Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vinícius Bonatto"'
Autor:
Vinícius Bonatto, Rafael F. Lameiro, Fernanda R. Rocho, Jerônimo Lameira, Andrei Leitão, Carlos A. Montanari
Publikováno v:
RSC Medicinal Chemistry. 14:201-217
This review highlights the roles of nitriles in covalent inhibitors, their reactivity, examples of pharmaceuticals containing the cyano group and recent developments of nitrile-based inhibitors.
Autor:
Jerônimo Lameira, Clauber Henrique Souza da Costa, Alberto Monteiro dos Santos, Carlos A. Montanari, Vinícius Bonatto, Andrei Leitão
Publikováno v:
Journal of Chemical Information and Modeling. 60:880-889
One tactic for cysteine protease inhibition is to form a covalent bond between an electrophilic atom of the inhibitor and the thiol of the catalytic cysteine. In this study, we evaluate the reaction free energy obtained from a hybrid quantum mechanic
Autor:
Fernanda R. Rocho, Vinícius Bonatto, Rafael F. Lameiro, Jerônimo Lameira, Andrei Leitão, Carlos A. Montanari
Publikováno v:
Expert opinion on therapeutic patents. 32(5)
Cathepsin K (CatK) is a lysosomal cysteine protease and the predominant cathepsin expressed in osteoclasts, where it degrades the bone matrix. Hence, CatK is an attractive therapeutic target related to diseases characterized by bone resorption, like
Autor:
Fernanda dos Reis Rocho, Jerônimo Lameira, Carlos A. Montanari, Andrei Leitão, Vinícius Bonatto, Anwar Shamim, F. Javier Luque
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Covalent inhibitors are assuming central importance in drug discovery projects, especially in this pandemic scenario. Many research groups have focused their attention on inhibiting viral proteases or human proteases such as cathepsin L (hCatL). The
Autor:
Carlos A. Montanari, Sérgio de Albuquerque, Daiane Y. Tezuka, Daniel G. Silva, Caio Haddad Franco, Daniela De Vita, Andrei Leitão, Carolina B. Moraes, Jerônimo Lameira, Pedro Henrique Jatai Batista, Rodrigo Cedron, Vinícius Bonatto, Lorenzo Cianni
Publikováno v:
RSC Med Chem
The cysteine protease cruzipain is considered to be a validated target for therapeutic intervention in the treatment of Chagas disease. Hence, peptidomimetic cruzipain inhibitors having a reactive group (known as warhead) are subject to continuous st
Autor:
Carlos A. Montanari, Jerônimo Lameira, Felipe Cardoso Prado Martins, Vinícius Bonatto, Fernanda dos Reis Rocho, Andrei Leitão, Lorenzo Cianni, Anwar Shamim
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Human cathepsin B (CatB) is an important biological target in cancer therapy. In this work, we performed a knowledge-based design approach and the synthesis of a new set of 19 peptide-like nitrile-based cathepsin inhibitors. Reported compounds were a
Autor:
Carlos A. Montanari, Lorenzo Cianni, Anwar Shamim, Jerônimo Lameira, Fabiana Rosini, Andrei Leitão, Fernanda dos Reis Rocho, Jean F. R. Ribeiro, Vinícius Bonatto
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Cysteine proteases (CPs) are involved in a myriad of actions that include not only protein degradation, but also play an essential biological role in infectious and systemic diseases such as cancer. CPs also act as biomarkers and can be reached by ac