Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Omar Gómez-García"'
Publikováno v:
Journal of Fungi, Vol 10, Iss 9, p 629 (2024)
Fungal infections represent a growing public health problem, mainly stemming from two phenomena. Firstly, certain diseases (e.g., AIDS and COVID-19) have emerged that weaken the immune system, leaving patients susceptible to opportunistic pathogens.
Externí odkaz:
https://doaj.org/article/1f88fc29eaaa4b2e915772fd1217e6fc
Autor:
Diter Miranda-Sánchez, Carlos H. Escalante, Dulce Andrade-Pavón, Omar Gómez-García, Edson Barrera, Lourdes Villa-Tanaca, Francisco Delgado, Joaquín Tamariz
Publikováno v:
Molecules, Vol 28, Iss 20, p 7223 (2023)
As a new approach, pyrrolo[1,2-a]pyrazines were synthesized through the cyclization of 2-formylpyrrole-based enaminones in the presence of ammonium acetate. The enaminones were prepared with a straightforward method, reacting the corresponding alkyl
Externí odkaz:
https://doaj.org/article/2c5bef8a35c84402a8917358bbef1760
Autor:
Elizabeth Gómez, José Miguel Galván-Hidalgo, Guillermo Pérez-Cuéllar, Karoline Alondra Huerta-Landa, Arturo González-Hernández, Omar Gómez-García, Dulce Andrade-Pavón, Teresa Ramírez-Apan, Karla Daniela Rodríguez Hernández, Simón Hernández, Patricia Cano-Sánchez, Homero Gómez-Velasco
Publikováno v:
Bioinorganic Chemistry and Applications, Vol 2023 (2023)
Organotin complexes were prepared through a one-pot reaction with three components by reacting thiosemicarbazide or 4-methyl-3-thiosemicarbazide or 4-phenylthiosemicarbazide, dehydroacetic acid (DHA) and dibutyl, diphenyl, dicyclohexyl, and bis[(trim
Externí odkaz:
https://doaj.org/article/73a3634e9eff4e9b9569f8596361de85
Autor:
Dolores G. Aguila-Muñoz, Gabriel Vázquez-Lira, Erika Sarmiento-Tlale, María C. Cruz-López, Fabiola E. Jiménez-Montejo, Víctor E. López y López, Carlos H. Escalante, Dulce Andrade-Pavón, Omar Gómez-García, Joaquín Tamariz, Aarón Mendieta-Moctezuma
Publikováno v:
Molecules, Vol 28, Iss 10, p 4180 (2023)
Current antidiabetic drugs have severe side effects, which may be minimized by new selective molecules that strongly inhibit α-glucosidase and weakly inhibit α-amylase. We have synthesized novel alkoxy-substituted xanthones and imidazole-substitute
Externí odkaz:
https://doaj.org/article/42f2177172c04ace9802ecb32da6b040
Autor:
Alberto Feliciano, Omar Gómez-García, Carlos H. Escalante, Mario A. Rodríguez-Hernández, Mariana Vargas-Fuentes, Dulce Andrade-Pavón, Lourdes Villa-Tanaca, Cecilio Álvarez-Toledano, María Teresa Ramírez-Apan, Miguel A. Vázquez, Joaquín Tamariz, Francisco Delgado
Publikováno v:
Pharmaceuticals, Vol 14, Iss 11, p 1110 (2021)
Chromenes are compounds that may be useful for inhibiting topoisomerase and cytochrome, enzymes involved in the growth of cancer and fungal cells, respectively. The aim of this study was to synthesize a series of some novel 2-amino-3-cyano-4-aryl-6,7
Externí odkaz:
https://doaj.org/article/97b971ae3c79401fb4955520971950c1
Autor:
Omar Gómez-García, Dulce Andrade-Pavón, Elena Campos-Aldrete, Ricardo Ballinas-Indilí, Alfonso Méndez-Tenorio, Lourdes Villa-Tanaca, Cecilio Álvarez-Toledano
Publikováno v:
Molecules, Vol 23, Iss 3, p 599 (2018)
A series of 3-benzoyl imidazo[1,2-a]pyrimidines, obtained from N-heteroarylformamidines in good yields, was tested in silico and in vitro for binding and inhibition of seven Candida species (Candida albicans (ATCC 10231), Candida dubliniensis (CD36),
Externí odkaz:
https://doaj.org/article/1d2d9e25855548df9fa05890cda8274e
Publikováno v:
Indian J Microbiol
Two agents from natural sources, citroflavonoids naringin and naringenin, can target enzymes in pathogenic yeasts responsible for hospital infections and crop failure. The aim of this study was to examine the molecular recognition site for naringin a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3a96c7c06ff38e05af5eb92ba1eec68
https://doi.org/10.1007/s12088-021-00980-0
https://doi.org/10.1007/s12088-021-00980-0
Autor:
DULCE, ANDRADE-PAVÓN1 (AUTHOR) dandradep@ipn.mx, OMAR, GÓMEZ-GARCÍA2 (AUTHOR) jogomezga@ipn.mx, CECILIO, ÁLVAREZ-TOLEDANO3 (AUTHOR)
Publikováno v:
Journal of Chemical Sciences. 2020, Vol. 132 Issue 1, p1-20. 20p.
Autor:
Eva Ramón-Gallegos, Miguel A. Vázquez, Aarón Mendieta, María del Carmen Cruz-López, Catalina Rugerio-Escalona, Abraham Pucheta, Germán Chamorro-Cevallos, Alejandra Ramírez-Villalva, Francisco Delgado, Joaquín Tamariz, Liseth Romero, Fabiola Jiménez, Damian A. Madrigal, Carlos González-Romero, Alfonso Sequeda-Juárez, Omar Gómez-García, Leticia Garduño-Siciliano, Roberto I. Hernández-Benitez, Aydeé Fuentes-Benítes, Lourdes Villa-Tanaca, Blanca Rosales-Acosta, Julio López
Publikováno v:
Medicinal Chemistry Research. 29:459-478
A series of highly potent antihyperlipidemic agents constituted by a fibrate-based structure was recently reported by our group, whose synthesis started from isovanillin derivatives. In the interest of evaluating the bioisosteric effect of the vanill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76107399cbe7003911c6565497181e3f
https://doi.org/10.1007/s00044-019-02496-1
https://doi.org/10.1007/s00044-019-02496-1
Autor:
Dolores G. Aguila-Muñoz, Elizabeth Cervantes-Espinoza, Carlos H. Escalante, Rsuini U. Gutiérrez, María C. Cruz-López, Fabiola E. Jiménez-Montejo, Nemesio Villa-Ruano, Omar Gómez-García, Joaquín Tamariz, Aarón Mendieta-Moctezuma
The aim of the present study was to synthesize isoflavone-enaminones 3a-c and 7-alkoxy-isoflavones 4a-c, evaluate their inhibition of a-glucosidase, and analyze the bioisosteric effect of the presence versus absence of aromatic moieties in these benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1e06cecaa7585c267e99dafaadc2f1a
https://doi.org/10.21203/rs.3.rs-1351698/v1
https://doi.org/10.21203/rs.3.rs-1351698/v1
