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Artigo de periodico
Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease (2019)
Lopes, Carla Duque ; Possato, Bruna ; Gaspari, Ana Paula Segantin ; Oliveira, Ronaldo Junio ; Abram, Ulrich ; Almeida, José P. A; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Montanari, Carlos Alberto ; Maia, Pedro Ivo da Silva ; Silva, João Santana da ; Albuquerque, Sérgio de ; Carneiro, Zumira Aparecida
Source: ACS Infectious Diseases. Unidades: IQSC, FMRP, FCFRP
Subjects: BIOQUÍMICA, DOENÇA DE CHAGAS
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ABNT
LOPES, Carla Duque et al. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease. ACS Infectious Diseases, v. 5, n. 10, p. 1698-1707, 2019Tradução . . Disponível em: https://doi.org/10.1021/acsinfecdis.8b00284. Acesso em: 03 out. 2024.
APA
Lopes, C. D., Possato, B., Gaspari, A. P. S., Oliveira, R. J., Abram, U., Almeida, J. P. A., et al. (2019). Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease. ACS Infectious Diseases, 5( 10), 1698-1707. doi:10.1021/acsinfecdis.8b00284
NLM
Lopes CD, Possato B, Gaspari APS, Oliveira RJ, Abram U, Almeida JPA, Rocho F dos R, Leitão A, Montanari CA, Maia PI da S, Silva JS da, Albuquerque S de, Carneiro ZA. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease [Internet]. ACS Infectious Diseases. 2019 ; 5( 10): 1698-1707.[citado 2024 out. 03 ] Available from: https://doi.org/10.1021/acsinfecdis.8b00284
Vancouver
Lopes CD, Possato B, Gaspari APS, Oliveira RJ, Abram U, Almeida JPA, Rocho F dos R, Leitão A, Montanari CA, Maia PI da S, Silva JS da, Albuquerque S de, Carneiro ZA. Organometallic Gold(III) complex [Au(Hdamp)(L14)]+ (L1 = SNSDonating Thiosemicarbazone) as a candidate to new formulations against Chagas disease [Internet]. ACS Infectious Diseases. 2019 ; 5( 10): 1698-1707.[citado 2024 out. 03 ] Available from: https://doi.org/10.1021/acsinfecdis.8b00284
Trabalho de evento-resumo
Papain bioreactors as tool for screening cysteine protease ligands (2019)
Leandro, Cleiton Silva; Lopes, Bianca Rebelo; Vieira, Paulo Cezar ; Corrêa, Arlene Gonçalves; Montanari, Carlos Alberto ; Cass, Quezia Bezerra
Source: Livro de Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IQSC
Subjects: QUÍMICA, LIGANTES
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ABNT
LEANDRO, Cleiton Silva et al. Papain bioreactors as tool for screening cysteine protease ligands. 2019, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2019. Disponível em: https://repositorio.usp.br/directbitstream/3ca48f59-6fcb-4f03-830f-e65e3b1776b5/P18315.pdf. Acesso em: 03 out. 2024.
APA
Leandro, C. S., Lopes, B. R., Vieira, P. C., Corrêa, A. G., Montanari, C. A., & Cass, Q. B. (2019). Papain bioreactors as tool for screening cysteine protease ligands. In Livro de Resumos. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de https://repositorio.usp.br/directbitstream/3ca48f59-6fcb-4f03-830f-e65e3b1776b5/P18315.pdf
NLM
Leandro CS, Lopes BR, Vieira PC, Corrêa AG, Montanari CA, Cass QB. Papain bioreactors as tool for screening cysteine protease ligands [Internet]. Livro de Resumos. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/3ca48f59-6fcb-4f03-830f-e65e3b1776b5/P18315.pdf
Vancouver
Leandro CS, Lopes BR, Vieira PC, Corrêa AG, Montanari CA, Cass QB. Papain bioreactors as tool for screening cysteine protease ligands [Internet]. Livro de Resumos. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/3ca48f59-6fcb-4f03-830f-e65e3b1776b5/P18315.pdf
Artigo de periodico
Ligand-induced conformational selection predicts the selectivity of cysteine protease inhibitors (2019)
Sartori, Geraldo Rodrigues ; Leitão, Andrei ; Montanari, Carlos Alberto ; Laughton, Charles A.
