Zobrazeno 1 - 10
of 579
pro vyhledávání: '"Peterson, DE"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 208-216 (2022)
Sialic acid is the natural substrate for sialidases and its chemical modification has been a useful approach to generate potent and selective inhibitors. Aiming at advancing the discovery of selective Trypanosoma cruzi trans-sialidase (TcTS) inhibito
Externí odkaz:
https://doaj.org/article/ac9f09de44db475897ef1ba9fc3bbf78
Autor:
Pedro Alves Bezerra Morais, Karolinni B. Britto, Evandro Messias, Peterson de Andrade, Elias Werner, Adilson Vidal Costa, Valdemar Lacerda, Christiano Jorge Gomes Pinheiro, Heberth de Paula, Warley de Souza Borges
Publikováno v:
Journal of Agricultural and Food Chemistry. 71:255-266
Concerned about weed infestation, a major threat to food production and herbicide resistance that interferes in the mechanism of action of the main herbicides, we have synthesized eight isatin derivatives using the "Click Chemistry" approach through
Publikováno v:
STUDIES IN MULTIDISCIPLINARY REVIEW. 3:466-482
A transição escolar é um momento muito importante no desenvolvimento biopsicossocial de toda criança, pois ao sair da pré-escola se depara com uma nova maneira de aprendizagem, de socialização e desenvolvimento, o qual colabora integralmente n
Autor:
Alison Maciel Cezar, Peterson de Pinho, Anny Elise Braga, Camila Cortellete Pereira da Silva, Maurício Cardoso da Silva Junior
Publikováno v:
Aletheia. 55:192-206
Publikováno v:
RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218. 4:e453138
Este artigo tem como objetivo geral a intenção de contribuir com a gestão do conhecimento na Marinha do Brasil (MB). A questão principal que norteou o presente estudo foi: Quais os desafios encontrados pelos usuários do Sistema de Gerência de D
Autor:
Fabrício Figueiró, Ivone Carvalho, Carlos Henrique Tomich de Paula da Silva, Fernando Cidade Torres, Peterson de Andrade, Daniel Fábio Kawano, Joaquín M. Campos, Amanda de Fraga Dias, Ana Maria Oliveira Battastini
Publikováno v:
Future Medicinal Chemistry. 12:689-708
Aim: Glioblastoma multiforme (GBM) is an aggressive cancer with very limited clinical therapies. Herein, we have designed novel mercaptobenzimidazole derivatives (1–7) as multitarget antineoplastic drugs and assessed their antiproliferative profile
Autor:
Maria Giovana Coelho Dias, Vinícius Alves de Oliveira Camargo, Peterson de Souza Giudice, Raissa Araújo Ferreira, Luís Felipe Orsi Gameiro, Fábio Augusto Facio
Publikováno v:
Pesquisa e Clínica em Fisioterapia ISBN: 9786553671904
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21a5754d677dc783888f9ad8aae7d441
https://doi.org/10.37423/220606013
https://doi.org/10.37423/220606013
Autor:
Lara Zahalan, Peterson de Jesus
Publikováno v:
29th International Congress on Waterborne Transportation, Shipbuilding and Offshore Constructions.
Autor:
Sakonwan Kuhaudomlarp, Giulia Pergolizzi, Robert A. Field, Ravindra Pal Singh, Peterson de Andrade, Sergey A. Nepogodiev
Publikováno v:
Chembiochem
Singh, R P, Pergolizzi, G, Nepogodiev, S A, de Andrade, P, Kuhaudomlarp, S & Field, R A 2020, ' Preparative and Kinetic Analysis of β-1,4-and β-1,3-Glucan Phosphorylases Informs Access to Human Milk Oligosaccharide Fragments and Analogues Thereof ', CHEMBIOCHEM, vol. 21, no. 7, pp. 1043-1049 . https://doi.org/10.1002/cbic.201900440
Singh, R P, Pergolizzi, G, Nepogodiev, S A, de Andrade, P, Kuhaudomlarp, S & Field, R A 2020, ' Preparative and Kinetic Analysis of β-1,4-and β-1,3-Glucan Phosphorylases Informs Access to Human Milk Oligosaccharide Fragments and Analogues Thereof ', CHEMBIOCHEM, vol. 21, no. 7, pp. 1043-1049 . https://doi.org/10.1002/cbic.201900440
The enzymatic synthesis of oligosaccharides depends on the availability of suitable enzymes, which remains a limitation. Without recourse to enzyme engineering or evolution approaches, herein we demonstrate the ability of wild‐type cellodextrin pho
Publikováno v:
Beilstein journal of organic chemistry. 18
Sialic acid is the natural substrate for sialidases and its chemical modification has been a useful approach to generate potent and selective inhibitors. Aiming at advancing the discovery of selective