Now showing items 4655-4674 of 4842

    • Atria Salas, Ana María; Corsini, Gino; González, Lissette; Garland, María Teresa; Baggio, Ricardo (WILEY-BLACKWELL PUBLISHING, 2009-07)
      catena-Poly[[tetraaquabis(1H-pyrazole-kappa N-2) nickel(II)] [[diaquabis(1H-pyrazole-kappa N-2) nickel(II)]-mu-benzene-1,2,4,5-tetracarboxylato-kappa O-2(1):O-4] tetrahydrate], {[Ni(C3H4N2)(2)(H2O)(4)][Ni(C10H2O8)(C3H4N2 ...
    • Moreno, Yanko; Hermosilla, Patricio; Garland, María Teresa; Peña, Octavio; Baggio, Ricardo (2007)
      Two polymorphic forms of a mixed zinc/copper biquinoline dihydrogenphosphate are presented, showing almost identical monomeric units, viz. (2,2 '-biquinoline-kappa N-2,N ')bis(dihydrogenphosphato-kappa O)copper(II)/zinc(II), ...
    • Blondel, Carlos J.; Jiménez, Juan C.; Leiva, Lorenzo E.; Álvarez Armijo, Sergio Aníbal; Pinto, Bernardo I.; Contreras, Francisca; Pezoa, David; Santiviago Cid, Carlos; Contreras, Inés (American Society for Microbiology, 2013-04)
      Salmonella enterica serotype Gallinarum is the causative agent of fowl typhoid, a disease characterized by high morbidity and mortality that causes major economic losses in poultry production. We have reported that S. ...
    • Pezoa, David; Yang, Hee Jeong; Blondel, Carlos J.; Santiviago Cid, Carlos; Andrews Polymenis, Helene L.; Contreras, Inés (PLOS ONE, 2013)
      The role of the Salmonella Pathogenicity Islands (SPIs) in pathogenesis of Salmonella enterica Typhimurium infection in the chicken is poorly studied, while many studies have been completed in murine models. The Type VI ...
    • Jiménez-González, Andrea; Quispe, Cristina; Bórquez, Jorge; Sepúlveda, Beatriz; Riveros, Felipe; Areche, Carlos; Nagles, Edgar; García Beltrán, Olimpo; Simirgiotis, Mario J. (Taylor & Francis, 2018)
      UHPLC/ESI/MS identification of organic compounds is the first step in the majority of screening techniques for the characterization of biologically active metabolites in natural sources. This paper describes a method for ...
    • Fernández Galleguillos, Carlos; Quesada Romero, Luisa; Puerta, Adrián; Padrón, José M.; Souza, Ernane; Romero Parra, Javier Hernán; Simirgiotis, Mario J. (MDPI, 2021)
      Gaultheria pumila (Ericaceae) (known as Chaura or Mutilla) is a Chilean native small shrub that produces berry fruits consumed by local Mapuche people. In this study, the chemical fingerprinting and antioxidant, enzyme ...
    • Becerra Herrera, Mercedes; Honda, Luis; Richter Duk, Pablo (Elsevier, 2015)
      A novel analytical approach involving an improved rotating-disk sorptive extraction (ROSE) procedure and ultra-high-performance liquid chromatography (UHPLC) coupled to an ultraspray electrospray ionization source (UESI) ...
    • Richter Duk, Pablo; Jiménez, Marcela; Salazar, Ricardo; Maricán Riquelme, Adolfo Andrés (ELSEVIER, 2006-11-03)
      In the present work the efficiency of extraction of aliphatic diesel range organics (DROs) and polycyclic aromatic hydrocarbons (PAHs) from soil was assessed by using dynamic modes of pressurized solvent extraction (PSE), ...
    • Soto Delgado, Jorge; Domingo, L. R.; Araya Maturana, Ramiro; Contreras Ramos, Renato (JOHN WILEY & SONS LTD, 2009-06)
      The polar Diels-Alder (DA) reactions of 2-acetyl-1,4-benzoquinone (acBQ) with methyl substituted 1,3-butadienes have been studied using DFT methods at the B3LYP/6-31 G(d) level of theory. These reactions are characterized ...
    • Préndez Bolívar, María Margarita; Ortíz, Jorge; Garrido, Jorge; Huerta P., R.; Alvarez B., C.; Zolezzi Carvallo, Santiago (Akadémiai Kiadó, 1982)
      A simple and rapid method for the multielement routine analysis of atmospheric particulate matter is described. The samples collected on four different types of filters were treated with HNO3 and HCl at 110-120 ºC in pyrex ...
    • Argüello da Silva, Jacqueline; Barría, Claudio Saitz; Jullian Matthaei, Carolina; Navarrete, Patricio; Núñez Vergara, Luis; Squella Serrano, Juan (2005)
      1,4-dihydropyridine derivatives constitute an important pharmacological group for the treatment of cardiovascular diseases. We have synthesised a series 4-(5′-nitro-2′-furyl)-1,4-dihydropyridine derivatives, which were ...