Source: PLOS ONE. Unidade: IQSC
Subjects: DOENÇA DE CHAGAS, LIGANTES, PROTEÍNAS
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ABNT
SARTORI, Geraldo Rodrigues et al. Ligand-induced conformational selection predicts the selectivity of cysteine protease inhibitors. PLOS ONE, v. 14, n. 12, p. e0222055, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0222055. Acesso em: 03 out. 2024.
APA
Sartori, G. R., Leitão, A., Montanari, C. A., & Laughton, C. A. (2019). Ligand-induced conformational selection predicts the selectivity of cysteine protease inhibitors. PLOS ONE, 14( 12), e0222055. doi:10.1371/journal.pone.0222055
NLM
Sartori GR, Leitão A, Montanari CA, Laughton CA. Ligand-induced conformational selection predicts the selectivity of cysteine protease inhibitors [Internet]. PLOS ONE. 2019 ; 14( 12): e0222055.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0222055
Vancouver
Sartori GR, Leitão A, Montanari CA, Laughton CA. Ligand-induced conformational selection predicts the selectivity of cysteine protease inhibitors [Internet]. PLOS ONE. 2019 ; 14( 12): e0222055.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0222055
Trabalho de evento-resumo
2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases (2019)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, DOENÇAS PARASITÁRIAS, PEPTÍDEOS
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ABNT
LAMEIRO, Rafael da Fonseca e SHAMIM, Anwar e MONTANARI, Carlos Alberto. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Lameiro, R. da F., Shamim, A., & Montanari, C. A. (2019). 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity? (2019)
Cianni, Lorenzo ; Feldmann, CW; Gilberg, E; Gütschow Michaell; Juliano, Luiz; Leitão, Andrei ; Bajorath, Jurgen; Montanari, Carlos Alberto
Source: Journal of Medicinal Chemistry. Unidade: IQSC
Assunto: NEOPLASIAS
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ABNT
CIANNI, Lorenzo et al. Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity?. Journal of Medicinal Chemistry, v. 62, n. 23, p. 10497-10525 july, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.9b00683. Acesso em: 03 out. 2024.
APA
Cianni, L., Feldmann, C. W., Gilberg, E., Gütschow Michaell,, Juliano, L., Leitão, A., et al. (2019). Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity? Journal of Medicinal Chemistry, 62( 23), 10497-10525 july. doi:10.1021/acs.jmedchem.9b00683
NLM
Cianni L, Feldmann CW, Gilberg E, Gütschow Michaell, Juliano L, Leitão A, Bajorath J, Montanari CA. Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity? [Internet]. Journal of Medicinal Chemistry. 2019 ; 62( 23): 10497-10525 july.[citado 2024 out. 03 ] Available from: https://doi.org/10.1021/acs.jmedchem.9b00683
Vancouver
Cianni L, Feldmann CW, Gilberg E, Gütschow Michaell, Juliano L, Leitão A, Bajorath J, Montanari CA. Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity? [Internet]. Journal of Medicinal Chemistry. 2019 ; 62( 23): 10497-10525 july.[citado 2024 out. 03 ] Available from: https://doi.org/10.1021/acs.jmedchem.9b00683
Trabalho de evento-resumo
Synthesis of peptoids of nitriles as cruzain inhibitors (2019)
Souza, Luana Alves Galvão de; Santos, Deborah Araujo dos; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: DOENÇA DE CHAGAS, QUÍMICA MÉDICA
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ABNT
SOUZA, Luana Alves Galvão de et al. Synthesis of peptoids of nitriles as cruzain inhibitors. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Souza, L. A. G. de, Santos, D. A. dos, Montanari, C. A., & Leitão, A. (2019). Synthesis of peptoids of nitriles as cruzain inhibitors. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Souza LAG de, Santos DA dos, Montanari CA, Leitão A. Synthesis of peptoids of nitriles as cruzain inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Souza LAG de, Santos DA dos, Montanari CA, Leitão A. Synthesis of peptoids of nitriles as cruzain inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells (2019)
Quilles Junior, José Carlos ; Bernardi, Murillo Dorileo Leite; Batista, Pedro Henrique J; Silva, Samelyn da Costa Martins ; Rocha, Camila M.R.; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Anti-Cancer Agents in Medicinal Chemistry. Unidades: IQSC, BIOENGENHARIA
Subjects: NEOPLASIAS, PÂNCREAS, MEDICAMENTO, INIBIÇÃO
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ABNT
QUILLES JUNIOR, José Carlos et al. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells. Anti-Cancer Agents in Medicinal Chemistry, v. 19, p. 112-120, 2019Tradução . . Disponível em: https://doi.org/10.2174/1871520618666181029141649. Acesso em: 03 out. 2024.
