Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Miguel Angel Martinez‐Urbina"'
Autor:
Miguel Angel Vilchis-Reyes, Luis Roa de la Fuente, Miguel Angel Martinez‐Urbina, Cuauhtemoc Alvarado, Erika M. Ramos-Rivera, José D. Solano, Angeles Dominguez-Rivera
Publikováno v:
Letters in Drug Design & Discovery. 15:1116-1122
Autor:
José D. Soano, Miguel Angel Martinez‐Urbina, Angel Guzman, Eduardo Díaz, Gerardo Hernández, Cuauhtémoc Alvarado, Miguel Angel Vilchis-Reyes
Publikováno v:
Synthetic Communications. 43:993-1006
Synthesis of O-Me ulongamide B and O-Me ulongamide C, modified natural cyclodepsipeptides, was achieved by a convergent route. The respective dipeptides and tridepsipeptides were coupled, obtaining linear depsipentapeptides, which were then deprotect
Autor:
Miguel Angel Martinez‐Urbina, Eduardo Díaz, María Teresa Ramírez Apan, Miguel Angel Vilchis-Reyes, Alejandro Zentella, Angel Guzman, José Luis Ventura Gallegos, Omar Vargas
Publikováno v:
European Journal of Medicinal Chemistry. 45:379-386
A series of 2-methylimidazo[1,2-a]pyridine- and quinoline-substituted 2-aminopyrimidines derivatives were synthesized using a convenient synthetic route. We evaluate the isosteric replacement of methyl groups in 4-(2-methylimidazo[1,2-a]pyridin-3-yl)
Autor:
Marco Cerbón, Eduardo Díaz, Miguel Angel Vilchis-Reyes, Ignacio González-Sánchez, Cuauhtémoc Alvarado, Miguel Angel Martinez‐Urbina, Eduardo Carlos Martínez-Zuñiga, Angel Guzman, Angelina Quintero, José D. Solano
Publikováno v:
European journal of medicinal chemistry. 60
As a part of our research in the chemistry of chalcones we have prepared four pyrimidine monoadducts of bis-chalcones through the reaction with 6-amino-1,3-dimethyl uracil. These compounds displayed cytotoxicity with a massive vacuolation in differen
Autor:
Eduardo Díaz, María Teresa Ramírez Apan, Omar Vargas, Miguel Angel Martinez‐Urbina, Alejandro Zentella, José Luis Ventura Gallegos, Miguel Angel Vilchis-Reyes, Angel Guzman
Publikováno v:
ChemInform. 41
A series of 6-substituted 2-(N-trifluoroacetylamino)imidazopyridines have been synthesized and their bioactivities were evaluated. Compounds 6a, 6c, and 11a were the most active compounds with modest cytotoxic activity against six human cancer cell l
Autor:
Eduardo Díaz, Miguel Angel Martinez‐Urbina, María Teresa Ramírez Apan, Alejandro Zentella, José Luis Ventura Gallegos, Omar Vargas, Miguel Angel Vilchis-Reyes, Angel Guzman
Publikováno v:
European journal of medicinal chemistry. 45(3)
A series of 6-substituted 2-(N-trifluoroacetylamino)imidazopyridines have been synthesized and their bioactivities were evaluated. Compounds 6a, 6c, and 11a were the most active compounds with modest cytotoxic activity against six human cancer cell l