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Overcoming chloroquine resistance in malaria: Design, synthesis and structure-activity relationships of novel chemoreversal agents
- Publication Year :
- 2016
- Publisher :
- Elsevier, 2016.
-
Abstract
- Malaria remains a significant infectious disease with even artemisinin-based therapies now facing resistance in the field. Development of new therapies is urgently needed, either by finding new compounds with unique modes of action, or by reversing resistance towards known drugs with 'chemosensitizers' or 'chemoreversal' agents (CRA). Concerning the latter, we have focused on the resistance mechanisms developed against chloroquine (CQ). We have synthesized a series of compounds related to previously identified CRAs, and found promising novel compounds. These compounds show encouraging results in a coumarin labeled chloroquine uptake assay, exhibiting a dose response in resensitising parasites to the antimalarial effects of chloroquine. Selected compounds show consistent potency across a panel of chloroquine and artemisinin sensitive and resistant parasites, and a wide therapeutic window. This data supports further study of CRAs in the treatment of malaria and, ultimately, their use in chloroquine-based combination therapies.
- Subjects :
- 0301 basic medicine
Models, Molecular
Plasmodium falciparum
Drug Resistance
Molecular Conformation
Drug resistance
Chemistry Techniques, Synthetic
Pharmacology
01 natural sciences
Cell Line
03 medical and health sciences
Antimalarials
Inhibitory Concentration 50
Mice
Structure-Activity Relationship
Chloroquine
Drug Discovery
medicine
Structure–activity relationship
Animals
Artemisinin
Chloroquine resistance
biology
Dose-Response Relationship, Drug
Chemistry
Organic Chemistry
Biological Transport
General Medicine
medicine.disease
biology.organism_classification
0104 chemical sciences
010404 medicinal & biomolecular chemistry
030104 developmental biology
Infectious disease (medical specialty)
Drug Design
Malaria
medicine.drug
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....560922cb65a007f384fc9dc76213f7bc