APA
Quilles Junior, J. C., Bernardi, M. D. L., Batista, P. H. J., Silva, S. da C. M., Rocha, C. M. R., Montanari, C. A., & Leitão, A. (2019). Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells. Anti-Cancer Agents in Medicinal Chemistry, 19, 112-120. doi:10.2174/1871520618666181029141649
NLM
Quilles Junior JC, Bernardi MDL, Batista PHJ, Silva S da CM, Rocha CMR, Montanari CA, Leitão A. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2019 ; 19 112-120.[citado 2024 out. 03 ] Available from: https://doi.org/10.2174/1871520618666181029141649
Vancouver
Quilles Junior JC, Bernardi MDL, Batista PHJ, Silva S da CM, Rocha CMR, Montanari CA, Leitão A. Biological activity and physicochemical properties of dipeptidyl nitrile derivatives against pancreatic ductal adenocarcinoma cells [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2019 ; 19 112-120.[citado 2024 out. 03 ] Available from: https://doi.org/10.2174/1871520618666181029141649
Trabalho de evento-resumo
Mapping the S1 and S1’ subsites of cysteine proteases for the synthesis of new dipeptidyl nitriles as trypanocidal agents (2019)
Cianni, Lorenzo ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, DOENÇA DE CHAGAS
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ABNT
CIANNI, Lorenzo e MONTANARI, Carlos Alberto. Mapping the S1 and S1’ subsites of cysteine proteases for the synthesis of new dipeptidyl nitriles as trypanocidal agents. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Cianni, L., & Montanari, C. A. (2019). Mapping the S1 and S1’ subsites of cysteine proteases for the synthesis of new dipeptidyl nitriles as trypanocidal agents. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Cianni L, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases for the synthesis of new dipeptidyl nitriles as trypanocidal agents [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Cianni L, Montanari CA. Mapping the S1 and S1’ subsites of cysteine proteases for the synthesis of new dipeptidyl nitriles as trypanocidal agents [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Trabalho de evento-resumo
Análise in vitro da atividade antimetastática e citotóxica de inibidores de cisteíno protease em linhagem de câncer de pâncreas MIA PaCa-2 (2019)
Martins, Heloisa H. Fraga; Leitão, Andrei ; Montanari, Carlos Alberto
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Científica e Tecnológica da Universidade de São Paulo - SIICUSP. Unidades: IQSC, ICMC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS, PÂNCREAS
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ABNT
MARTINS, Heloisa H. Fraga e LEITÃO, Andrei e MONTANARI, Carlos Alberto. Análise in vitro da atividade antimetastática e citotóxica de inibidores de cisteíno protease em linhagem de câncer de pâncreas MIA PaCa-2. 2019, Anais.. São Paulo: Universidade de São Paulo - USP, 2019. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 03 out. 2024.
APA
Martins, H. H. F., Leitão, A., & Montanari, C. A. (2019). Análise in vitro da atividade antimetastática e citotóxica de inibidores de cisteíno protease em linhagem de câncer de pâncreas MIA PaCa-2. In Resumos. São Paulo: Universidade de São Paulo - USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Martins HHF, Leitão A, Montanari CA. Análise in vitro da atividade antimetastática e citotóxica de inibidores de cisteíno protease em linhagem de câncer de pâncreas MIA PaCa-2 [Internet]. Resumos. 2019 ;[citado 2024 out. 03 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Martins HHF, Leitão A, Montanari CA. Análise in vitro da atividade antimetastática e citotóxica de inibidores de cisteíno protease em linhagem de câncer de pâncreas MIA PaCa-2 [Internet]. Resumos. 2019 ;[citado 2024 out. 03 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Artigo de periodico
Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells (2019)
Quilles Junior, José Carlos ; Rocho, Fernanda dos Reis ; Montanari, Carlos Alberto ; Leitão, Andrei ; Mignone, Viviane W.; Arruda, Maria Augusta; Turyanska, Lyudmila ; Bradshaw, Tracey D.
