Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ander Francisco Pereira"'
Autor:
Jorge Alberto Valle da Silva, Ander Francisco Pereira, Steven R. LaPlante, Kamil Kuca, Teodorico Castro Ramalho, Tanos Celmar Costa França
Publikováno v:
Biomolecules, Vol 10, Iss 2, p 192 (2020)
In the present work, we performed a complementary quantum mechanical (QM) study to describe the mechanism by which deprotonated pralidoxime (2-PAM) could reactivate human (Homo sapiens sapiens) acetylcholinesterase (HssAChE) inhibited by the nerve ag
Externí odkaz:
https://doaj.org/article/b75a208e14a8474dbfa684f70c30c5a0
Autor:
Teodorico C. Ramalho, Kamil Kuca, Daniel A. Polisel, Daniel H. S. Leal, Elaine F. F. da Cunha, Ander Francisco Pereira, Alexandre A. de Castro, Eugenie Nepovimova, Melissa S. Caetano, Flávia V. Soares
Publikováno v:
Expert Review of Neurotherapeutics. 19:375-395
Alzheimer's disease (AD) is the most common cause of dementia. Clinical progress in this pathogenesis field has drawn the attention of researchers, stimulating the investigation of novel treatment methods. Current therapies that deal with cholinester
Autor:
Elaine F. F. da Cunha, Daiana T. Mancini, Teodorico C. Ramalho, Alexandre A. de Castro, Melissa S. Caetano, Flávia V. Soares, Daniela Rodrigues Silva, Ander Francisco Pereira, Telles Cardoso Silva
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 37:2154-2164
Organophosphorus compounds (OP) nerve agents are among the most toxic chemical substances known. Their toxicity is due to their ability to bind to acetylcholinesterase. Currently, some enzymes, such as phosphotriesterase, human serum paraoxonase 1 an
Publikováno v:
International Journal of Quantum Chemistry. 121
Autor:
Kamil Kuca, Teodorico C. Ramalho, Steven R. LaPlante, Tanos C. C. França, Ander Francisco Pereira, Jorge Alberto Valle da Silva
Publikováno v:
Biomolecules, Vol 10, Iss 2, p 192 (2020)
Biomolecules
Volume 10
Issue 2
Biomolecules
Volume 10
Issue 2
In the present work, we performed a complementary quantum mechanical (QM) study to describe the mechanism by which deprotonated pralidoxime (2-PAM) could reactivate human (Homo sapiens sapiens) acetylcholinesterase (HssAChE) inhibited by the nerve ag
Autor:
Daniel H. S. Leal, Flávia V. Soares, Elaine F. F. da Cunha, Teodorico C. Ramalho, Kamil Kuca, Ander Francisco Pereira, Alexandre A. de Castro
Publikováno v:
Current Alzheimer Research. 15:1161-1178
Introduction: Alzheimer's disease is known to be a chronic disease, with an estimated prevalence of about 10-30%, considering the population over 60 years of age. Most patients with this disorder (> 95%) present the sporadic form, being characterized
Autor:
Flávia V. Soares, Ander Francisco Pereira, Elaine F. F. da Cunha, Daniel H. S. Leal, Daiana T. Mancini, Alexandre A. de Castro, Teodorico C. Ramalho
Publikováno v:
Chemico-biological interactions. 308
Organophosphorus compounds have been widely employed to the development of warfare nerve agents and pesticides, resulting in a huge number of people intoxicated annually, being a serious problem of public health. Efforts worldwide have been done in o
Autor:
Flávia V. Soares, Daniel H. S. Leal, Teodorico C. Ramalho, Daiana T. Mancini, Elaine F. F. da Cunha, Alexandre A. de Castro, Kamil Kuca, Ander Francisco Pereira, Ondrej Krejcar
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 19; Issue 4; Pages: 1257
International Journal of Molecular Sciences, Vol 19, Iss 4, p 1257 (2018)
International Journal of Molecular Sciences; Volume 19; Issue 4; Pages: 1257
International Journal of Molecular Sciences, Vol 19, Iss 4, p 1257 (2018)
Organophosphorus compounds (OP) are part of a group of compounds that may be hazardous to health. They are called neurotoxic agents because of their action on the nervous system, inhibiting the acetylcholinesterase (AChE) enzyme and resulting in a ch