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Crassiflorone derivatives that inhibit Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase (TbGAPDH) and Trypanosoma cruzi trypanothione reductase (TcTR) and display trypanocidal activity
- Publication Year :
- 2017
-
Abstract
- none 20 si Crassiflorone is a natural product with anti-mycobacterial and anti-gonorrhoeal properties, isolated from the stem bark of the African ebony tree Diospyros crassiflora. We noticed that its pentacyclic core possesses structural resemblance to the quinone-coumarin hybrid 3, which we reported to exhibit a dual-targeted inhibitory profile towards Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase (TbGAPDH) and Trypanosoma cruzi trypanothione reductase (TcTR). Following this basic idea, we synthesized a small library of crassiflorone derivatives 15-23 and investigated their potential as anti-trypanosomatid agents. 19 is the only compound of the series showing a balanced dual profile at 10 μM (% inhibitionTbGAPDH= 64% and % inhibitionTcTR= 65%). In phenotypic assay, the most active compounds were 18 and 21, which at 5 μM inhibited Tb bloodstream-form growth by 29% and 38%, respectively. Notably, all the newly synthesized compounds at 10 μM did not affect viability and the status of mitochondria in human A549 and 786-O cell lines, respectively. However, further optimization that addresses metabolic liabilities including solubility, as well as cytochromes P450 (CYP1A2, CYP2C9, CYP2C19, and CYP2D6) inhibition, is required before this class of natural product-derived compounds can be further progressed. Uliassi, Elisa; Fiorani, Giulia; Krauth-Siegel, R. Luise; Bergamini, Christian; Fato, Romana; Bianchini, Giulia; Carlos Menéndez, J.; Molina, Maria Teresa; López-Montero, Eulogio; Falchi, Federico; Cavalli, Andrea; Gul, Sheraz; Kuzikov, Maria; Ellinger, Bernhard; Witt, Gesa; Moraes, Carolina B.; Freitas-Junior, Lucio H.; Borsari, Chiara; Costi, Maria Paola; Bolognesi, Maria Laura* Uliassi, Elisa; Fiorani, Giulia; Krauth-Siegel, R. Luise; Bergamini, Christian; Fato, Romana; Bianchini, Giulia; Carlos Menéndez, J.; Molina, Maria Teresa; López-Montero, Eulogio; Falchi, Federico; Cavalli, Andrea; Gul, Sheraz; Kuzikov, Maria; Ellinger, Bernhard; Witt, Gesa; Moraes, Carolina B.; Freitas-Junior, Lucio H.; Borsari, Chiara; Costi, Maria Paola; Bolognesi, Maria Laura*
- Subjects :
- 0301 basic medicine
Parasitic Sensitivity Test
Models, Molecular
Crassiflorone
Trypanosomiasi
Dehydrogenase
01 natural sciences
NADPH Oxidoreductases
chemistry.chemical_compound
Parasitic Sensitivity Tests
Coumarins
Models
Drug Discovery
NADH, NADPH Oxidoreductases
Leishmaniasis
Glyceraldehyde 3-phosphate dehydrogenase
Natural products
Tumor
biology
Trypanocidal Agent
Molecular Structure
Quinones
Glyceraldehyde-3-Phosphate Dehydrogenases
General Medicine
Trypanocidal Agents
Biochemistry
Quinone
Glyceraldehyde-3-phosphate dehydrogenase
Diospyros crassiflora
Drug
Human
Leishmaniasi
Trypanosoma cruzi
Trypanosoma brucei brucei
Trypanosoma brucei
Coumarin
Natural product
Cell Line
Dose-Response Relationship
03 medical and health sciences
Structure-Activity Relationship
Trypanosomiasis
Cell Line, Tumor
Structure–activity relationship
Humans
Trypanocidal agent
Trypanocidal activity
Pharmacology
Dose-Response Relationship, Drug
010405 organic chemistry
Drug Discovery3003 Pharmaceutical Science
Organic Chemistry
Molecular
biology.organism_classification
0104 chemical sciences
030104 developmental biology
Trypanothione reductase
chemistry
NADH
biology.protein
NADH, NADPH Oxidoreductase
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....bd27927f3e2d6ad95ba8f890079d66db