Denisse de Loera

Dr. Denisse de Loera

Universidad Autónoma de San Luis Potosí, San Luis Potosí, Mexico
orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 March 2023 in Pharmaceuticals
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Journal Article
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GNGabriela Navarro-Tovar
Gabriela Navarro-Tovar
SVSarai Vega-Rodríguez
Sarai Vega-Rodríguez
ELElisa Leyva
Elisa Leyva
SLSilvia Elena Loredo-Carrillo
Silvia Elena Loredo-Carrillo
Denisse de LoeraDenisse de Loera
Denisse de Loera
LLLluvia I. López
Lluvia I. López
Natural product derivatives are essential in searching for compounds with important chemical, biological, and medical applications. Naphthoquinones are secondary metabolites found in plants and are used in traditional medicine to treat diverse human diseases. Considering this, the synthesis of naphthoquinone derivatives has been explored to contain compounds with potential biological activity. It has been reported that the chemical modification of naphthoquinones improves their pharmacological properties by introducing amines, amino acids, furan, pyran, pyrazole, triazole, indole, among other chemical groups. In this systematic review, we summarized the preparation of nitrogen naphthoquinones derivatives and discussed their biological effect associated with redox properties and other mechanisms. Preclinical evaluation of antibacterial and/or antitumoral naphthoquinones derivatives is included because cancer is a worldwide health problem, and there is a lack of effective drugs against multidrug-resistant bacteria. The information presented herein indicates that naphthoquinone derivatives could be considered for further studies to provide drugs efficient in treating cancer and multidrug-resistant bacteria.

2 April 2013 in Journal of the American Chemical Society
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Journal Article
Closed access
Denisse de LoeraDenisse de Loera
Denisse de Loera
ASAntoine Stopin
Antoine Stopin
MGMiguel A. Garcia-Garibay
Miguel A. Garcia-Garibay

13 July 2012 in Organic Letters
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Journal Article
Closed access
Denisse de LoeraDenisse de Loera
Denisse de Loera
MGMiguel A. Garcia-Garibay
Miguel A. Garcia-Garibay

20 May 2019 in Synthetic Communications
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Journal Article
Closed access
CACesia M. Aguilar-Morales
Cesia M. Aguilar-Morales
Denisse de LoeraDenisse de Loera
Denisse de Loera
CCClaudia Contreras-Celedón
Claudia Contreras-Celedón
CCCarlos J. Cortés-García
Carlos J. Cortés-García
LCLuis Chacón-García
Luis Chacón-García
A new synthetic strategy to obtain new linked 1,5-disubstituted tetrazole-1,2,3-triazoles via the Ugi-azide reaction followed by a copper-catalyzed alkyne-azide reaction (CuAAC) was developed. This strategy used solvent-free conditions for the Ugi-azide reaction. This two-step strategy affords the products in moderate to good yields. To the best of our knowledge, this is the first report using the CuAAC reaction as a post-condensation process in an Ugi-azide reaction and therefore, the first describing the synthesis of 1,5-disubstituted tetrazole (1,5-DS-T) linked to the 1,2,3-triazole moiety, which are molecules that may have potential applications in medicinal chemistry.

13 June 2018
Verified
Book Chapter
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AIDE SAENZ-GALINDOAIDE SAENZ-GALINDO
AIDE SAENZ-GALINDO
LLLluvia I. López
Lluvia I. López
FCFabiola N. De La Cruz
Fabiola N. De La Cruz
ACAdali Oliva Castañeda-Facio
Adali Oliva Castañeda-Facio
LRLeticia A. Rámirez-Mendoza
Leticia A. Rámirez-Mendoza
Denisse de LoeraDenisse de Loera
Denisse de Loera
Carboxylic acids are versatile organic compounds. In this chapter is presented a current overview of the use of carboxylic acids in a different area as organic synthesis, nanotechnology, and polymers. The application carboxylic acids in these areas are: obtaining of small molecules, macromolecules, synthetic or natural polymers, modification surface of nanoparticles metallic, modification surface of nanostructure such as carbon nanotubes and graphene, nanomaterials, medical field, pharmacy, etc. Carboxylic acids can be natural and synthetic, can be extracted or synthesized, presented chemical structure highly polar, active in organic reactions, as substitution, elimination, oxidation, coupling, etc. In nanotechnology, the use of acid carboxylic as surface modifiers to promote the dispersion and incorporation of metallic nanoparticles or carbon nanostructure, in the area of polymer carboxylic acids present applications such monomers, additives, catalysts, etc. The purpose of this chapter is to emphasize the importance of carboxylic acids in different areas, highlighting the area of organic synthesis, nanotechnology and polymers and its applications.

25 November 2019 in Molecules
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Journal Article
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ERERNESTO RIVERA-AVALOS
ERNESTO RIVERA-AVALOS
Denisse de LoeraDenisse de Loera
Denisse de Loera
JAJorge Gustavo Araujo-Huitrado
Jorge Gustavo Araujo-Huitrado
IEIsmailia Escalante-Garcia
Ismailia Escalante-Garcia
MSMiguel Antonio Muñoz Sánchez
Miguel Antonio Muñoz Sánchez
LLLluvia I. López
Lluvia I. López
We performed an extensive analysis about the reaction conditions of the 1,4-Michael addition of amino acids to 1,4-naphthoquinone and substitution to 2,3-dichloronaphthoquinone, and a complete evaluation of stoichiometry, use of different bases, and the pH influence was performed. We were able to show that microwave-assisted synthesis is the best method for the synthesis of naphthoquinone–amino acid and chloride–naphthoquinone–amino acid derivatives with 79–91% and 78–91% yields, respectively. The cyclic voltammetry profiles showed that both series of naphthoquinone–amino acid derivatives mainly display one quasi-reversible redox reaction process. Interestingly, it was shown that naphthoquinone derivatives possess a selective antitumorigenic activity against cervix cancer cell lines and chloride–naphthoquinone–amino acid derivatives against breast cancer cell lines. Furthermore, the newly synthetized compounds with asparagine–naphthoquinones (3e and 4e) inhibited ~85% of SiHa cell proliferation. These results show promising compounds for specific cervical and breast cancer treatment.