Source: RSC Advances. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS, PÂNCREAS
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ABNT
QUILLES JUNIOR, José Carlos et al. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells. RSC Advances, v. 9, n. 45, p. 36699-36706, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra07161j. Acesso em: 03 out. 2024.
APA
Quilles Junior, J. C., Rocho, F. dos R., Montanari, C. A., Leitão, A., Mignone, V. W., Arruda, M. A., et al. (2019). Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells. RSC Advances, 9( 45), 36699-36706. doi:10.1039/c9ra07161j
NLM
Quilles Junior JC, Rocho F dos R, Montanari CA, Leitão A, Mignone VW, Arruda MA, Turyanska L, Bradshaw TD. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells [Internet]. RSC Advances. 2019 ; 9( 45): 36699-36706.[citado 2024 out. 03 ] Available from: https://doi.org/10.1039/c9ra07161j
Vancouver
Quilles Junior JC, Rocho F dos R, Montanari CA, Leitão A, Mignone VW, Arruda MA, Turyanska L, Bradshaw TD. Apoferritin encapsulation of cysteine protease inhibitors for cathepsin L inhibition in cancer cells [Internet]. RSC Advances. 2019 ; 9( 45): 36699-36706.[citado 2024 out. 03 ] Available from: https://doi.org/10.1039/c9ra07161j
Artigo de periodico
Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes (2019)
Quilles Junior, José C.; Tezuka, Daiane Yukie; Lopes, Carla D; Ribeiro, Fernanda L; Laughton, Charles A; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Experimental Parasitology. Unidades: IQSC, FCFRP
Subjects: PROTOZOA, LEISHMANIA
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ABNT
QUILLES JUNIOR, José C. et al. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes. Experimental Parasitology, v. 200, p. 84-91, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2019.04.001. Acesso em: 03 out. 2024.
APA
Quilles Junior, J. C., Tezuka, D. Y., Lopes, C. D., Ribeiro, F. L., Laughton, C. A., Albuquerque, S. de, et al. (2019). Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes. Experimental Parasitology, 200, 84-91. doi:10.1016/j.exppara.2019.04.001
NLM
Quilles Junior JC, Tezuka DY, Lopes CD, Ribeiro FL, Laughton CA, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes [Internet]. Experimental Parasitology. 2019 ;200 84-91.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.exppara.2019.04.001
Vancouver
Quilles Junior JC, Tezuka DY, Lopes CD, Ribeiro FL, Laughton CA, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives have cytostatic effects against Leishmania spp. promastigotes [Internet]. Experimental Parasitology. 2019 ;200 84-91.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.exppara.2019.04.001
Artigo de periodico
Synthesis and structure-activity relationship of nitrile-based cruzain inhibitors incorporating a trifluoroethylamine-based P2 amide replacement (2019)
Gomes, Juliana C; Cianni, Lorenzo ; Ribeiro, Jean; Rocho, Fernanda dos Reis ; Silva, Samelyn da Costa Martins ; Batista, Pedro Henrique J; Moraes, Carolina Borsoi ; Franco, Caio Haddad ; Freitas Junior, Lúcio H G ; Kenny, Peter W; Leitão, Andrei ; Burtoloso, Antonio Carlos Bender ; Vita, Daniela de; Montanari, Carlos Alberto
Source: Bioorganic and Medicinal Chemistry. Unidades: IQSC, ICB
Assunto: QUÍMICA
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ABNT
GOMES, Juliana C et al. Synthesis and structure-activity relationship of nitrile-based cruzain inhibitors incorporating a trifluoroethylamine-based P2 amide replacement. Bioorganic and Medicinal Chemistry, v. 27, n. 22, p. x 115083, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2019.115083. Acesso em: 03 out. 2024.
