Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Miguel Angel Vilchis-Reyes"'
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:
Irma Cruz Gavilán García, Eva Florencia Lejarazo Gómez, Elvira Santos Santos, Miguel Angel Vilchis-Reyes
Publikováno v:
Journal of Chemical Education. 87:1230-1232
A series of experiments based on problem-solving and collaborative-learning pedagogies are described that encourage students to interpret results and draw conclusions from data. Different approaches including parallel library synthesis, solvent varia
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
Publikováno v:
Formación universitaria v.4 n.1 2011
SciELO Chile
CONICYT Chile
instacron:CONICYT
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Formación Universitaria (Chile) Num.1 Vol.4
SciELO Chile
CONICYT Chile
instacron:CONICYT
Universidad Nacional Autónoma de México
UNAM
Redalyc-UNAM
Formación Universitaria (Chile) Num.1 Vol.4
Resumen Se han disenado una serie de experimentos de laboratorio con el fin de permitir a los alumnos resolver problemas para que a traves del trabajo experimental individual y el trabajo en equipo utilizando las bases de la quimica combinatoria. Se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ddd8bd7475ad1f7c587de8892bae34
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-50062011000100002
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-50062011000100002
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