Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ma. Elena Vargas-Díaz"'
Autor:
Gustavo G. Flores-Bernal, Ma. Elena Vargas-Díaz, Hugo A. Jiménez-Vázquez, Marcos Hernández-Rodríguez, L. Gerardo Zepeda-Vallejo
Publikováno v:
ACS Omega.
Autor:
Anuar, Salazar-Gómez, Ma Elena, Vargas-Díaz, María Estela, Meléndez-Camargo, Saudy Saret, Pablo-Pérez
Publikováno v:
Natural product research. 36(22)
The antinociceptive activity of the ethanolic extract of
Autor:
Gustavo G. Flores-Bernal, Ma. Elena Vargas-Díaz, Daniel Mendoza-Espinosa, Salvador Pérez-Estrada, Joaquín Tamariz, L. Gerardo Zepeda-Vallejo, Julio C. Ontiveros-Rodríguez, Anahí C. Sánchez-Chávez, Alejandro Alvarez-Hernández, Francisco Delgado
Publikováno v:
Tetrahedron Letters. 59:4437-4441
The synthesis and diastereoselective performance of the pseudo C2-symmetric dodecaheterocycle 3 in nucleophilic and electrophilic reactions are reported. Compound 3 proved to be a highly diastereoselective template to generate a pair of enantiomeric
Autor:
Anuar Salazar-Gómez, Ma. Elena Vargas-Díaz, María Estela Meléndez-Camargo, Saudy Saret Pablo-Pérez
The antinociceptive activity of the ethanolic extract of Trixis angustifolia DC. (EETx) was investigated using the acetic acid-induced writhing and the hot-plate tests in mice. In the acetic acid-induced writhing test, mice treated with EETx (50, 100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8543996b65a664188fe51553fa1554bd
Autor:
Julieta Luna-Herrera, Manuel Quintos-Escalante, Anahí C. Sánchez-Chávez, Anuar Salazar-Gómez, L. Gerardo Zepeda-Vallejo, Maria Lourdes Hernández-De Jesús, Ma. Elena Vargas-Díaz
Publikováno v:
Natural Product Research. 33:1477-1481
A phytochemical and antibacterial study of Trixis angustifolia, a species endemic to Mexico, was performed allowing the isolation of six flavones. The minimal inhibitory concentration (MIC) of the hexanic extract, against Mycobacterium tuberculosis H
Autor:
L. Gerardo Zepeda, Francisco Ayala-Mata, M. Jonathan Fragoso-Vázquez, Pedro Joseph-Nathan, Humberto L. Mendoza-Figueroa, Ma. Elena Vargas-Díaz
Publikováno v:
Tetrahedron: Asymmetry. 23:1588-1595
New (1R)-(–)-myrtenal-derived macrocycles 5a and 5b were efficiently used as chiral auxiliaries in the diastereoselective nucleophilic addition of several nucleophiles (RMgX, RLi, LiAlH4, and NaBH4). We observed that the diastereoselectivity depend