Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Adrian L. Orjuela"'
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Akademický článek
Synthesis, Characterization, and Preliminary In Vitro Cytotoxic Evaluation of a Series of 2-Substituted Benzo [d] [1,3] Azoles
Autor: Ozvaldo Linares-Anaya, Alcives Avila-Sorrosa, Francisco Díaz-Cedillo, Luis Ángel Gil-Ruiz, José Correa-Basurto, Domingo Salazar-Mendoza, Adrian L. Orjuela, Jorge Alí-Torres, María Teresa Ramírez-Apan, David Morales-Morales
Publikováno v: Molecules, Vol 26, Iss 9, p 2780 (2021)
A series of benzo [d] [1,3] azoles 2-substituted with benzyl- and allyl-sulfanyl groups were synthesized, and their cytotoxic activities were in vitro evaluated against a panel of six human cancer cell lines. The results showed that compounds BTA-1 a
Externí odkaz: https://doaj.org/article/73234c2bf41b4dd293958578f09434e9
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4
Computational Evaluation of Interaction Between Curcumin Derivatives and Amyloid-β Monomers and Fibrils: Relevance to Alzheimer’s Disease
Autor: Randy Mojica-Flores, K.S.J. Rao, Muralidhar L. Hegde, Isaias Lans, Adrian L. Orjuela, Jorge Alí-Torres, Johant Lakey-Beitia
Publikováno v: J Alzheimers Dis
Background: The most important hallmark in the neuropathology of Alzheimer’s disease (AD) is the formation of amyloid-β (Aβ) fibrils due to the misfolding/aggregation of the Aβ peptide. Preventing or reverting the aggregation process has been an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adce4c43dcaefe92fb7e8c097c196df0
https://doi.org/10.3233/jad-200941
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7
Synthesis, Characterization, and Preliminary In Vitro Cytotoxic Evaluation of a Series of 2-Substituted Benzo [d] [1,3] Azoles
Autor: Luis Ángel Gil-Ruiz, Ozvaldo Linares-Anaya, Domingo Salazar-Mendoza, Adrian L. Orjuela, Jorge Alí-Torres, Alcives Avila-Sorrosa, María Teresa Ramírez-Apan, José Correa-Basurto, David Morales-Morales, Francisco Díaz-Cedillo
Publikováno v: Molecules
Volume 26
Issue 9
Molecules, Vol 26, Iss 2780, p 2780 (2021)
A series of benzo [d] [1,3] azoles 2-substituted with benzyl- and allyl-sulfanyl groups were synthesized, and their cytotoxic activities were in vitro evaluated against a panel of six human cancer cell lines. The results showed that compounds BTA-1 a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d1782f925ba23ce766551f347543f8c
https://doi.org/10.3390/molecules26092780
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