Heikkila, T., Thirumalairajan, S., Davies, M. et al. (4 more authors) (2006) The first de novo designed inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase. Bioorganic and Medicinal Chemistry Letters, 16 (1). pp. 88-92. ISSN: 0960-894X
Abstract
The de novo molecular design program SPROUT has been applied to the X-ray crystal structures of Plasmodium and human dihydroorotate dehydrogenase, respectively. The resulting design templates were used to prepare a series of molecules which, in keeping with predictions, showed useful levels of species-selective enzyme inhibition.
Metadata
| Item Type: | Article |
|---|---|
| Authors/Creators: |
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| Keywords: | Medicinal chemistry; Oxoreductases; Inhibitors; Molecular recognition; Molecular modelling |
| Dates: |
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| Institution: | The University of Leeds |
| Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Biology (Leeds) |
| Date Deposited: | 27 Apr 2026 11:41 |
| Last Modified: | 27 Apr 2026 11:41 |
| Status: | Published |
| Publisher: | Elsevier |
| Identification Number: | 10.1016/j.bmcl.2005.09.045 |
| Sustainable Development Goals: | |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:233398 |
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