, TA King, HF Sore, DR Spring
Chemical Reviews
(2019)
119
(doi: 10.1021/acs.chemrev.9b00084)
Cleavable linkers in antibody-drug conjugates.
JD Bargh, A Isidro-Llobet, JS Parker, DR Spring
Chemical Society reviews
(2019)
48
(doi: 10.1039/c8cs00676h)
Spirocycles as Rigidified sp3-Rich Scaffolds for a Fragment Collection.
A Sveiczer, AJP North, N Mateu, SL Kidd, HF Sore, DR Spring
Organic Letters
(2019)
21
(doi: 10.1021/acs.orglett.9b01499)
Efficient development of stable and highly functionalised peptides targeting the CK2α/CK2β protein-protein interaction.
J Iegre, P Brear, DJ Baker, YS Tan, EL Atkinson, HF Sore, DH O' Donovan, CS Verma, M Hyvönen, DR Spring
Chemical science
(2019)
10
(doi: 10.1039/c9sc00798a)
Development of novel CK2 inhibitors: From small molecules to conformationally constrained peptides targeting allosteric binding sites
J Iegre, P Brear, D Spring
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2019)
257

Research Group

Research Interest Groups

Telephone number

01223 336498

Email address

spring@ch.cam.ac.uk

College

Trinity College
Yusuf Hamied Department of Chemistry
Lensfield Road
Cambridge
CB2 1EW
T: +44 (0) 1223 336300
enquiries@ch.cam.ac.uk
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