Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Luis M. Ruiz-Perez"'
Autor:
Ian H. Gilbert, Carlos Rodrigues, Marcel Kaiser, Silvia Orenes Lorente, Simon Jones, Luis M. Ruiz Perez, Aura Caldera, Julio A. Urbina, Carmen Jiménez, Reto Brun, Dolores Gonzalez Pacanowska, Wanderley da Souza, Ludovic Gros, Simon Cammerer, Juliany Cola Fernandes Rodrigues
Publikováno v:
Antimicrobial Agents and Chemotherapy. 51:4049-4061
There is an urgent need for the development of new drugs for the treatment of tropical parasitic diseases such as Chagas' disease and leishmaniasis. One potential drug target in the organisms that cause these diseases is sterol biosynthesis. This pap
Autor:
Didier Pez, Dolores Gonzalez Pacanowska, Isabel Leal, Reto Brun, Cyrille Boussard, Fabio Zuccotto, Vanessa Yardley, Luis M. Ruiz Perez, Simon L. Croft, Ian H. Gilbert
Publikováno v:
Bioorganic & Medicinal Chemistry. 11:4693-4711
This paper describes the synthesis of 4'-substituted and 3',4'-disubstituted 5-benzyl-2,4-diaminopyrimidines as selective inhibitors of leishmanial and trypanosomal dihydrofolate reductase. Compounds were then assayed against the recombinant parasite
Autor:
Antonio E. Vidal, Miriam Yagüe-Capilla, Blanca Martínez-Arribas, Daniel García-Caballero, Luis M. Ruiz-Pérez, Dolores González-Pacanowska
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Inosine triphosphate pyrophosphatases (ITPases) are ubiquitous house-cleaning enzymes that specifically recognize deaminated purine nucleotides and catalyze their hydrolytic cleavage. In this work, we have characterized the Trypanosoma bruce
Externí odkaz:
https://doaj.org/article/3983e70babb74e9aa1d7d73fb26957bd
Autor:
Frederick Annang, Guiomar Pérez-Moreno, Caridad Díaz, Victor González-Menéndez, Nuria de Pedro Montejo, José Pérez del Palacio, Paula Sánchez, Scott Tanghe, Ana Rodriguez, Ignacio Pérez-Victoria, Juan Cantizani, Luis M. Ruiz-Pérez, Olga Genilloud, Fernando Reyes, Francisca Vicente, Dolores González-Pacanowska
Publikováno v:
Malaria Journal, Vol 20, Iss 1, Pp 1-10 (2021)
Abstract Background Malaria is a global health problem for which novel therapeutic compounds are needed. To this end, a recently published novel family of antiplasmodial macrolides, strasseriolides A–D, was herein subjected to in vivo efficacy stud
Externí odkaz:
https://doaj.org/article/19452ec86bc944d3bca7f97ac48433c7
Publikováno v:
ChemInform. 30
This paper describes the design and synthesis of potential inhibitors of Trypanosoma cruzi dihydrofolate reductase using a structure-based approach. A model of the structure of the T. cruzi enzyme was compared with the structure of the human enzyme.
Autor:
Juana Carrero-Lérida, Marco Sealey-Cardona, Dolores Gonzalez Pacanowska, Carmen Jiménez-Jiménez, Luis M. Ruiz Perez, Julio A. Urbina
Publikováno v:
Molecular and biochemical parasitology. 160(1)
Trypanosomatids contain predominantly ergostane-based sterols, which differ from cholesterol, the main sterol in mammalian cells, in the presence of a methyl group in the 24 position. The methylation is initiated by S-adenosyl-L-methionine:Delta(24 (
Autor:
Kate de Luca-Fradley, Simon L. Croft, Simon Cammerer, Dolores Gonzalez Pacanowska, Silvia Orenes Lorente, Vanessa Yardley, Carmen Jiménez, Rosario Gómez, Ian H. Gilbert, Julio A. Urbina, Luis M. Ruiz Perez
Publikováno v:
Bioorganicmedicinal chemistry. 13(10)
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluation as inhibitors of squalene synthase in order to explore their potential in the treatment of the parasitic diseases leishmaniasis and Chagas disease
Autor:
Ian H. Gilbert, Dolores González-Pacanowska, Luis M. Ruiz Perez, Didier Pez, Soghra Khabnadideh, Alexander Musso, Reto Brun
Publikováno v:
Bioorganicmedicinal chemistry. 13(7)
This paper describes the design, synthesis and evaluation of a series of 2,4-diaminoquinazolines as inhibitors of leishmanial and trypanosomal dihydrofolate reductase. Compounds were designed by a generating virtual library of compounds and docking t
Autor:
Frederick Boye Annang, Guiomar Pérez-Moreno, Cristina Bosch-Navarrete, Victor González-Menéndez, Jesús Martín, Thomas A. Mackenzie, Maria C. Ramos, Luis M. Ruiz-Pérez, Olga Genilloud, Dolores González-Pacanowska, Francisca Vicente, Fernando Reyes
Publikováno v:
Pharmaceutics, Vol 15, Iss 2, p 492 (2023)
Memnoniella is a fungal genus from which a wide range of diverse biologically active compounds have been isolated. A Memnoniella dichroa CF-080171 extract was identified to exhibit potent activity against Plasmodium falciparum 3D7 and Trypanosoma cru
Externí odkaz:
https://doaj.org/article/2f3f742a6a834001a8f684d3477fc6ba
Publikováno v:
Bioorganicmedicinal chemistry letters. 9(10)
This paper describes the design and synthesis of potential inhibitors of Trypanosoma cruzi dihydrofolate reductase using a structure-based approach. A model of the structure of the T. cruzi enzyme was compared with the structure of the human enzyme.