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The Structure−Activity Relationship of the Antimalarial Ozonide Arterolane (OZ277)
- Source :
- Journal of Medicinal Chemistry. 53:481-491
- Publication Year :
- 2009
- Publisher :
- American Chemical Society (ACS), 2009.
-
Abstract
- The structure and stereochemistry of the cyclohexane substituents of analogues of arterolane (OZ277) had little effect on potency against Plasmodium falciparum in vitro. Weak base functional groups were not required for high antimalarial potency, but they were essential for high antimalarial efficacy in P. berghei-infected mice. Five new ozonides with antimalarial efficacy and ADME profiles superior or equal to that of arterolane were identified.
- Subjects :
- Stereochemistry
Plasmodium falciparum
Molecular Conformation
Antimalarials
Heterocyclic Compounds, 1-Ring
Mice
Structure-Activity Relationship
chemistry.chemical_compound
Parasitic Sensitivity Tests
parasitic diseases
Drug Discovery
Animals
Structure–activity relationship
Ozonide
Potency
Spiro Compounds
Malaria, Falciparum
Arterolane
ADME
biology
Chemistry
Stereoisomerism
biology.organism_classification
Peroxides
Molecular Medicine
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 53
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....597e9be51453d7021377a69512c5262a
- Full Text :
- https://doi.org/10.1021/jm901473s