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dc.contributor.author
Le Douaron, Gael  
dc.contributor.author
Ferrié, Laurent  
dc.contributor.author
Sepulveda Diaz, Julia E.  
dc.contributor.author
Seon Méniel, Blandine  
dc.contributor.author
Acuña, Leonardo  
dc.contributor.author
Raisman Vozari, Rita  
dc.contributor.author
Michel, Patrick P.  
dc.contributor.author
Figadere, Bruno  
dc.date.available
2018-02-27T15:23:32Z  
dc.date.issued
2017-09  
dc.identifier.citation
Le Douaron, Gael; Ferrié, Laurent ; Sepulveda Diaz, Julia E.; Seon Méniel, Blandine ; Acuña, Leonardo; et al.; Correction to: Identification of a novel 1,4,8-triazaphenanthrene derivative as a neuroprotectant for dopamine neurons vulnerable in Parkinson's disease; American Chemical Society; ACS Chemical Neuroscience; 8; 10; 9-2017; 2347-2347  
dc.identifier.issn
1948-7193  
dc.identifier.uri
http://hdl.handle.net/11336/37253  
dc.description.abstract
Parkinson's disease (PD) is a chronic degenerative disorder characterized by typical motor symptoms caused by the death of dopamine (DA) neurons in the midbrain and ensuing shortage of DA in the striatum, at the level of nerve terminals. No curative treatment is presently available for PD in clinical practice. In our search for neuroprotectants in PD, we generated new 1,4,8-triazaphenanthrenes by combining 6-endo-dig-cycloisomerization of propargylquinoxalines and Suzuki or Sonogashira cross-coupling reactions. Neuroprotection assessment of newly synthesized 1,4,8-triazaphenanthrenes in a PD cellular model resulted in the discovery of a new hit compound PPQ (5m). Neuroprotection by 5m was concentration-dependent and the result of a combined effect on intracellular calcium release channels and astroglial cells. Of interest, 5m also counteracted DA cell loss in a mouse model of PD, making this molecule a promising candidate for PD treatment.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Medicinal Chemistry  
dc.subject
Neurodegenerative Diseases  
dc.subject
Phenotypic Screening  
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Primary Neuronal Cultures  
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Suzuki Coupling Reaction  
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Otras Ciencias Biológicas  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
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Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.subject.classification
Inmunología  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Correction to: Identification of a novel 1,4,8-triazaphenanthrene derivative as a neuroprotectant for dopamine neurons vulnerable in Parkinson's disease  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-11-03T19:10:11Z  
dc.journal.volume
8  
dc.journal.number
10  
dc.journal.pagination
2347-2347  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Le Douaron, Gael. Universite Paris Sud; Francia. Universite Pierre et Marie Curie; Francia  
dc.description.fil
Fil: Ferrié, Laurent. Universite Paris Sud; Francia  
dc.description.fil
Fil: Sepulveda Diaz, Julia E.. Universite Pierre et Marie Curie; Francia  
dc.description.fil
Fil: Seon Méniel, Blandine. Universite Paris Sud; Francia  
dc.description.fil
Fil: Acuña, Leonardo. Universite Pierre et Marie Curie; Francia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Raisman Vozari, Rita. Universite Pierre et Marie Curie; Francia  
dc.description.fil
Fil: Michel, Patrick P.. Universite Pierre et Marie Curie; Francia  
dc.description.fil
Fil: Figadere, Bruno. Universite Paris Sud; Francia  
dc.journal.title
ACS Chemical Neuroscience  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acschemneuro.7b00352  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acschemneuro.7b00352