Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pedro Azalim"'
Autor:
da Silva, Verônica Diniz, Almeida-Souza, Fernando, Teles, Amanda Mara, Neto, Pedro Azalim, Mondego-Oliveira, Renata, Mendes Filho, Nestor Everton, Taniwaki, Noemi Nosomi, Abreu-Silva, Ana Lucia, Calabrese, Kátia da Silva, Mouchrek Filho, Victor Elias
Publikováno v:
In Industrial Crops & Products 1 September 2018 119:201-208
Autor:
Jéssica Martins de Moura, Valadares, Sumit O, Bajaj, Hongyan, Li, Hua-Yu L, Wang, Simone Cavalcante, Silva, Israel José Pereira, Garcia, Duane Gischewiski, Pereira, Pedro, Azalim, Luis Eduardo Menezes, Quintas, François, Noël, Vanessa Faria, Cortes, George Augustine, O'Doherty, Leandro Augusto, Barbosa
Publikováno v:
J Cell Biochem
Cardiac glycosides, such as digoxin and digitoxin, are compounds that interact with Na(+)/K(+)-ATPase to induce anti-neoplastic effects; however, these cardiac glycosides have narrow therapeutic index. Thus, semi-synthetic analogs of digitoxin with m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0d3943968b495c89865242228b1b4699
https://pubmed.ncbi.nlm.nih.gov/34553411
https://pubmed.ncbi.nlm.nih.gov/34553411
Autor:
Adriana Katz, Fernando M. do Monte, Pedro Azalim, Luis Eduardo M. Quintas, Steven J.D. Karlish, François Noël
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 94:64-72
Introduction Ouabain and digoxin are classical inhibitors of the Na+,K+-ATPase. In addition to their conventional uses as therapeutic agents or experimental tools there is renewed interest due to evidence suggesting they could be endogenous hormones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0bfa2bc133385c95af2908c0a2a8efd
https://doi.org/10.1016/j.vascn.2018.09.001
https://doi.org/10.1016/j.vascn.2018.09.001
Autor:
Verônica Diniz da Silva, Pedro Azalim Neto, Ana Lucia Abreu-Silva, Noemi Nosomi Taniwaki, Nestor Everton Mendes Filho, Fernando Almeida-Souza, Victor Elias Mouchrek Filho, Renata Mondêgo-Oliveira, Amanda Mara Teles, Kátia da Silva Calabrese
Publikováno v:
Industrial Crops and Products. 119:201-208
The complications involved in current leishmaniasis treatment indicate the urgent need for new therapeutic strategies. In research into new compounds from natural products that possess antileishmanial activity, Ocimum canum species from the Brazilian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b7e88059ebf168884e38bb1706e70c6
https://doi.org/10.1016/j.indcrop.2018.04.005
https://doi.org/10.1016/j.indcrop.2018.04.005
Autor:
Pedro, Azalim, Fernando M, do Monte, Mariana Manzano, Rendeiro, Xiaofan, Liu, George A, O'Doherty, Carlos Frederico, Fontes, Suzana Guimarães, Leitão, Luis Eduardo M, Quintas, François, Noël
Publikováno v:
Biochemical pharmacology. 171
There is a renewed interest in the Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60551514935ac6b0bfe6535b7359a13d
https://pubmed.ncbi.nlm.nih.gov/31669257
https://pubmed.ncbi.nlm.nih.gov/31669257
Autor:
François, Noël, Pedro, Azalim, Fernando M, do Monte, Luis Eduardo M, Quintas, Adriana, Katz, Steven J D, Karlish
Publikováno v:
Journal of pharmacological and toxicological methods. 94(Pt 2)
Ouabain and digoxin are classical inhibitors of the NaUsing purified pig kidney NaWe demonstrate unequivocally that for slow binding inhibitors, ouabain and digoxin, long incubation times (≥60 min at 37 °C) are required to avoid under-estimation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28832524cac42be30c4b5e89c10c3995
https://pubmed.ncbi.nlm.nih.gov/30244071
https://pubmed.ncbi.nlm.nih.gov/30244071
Autor:
François Noël, Carlos Frederico Leite Fontes, Xiaofan Liu, Mariana Manzano Rendeiro, Pedro Azalim, Suzana G. Leitão, Fernando M. do Monte, George A. O'Doherty, Luis Eduardo M. Quintas
Publikováno v:
Biochemical Pharmacology. 171:113679
There is a renewed interest in the Na+/K+-ATPase (NKA, EC 3.6.3.9) either as a target for new therapeutic uses or for understanding the putative pathophysiological role of its mammalian endogenous ligands. Recent data indicate that bufalin binds to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe2f4ef9e60008e7d02ba3ffd8e52ef
https://doi.org/10.1016/j.bcp.2019.113679
https://doi.org/10.1016/j.bcp.2019.113679