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dc.contributor.author
Solis, Carlos Marcelo
dc.contributor.author
Salazar, Mario Oscar
dc.contributor.author
Ramallo, Ivana Ayelen
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García, Paula
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Furlan, Ricardo Luis Eugenio
dc.date.available
2021-04-20T12:05:56Z
dc.date.issued
2019-09
dc.identifier.citation
Solis, Carlos Marcelo; Salazar, Mario Oscar; Ramallo, Ivana Ayelen; García, Paula; Furlan, Ricardo Luis Eugenio; A Tyrosinase Inhibitor from a Nitrogen-Enriched Chemically Engineered Extract; American Chemical Society; ACS Combinatorial Science; 21; 9; 9-2019; 622-627
dc.identifier.issn
2156-8952
dc.identifier.uri
http://hdl.handle.net/11336/130440
dc.description.abstract
The enzyme tyrosinase is involved in the biosynthesis of melanin and the enzymatic browning of fruits and vegetables, and therefore, its inhibitors have potential to treat hyperpigmentary disorders or to function as food antibrowning agents. The use of hydrazine monohydrate as a reagent to prepare chemically engineered extracts can lead to semisynthetic compounds that contain the portion N-N, a fragment rarely found in natural products and present in some tyrosinase inhibitors. Here, we report the tyrosinase inhibition screening of a series of chemically engineered extracts that are diversified by reaction with hydrazine. LC-MS was used to evaluate the change in composition produced by the reaction. Bioguided fractionation of the most active chemically engineered extract, prepared from Matricaria recutita L., led to the discovery of a pyrazole that inhibits tyrosinase with an IC50 value of 28.20 ± 1.13 μM. This compound was produced by a one-pot double chemical transformation of its natural precursor, which includes an unexpected selective removal of one-OH group.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
CHEMICALLY ENGINEERED EXTRACTS
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CHEMO-DIVERSIFICATION
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DEHYDROXYLATION
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FLAVONE
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HYDRAZINE
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PYRAZOLE
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TYROSINASE INHIBITOR
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Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
A Tyrosinase Inhibitor from a Nitrogen-Enriched Chemically Engineered Extract
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-11-25T17:48:50Z
dc.identifier.eissn
2156-8944
dc.journal.volume
21
dc.journal.number
9
dc.journal.pagination
622-627
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Washington D. C.
dc.description.fil
Fil: Solis, Carlos Marcelo. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas.; Argentina
dc.description.fil
Fil: Salazar, Mario Oscar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas.; Argentina
dc.description.fil
Fil: Ramallo, Ivana Ayelen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas.; Argentina
dc.description.fil
Fil: García, Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas.; Argentina
dc.description.fil
Fil: Furlan, Ricardo Luis Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas.; Argentina
dc.journal.title
ACS Combinatorial Science
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acscombsci.9b00064
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acscombsci.9b00064
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