    • Da Silva, Jaqueline; Barría, Claudio; Jullian Matthaei, Carolina; Navarrete Encina, Patricio; Núñez Vergara, Luis; Squella Serrano, Juan (SOC BRASILEIRA QUIMICA, 2005-01)
      1,4-dihydropyridine derivatives constitute an important pharmacological group for the treatment of cardiovascular diseases. We have synthesised a series 4-(5'-nitro-2'-furyl)-1,4-dihydropyridine derivatives, which were ...
    • Fuente, J. de la; Jullian Matthaei, Carolina; Saitz Barría, Claudio; Neira Pacheco, Verónica Alejandra; Poblete, Oscar.; Sobarzo Sánchez, Eduardo (AMER CHEMICAL SOC, 2005-10-28)
      Photoreduction of oxoisoaporphine dyes occurs via a stepwise mechanism of electron-protonelectron transfer that leads to the N-hydrogen oxoisoaporphine anion. When triethylamine, TEA, was used as the electron donor in ...
    • Fuente, Julio R. De la; Cañete, Álvaro; Jullian Matthaei, Carolina; Saitz Barría, Claudio; Aliaga, Christian (The American Society of Photobiology, 2013)
      Photoinduced electron transfer between N-phenylglycine (NPG) and electronically excited triplets of 7-substituted-3- methyl-quinoxalin-2-ones in acetonitrile generate the respective ion radical pair, where by decarboxylation ...
    • Moreno Da Costa, David; Borja, Luis; Verdugo, Camilo; Martinez, Javier; Quintero, Celso; Jaque, Pablo; Trofymchuk, Oleksandra S.; Daniliuc, Constantin G.; Cabrera, Alan R.; Rojas, Rene S. (Royal Society of Chemistry, 2019)
      New 4-amino-3-iminoquinoline derivative ligands (L1-4) were synthesized through an intramolecular exo-dig cyclization of anionic β-diketiminates, containing an N-benzonitrile moiety. The effect of the alkali-metal in this ...
    • Niso Santano, Mireia; Malik, Shoaib; Pietrocola, Federico; Bravo San Pedro, José; Mariño, Guillermo; Cianfanelli, Valentina; Ben-Younès, Amena; Troncoso Cotal, Rodrigo; Markaki, Maria; Sica, Valentina; Izzo, Valentina; Chaba, Kariman; Bauvy, Chantal; Dupont, Nicolas; Kepp, Oliver; Rockenfeller, Patrick; Wolinski, Heimo; Madeo, Frank; Lavandero González, Sergio; Codogno, Patrice; Harper, Francis; Pierron, Gérard; Tavernarakis, Nektarios; Cecconi, Francesco; Maiuri, Maria Chiara; Galluzzi, Lorenzo; Kroemer, Guido (Wiley-Blackwell, 2015)
      To obtain mechanistic insights into the cross talk between lipolysis and autophagy, two key metabolic responses to starvation, we screened the autophagy-inducing potential of a panel of fatty acids in human cancer cells. ...
    • Gómez, Johana; Klahn, A.; Fuentealba, Mauricio; Sierra, Diego; Olea Azar, Claudio; Medina, Manuela (Elsevier, 2015)
      A new series of unsymmetrical cyrhetrenyl and ferrocenyl azines that were monosubstituted [(η5-C5H4)– C(R)_N–N_CH(5-NO2–2-C4H2O)]M {with M_Re(CO)3 and R_H (1a) or R_Me (1b); M_Fe(η5-C5H5) and R_H (2a) or R_Me (2b)} and ...
    • Paredes García, Verónica; Santana, Ricardo C.; Madrid, Rosa; Vega, Andrés; Spodine Spiridonova, Evgenia; Venegas Yazigi, Diego (American Chemical Society, 2013)
      An unusual and unique conformation of a paddle wheel type binuclear copper(II) complex containing acetate and acetamido ligands, {Cu2(μ2-O2CCH3)4}(OCNH2CH3) (1), was obtained by solvothermal synthesis. The structural ...
    • De Bonfils, Paul; Verron, Elise; Sandoval Altamirano, Catalina; Jaque Olmedo, Pablo; Moreau, Xavier; Gunther Sapunar, Germán; Nun, Pierrick; Coeffard, Vincent (Amer Chemical, 2020)
      A series of functionalized 6-alkoxy phenalenones was prepared through an unprecedented oxidative dealkylation of readily available phenalene precursors. The starting phenalenes were efficiently synthesized via an aminocatalyzed ...
    • Cárcamo, J.; Lobos, S.; Merino, A.; Buckbinder, L.; Wienmann, R.; Natarajan, V.; Reinberg, D. (National Institute of Health, 1989)
      Almost every week, it seems, another character appears, expending the cast of DNA-binding proteins. Some of these proteins are destined for major roles, binding to DNA sequences a few hundred basepairs upstream of key ...