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The first de novo designed inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2006 Jan 01; Vol. 16 (1), pp. 88-92. Date of Electronic Publication: 2005 Oct 19. - Publication Year :
- 2006
-
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.
- Subjects :
- Animals
Antimalarials pharmacology
Catalysis
Computer Simulation
Crystallography, X-Ray
Dihydroorotate Dehydrogenase
Enzyme Inhibitors chemistry
Humans
Inhibitory Concentration 50
Kinetics
Models, Chemical
Models, Molecular
Molecular Conformation
Protein Conformation
Software
Substrate Specificity
Ubiquinone chemistry
Antimalarials chemical synthesis
Chemistry, Pharmaceutical methods
Drug Design
Enzyme Inhibitors pharmacology
Oxidoreductases Acting on CH-CH Group Donors chemistry
Plasmodium falciparum enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 16
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 16236496
- Full Text :
- https://doi.org/10.1016/j.bmcl.2005.09.045