APA
Gomes, J. C., Cianni, L., Ribeiro, J., Rocho, F. dos R., Silva, S. da C. M., Batista, P. H. J., et al. (2019). Synthesis and structure-activity relationship of nitrile-based cruzain inhibitors incorporating a trifluoroethylamine-based P2 amide replacement. Bioorganic and Medicinal Chemistry, 27( 22), x 115083. doi:10.1016/j.bmc.2019.115083
NLM
Gomes JC, Cianni L, Ribeiro J, Rocho F dos R, Silva S da CM, Batista PHJ, Moraes CB, Franco CH, Freitas Junior LHG, Kenny PW, Leitão A, Burtoloso ACB, Vita D de, Montanari CA. Synthesis and structure-activity relationship of nitrile-based cruzain inhibitors incorporating a trifluoroethylamine-based P2 amide replacement [Internet]. Bioorganic and Medicinal Chemistry. 2019 ; 27( 22): x 115083.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bmc.2019.115083
Vancouver
Gomes JC, Cianni L, Ribeiro J, Rocho F dos R, Silva S da CM, Batista PHJ, Moraes CB, Franco CH, Freitas Junior LHG, Kenny PW, Leitão A, Burtoloso ACB, Vita D de, Montanari CA. Synthesis and structure-activity relationship of nitrile-based cruzain inhibitors incorporating a trifluoroethylamine-based P2 amide replacement [Internet]. Bioorganic and Medicinal Chemistry. 2019 ; 27( 22): x 115083.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bmc.2019.115083
Artigo de periodico
Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energy (2019)
Lameira, Jerônimo ; Bonatto, Vinícius ; Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Montanari, Carlos Alberto
Source: Physical Chemistry Chemical Physics. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, CINÉTICA QUÍMICA, FÁRMACOS, NEOPLASIAS
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ABNT
LAMEIRA, Jerônimo et al. Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energy. Physical Chemistry Chemical Physics, v. 21, p. 24723-24730, 2019Tradução . . Disponível em: https://doi-org.ez67.periodicos.capes.gov.br/10.1039/C9CP04820K. Acesso em: 03 out. 2024.
APA
Lameira, J., Bonatto, V., Cianni, L., Rocho, F. dos R., Leitão, A., & Montanari, C. A. (2019). Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energy. Physical Chemistry Chemical Physics, 21, 24723-24730. doi:10.1039/c9cp04820k
NLM
Lameira J, Bonatto V, Cianni L, Rocho F dos R, Leitão A, Montanari CA. Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energy [Internet]. Physical Chemistry Chemical Physics. 2019 ; 21 24723-24730.[citado 2024 out. 03 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1039/C9CP04820K
Vancouver
Lameira J, Bonatto V, Cianni L, Rocho F dos R, Leitão A, Montanari CA. Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energy [Internet]. Physical Chemistry Chemical Physics. 2019 ; 21 24723-24730.[citado 2024 out. 03 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1039/C9CP04820K
Trabalho de evento-resumo
Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 (2019)
Santos, Deborah Araujo dos; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE QUÍMICA, QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Deborah Araujo dos e MONTANARI, Carlos Alberto. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Santos, D. A. dos, & Montanari, C. A. (2019). Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Santos DA dos, Montanari CA. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Santos DA dos, Montanari CA. Synthesis of non-peptide nitrile cysteine protease inhibitors with bioisostere sulfonamides at position P3 [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Curadoria
The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem (2019)
Montanari, Carlos Alberto ; Leitão, Andrei ; Lameira, Jerônimo
Unidade: IQSC
Assunto: QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTANARI, Carlos Alberto e LEITÃO, Andrei e LAMEIRA, Jerônimo. The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem. . São Carlos: Universidade de São Paulo, USP, Instituto de Química de São Carlos, IQSC. Disponível em: https://repositorio.usp.br/directbitstream/37ac9284-92ed-40a9-99f9-4de87b9d1874/P18571.pdf. Acesso em: 03 out. 2024. , 2019
APA
Montanari, C. A., Leitão, A., & Lameira, J. (2019). The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem. São Carlos: Universidade de São Paulo, USP, Instituto de Química de São Carlos, IQSC. Recuperado de https://repositorio.usp.br/directbitstream/37ac9284-92ed-40a9-99f9-4de87b9d1874/P18571.pdf
NLM
Montanari CA, Leitão A, Lameira J. The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem [Internet]. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/37ac9284-92ed-40a9-99f9-4de87b9d1874/P18571.pdf
