Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lucas Lopardi Franco"'
Autor:
Mônica Fraccarolli Pelozo, Giovanna Fiori Serpa Lima, Cleydson Finotti Cordeiro, Luana Sueli Silva, Ivo Santana Caldas, Diogo Teixeira Carvalho, Stefânia Neiva Lavorato, Jamie Anthony Hawkes, Lucas Lopardi Franco
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 24 (2021)
Background: The search for new drug compounds is always challenging and there are several different strategies that involve the most varied and creative approaches in medicinal chemistry. One of them is the technique of molecular hybridisation: formi
Externí odkaz:
https://doaj.org/article/eb100ba8e80c4526913dee02ec9d5d68
Autor:
Ângelo de Fátima, Camila de Paula Pereira, Carolina Raquel Said Dau Gonçalves Olímpio, Breno Germano de Freitas Oliveira, Lucas Lopardi Franco, Pedro Henrique Corrêa da Silva
Publikováno v:
Journal of Advanced Research, Vol 13, Iss , Pp 113-126 (2018)
Schiff bases, an aldehyde- or ketone-like compounds in which the carbonyl group is replaced by an imine or azomethine, are some of the most widely used organic compounds. Indeed, they are widely used for industrial purposes and also exhibit a broad r
Externí odkaz:
https://doaj.org/article/f50162411d3746bca14f7c9aa9b2ac62
Publikováno v:
Orbital: The Electronic Journal of Chemistry, Vol 4, Iss 1, Pp 19-20 (2012)
We report herein the synthesis and characterization of N-acetylglucosamine and D-glucose derivates modified at C-1 for evaluation of antifungal activity as potential hexosaminidases inhibitors. There are various related antifungal commercial drugs, b
Externí odkaz:
https://doaj.org/article/e5cebd2cace946df9cb7ef60142b84c2
Autor:
Lucas Lopardi Franco
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFMGUniversidade Federal de Minas GeraisUFMG.
In Medicinal Chemistry the enzymes of pathogens like fungi or bacteria are considered good molecular targets for the development of new drugs and the inhibition of these enzymes can result in pharmacological action trough the perturbation of metaboli
Externí odkaz:
http://hdl.handle.net/1843/BUBD-A2KGZT
Autor:
Cleydson Finotti Cordeiro, Monica Fraccarolli Pelozo, Stefânia Neiva Lavorato, Luana Sueli Silva, Jamie Anthony Hawkes, Giovanna Fiori Serpa Lima, Lucas Lopardi Franco, Diogo Teixeira Carvalho, Ivo Santana Caldas
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 24 (2021)
Background: The search for new drug compounds is always challenging and there are several different strategies that involve the most varied and creative approaches in medicinal chemistry. One of them is the technique of molecular hybridisation: formi
Autor:
Lucas Lopardi Franco, Jamie Anthony Hawkes, Helloana Azevedo-Barbosa, Danielle Ferreira Dias, Diogo Teixeira Carvalho
Publikováno v:
Mini reviews in medicinal chemistry. 20(19)
Sulfonamides have been in clinical use for many years, and the development of bioactive substances containing the sulfonamide subunit has grown steadily in view of their important biological properties such as antibacterial, antifungal, antiparasitic
Autor:
Guilherme Tadeu Lemos Bastos, Diogo Teixeira Carvalho, Thúlio Wliandon Lemos Barbosa, Luiz Felipe Leomil Coelho, Marcelo Henrique dos Santos, Taciane Maira Magalhães Hipólito, Amanda Latercia Tranches Dias, Thiago Belarmino de Souza, Lucas Lopardi Franco, Ihosvany Rodriguez, Danielle Ferreira Dias
Publikováno v:
LOCUS Repositório Institucional da UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Seventeen new synthetic derivatives of eugenol (6, 8–15 and 8′‐15′) were planned following literature reports on antifungal activities of nitroeugenol and eugenol glucoside. The anti‐Candida activity of these compounds was investigated by i
Autor:
Lucas Lopardi Franco, Pedro Paulo Ribeiro Vieira, Mauro V. de Almeida, Luiz Francisco Rocha e Silva, Adrian Martin Pohlit, Marcelo Siqueira Valle
Publikováno v:
Chemical Biology & Drug Design. 79:790-797
Dihydroperoxides and tetraoxanes derived from symmetrically substituted bis(arylmethyl)acetones were synthesized in modest to good yields using several methods. Three of these compounds exhibit an important in vitro antimalarial activity (1.0 μm ≤
Autor:
Lucas Lopardi, Franco, Mauro Vieira, de Almeida, Luiz Francisco Rocha, E Silva, Pedro Paulo Ribeiro, Vieira, Adrian Martin, Pohlit, Marcelo Siqueira, Valle
Publikováno v:
Chemical biologydrug design. 79(5)
Dihydroperoxides and tetraoxanes derived from symmetrically substituted bis(arylmethyl)acetones were synthesized in modest to good yields using several methods. Three of these compounds exhibit an important in vitro antimalarial activity (1.0 μm ≤
Autor:
Heber Victor Tolomeu
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
As neoplasias estão associadas a um crescimento descontrolado das células, resultante de fatores de risco designados por agentes cancerígenos, sendo uma das maiores causas de morte no mundo. A elevada extensão da doença e a variedade de tumores
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::3d6f67e4f6169137e028f1d4024d0efd