Vancouver
Montanari CA, Leitão A, Lameira J. The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem [Internet]. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/37ac9284-92ed-40a9-99f9-4de87b9d1874/P18571.pdf
Editor de periodico
Chemical Biology and Drug Design (2019)
Selwood, David (Editor); Montanari, Carlos Alberto (Editor)
Source: Chemical Biology and Drug Design. Unidade: IQSC
Subjects: BIOQUÍMICA, BIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/823d6fdb-0e41-4168-8a43-02c997fca1fc/P17911.pdf. Acesso em: 03 out. 2024. , 2019
APA
Chemical Biology and Drug Design. (2019). Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/823d6fdb-0e41-4168-8a43-02c997fca1fc/P17911.pdf
NLM
Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/823d6fdb-0e41-4168-8a43-02c997fca1fc/P17911.pdf
Vancouver
Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2019 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/823d6fdb-0e41-4168-8a43-02c997fca1fc/P17911.pdf
Trabalho de evento-resumo
Predicting the ΔΔGbind of halogenated reversible covalent inhibitors of hCatL through computer simulation (2019)
Lameira, Jerônimo ; Bonatto, Vinícius ; Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAMEIRA, Jerônimo et al. Predicting the ΔΔGbind of halogenated reversible covalent inhibitors of hCatL through computer simulation. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Lameira, J., Bonatto, V., Cianni, L., Rocho, F. dos R., Leitão, A., & Montanari, C. A. (2019). Predicting the ΔΔGbind of halogenated reversible covalent inhibitors of hCatL through computer simulation. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Lameira J, Bonatto V, Cianni L, Rocho F dos R, Leitão A, Montanari CA. Predicting the ΔΔGbind of halogenated reversible covalent inhibitors of hCatL through computer simulation [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Lameira J, Bonatto V, Cianni L, Rocho F dos R, Leitão A, Montanari CA. Predicting the ΔΔGbind of halogenated reversible covalent inhibitors of hCatL through computer simulation [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Trabalho de evento-resumo
How NEQUIMED/IQSC/USP’s using machine learning to aid drug discovery (2019)
Montanari, Carlos Alberto ; Cianni, Lorenzo
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: QUÍMICA, INTELIGÊNCIA ARTIFICIAL, FÁRMACOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTANARI, Carlos Alberto e CIANNI, Lorenzo. How NEQUIMED/IQSC/USP’s using machine learning to aid drug discovery. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Montanari, C. A., & Cianni, L. (2019). How NEQUIMED/IQSC/USP’s using machine learning to aid drug discovery. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Montanari CA, Cianni L. How NEQUIMED/IQSC/USP’s using machine learning to aid drug discovery [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Montanari CA, Cianni L. How NEQUIMED/IQSC/USP’s using machine learning to aid drug discovery [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Trabalho de evento-resumo
Synthesis of novel cysteine protease inhibitors and anti-Trypanosoma cruzi agents (2019)
Martins, Felipe Cardoso Prado; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINS, Felipe Cardoso Prado e MONTANARI, Carlos Alberto. Synthesis of novel cysteine protease inhibitors and anti-Trypanosoma cruzi agents. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Martins, F. C. P., & Montanari, C. A. (2019). Synthesis of novel cysteine protease inhibitors and anti-Trypanosoma cruzi agents. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Martins FCP, Montanari CA. Synthesis of novel cysteine protease inhibitors and anti-Trypanosoma cruzi agents [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Martins FCP, Montanari CA. Synthesis of novel cysteine protease inhibitors and anti-Trypanosoma cruzi agents [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Trabalho de evento-resumo
Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors (2019)
Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Assunto: QUÍMICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHAMIM, Anwar e MONTANARI, Carlos Alberto. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 03 out. 2024.
APA
Shamim, A., & Montanari, C. A. (2019). Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2024 out. 03 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf

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