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Dissertação (Mestrado)
Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) e próstata (PC-3 e DU 145) (2019)
Valdes, Talita Alvarenga; Leitão, Andrei (Orientador)
Unidade: Interunidades em Bioengenharia
Subjects: NEOPLASIAS MAMÁRIAS, NEOPLASIAS HEPÁTICAS, NEOPLASIAS PROSTÁTICAS, TERAPIA COMBINADA
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VALDES, Talita Alvarenga. Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) e próstata (PC-3 e DU 145). 2019. Dissertação (Mestrado) – Universidade de São Paulo, São Carlos, 2019. Disponível em: https://www.teses.usp.br/teses/disponiveis/82/82131/tde-27022020-105427/. Acesso em: 08 out. 2025.
APA
Valdes, T. A. (2019). Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) e próstata (PC-3 e DU 145) (Dissertação (Mestrado). Universidade de São Paulo, São Carlos. Recuperado de https://www.teses.usp.br/teses/disponiveis/82/82131/tde-27022020-105427/
NLM
Valdes TA. Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) e próstata (PC-3 e DU 145) [Internet]. 2019 ;[citado 2025 out. 08 ] Available from: https://www.teses.usp.br/teses/disponiveis/82/82131/tde-27022020-105427/
Vancouver
Valdes TA. Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) e próstata (PC-3 e DU 145) [Internet]. 2019 ;[citado 2025 out. 08 ] Available from: https://www.teses.usp.br/teses/disponiveis/82/82131/tde-27022020-105427/
Trabalho de evento-resumo
Synthesis of Covalent Reversible Inhibitors of Cysteine Protease CPB (2019)
Matos, Thiago Kelvin Brito; Leitão, Andrei
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, QUÍMICA MÉDICA
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MATOS, Thiago Kelvin Brito e LEITÃO, Andrei. Synthesis of Covalent Reversible Inhibitors of Cysteine Protease CPB. 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: 08 out. 2025.
APA
Matos, T. K. B., & Leitão, A. (2019). Synthesis of Covalent Reversible Inhibitors of Cysteine Protease CPB. 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
Matos TKB, Leitão A. Synthesis of Covalent Reversible Inhibitors of Cysteine Protease CPB [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Matos TKB, Leitão A. Synthesis of Covalent Reversible Inhibitors of Cysteine Protease CPB [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi.org/10.1021/acsinfecdis.8b00284
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi.org/10.1371/journal.pone.0222055
Artigo de periodico
Characterization, solubility and biological activity of amphihilic biopolymeric Schiff bases synthesized using chitosans (2019)
Barbosa, Hellen Franciane Gonçalves; Attjioui, Maha; Leitão, Andrei ; Moerschbacher, Bruno M; Cavalheiro, Eder Tadeu Gomes
Source: Carbohydrate Polymers. Unidade: IQSC
Assunto: QUITOSANA
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BARBOSA, Hellen Franciane Gonçalves et al. Characterization, solubility and biological activity of amphihilic biopolymeric Schiff bases synthesized using chitosans. Carbohydrate Polymers, v. 220, p. 1-11, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2019.05.037. Acesso em: 08 out. 2025.
APA
Barbosa, H. F. G., Attjioui, M., Leitão, A., Moerschbacher, B. M., & Cavalheiro, E. T. G. (2019). Characterization, solubility and biological activity of amphihilic biopolymeric Schiff bases synthesized using chitosans. Carbohydrate Polymers, 220, 1-11. doi:10.1016/j.carbpol.2019.05.037
NLM
Barbosa HFG, Attjioui M, Leitão A, Moerschbacher BM, Cavalheiro ETG. Characterization, solubility and biological activity of amphihilic biopolymeric Schiff bases synthesized using chitosans [Internet]. Carbohydrate Polymers. 2019 ; 220 1-11.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.carbpol.2019.05.037
Vancouver
Barbosa HFG, Attjioui M, Leitão A, Moerschbacher BM, Cavalheiro ETG. Characterization, solubility and biological activity of amphihilic biopolymeric Schiff bases synthesized using chitosans [Internet]. Carbohydrate Polymers. 2019 ; 220 1-11.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.carbpol.2019.05.037
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi.org/10.1039/c9ra07161j
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] 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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi.org/10.1016/j.bmc.2019.115083
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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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi.org/10.1016/j.exppara.2019.04.001
Trabalho de evento-resumo
Development and validation of an analytical method for the quantification of a dipeptidyl nitrile in the extracellular medium using HPLC-UV (2019)
Batista, Pedro Henrique Jatai; Leitão, Andrei
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: QUÍMICA ANALÍTICA, DOENÇAS PARASITÁRIAS
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ABNT
BATISTA, Pedro Henrique Jatai e LEITÃO, Andrei. Development and validation of an analytical method for the quantification of a dipeptidyl nitrile in the extracellular medium using HPLC-UV. 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: 08 out. 2025.
APA
Batista, P. H. J., & Leitão, A. (2019). Development and validation of an analytical method for the quantification of a dipeptidyl nitrile in the extracellular medium using HPLC-UV. 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
Batista PHJ, Leitão A. Development and validation of an analytical method for the quantification of a dipeptidyl nitrile in the extracellular medium using HPLC-UV [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Batista PHJ, Leitão A. Development and validation of an analytical method for the quantification of a dipeptidyl nitrile in the extracellular medium using HPLC-UV [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1039/C9CP04820K
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
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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: 08 out. 2025.
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 2025 out. 08 ] 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 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Targeting the Shc-EGFR interaction with indomethacin inhibits MAP kinase pathway signalling (2019)
Lin, Chi-Chuan; Suen,Kin Man; Stainthorp,Amy; Wieteska,Lukasz; Biggs,George S.; Leitão, Andrei ; Montanari, Carlos Alberto ; Ladbury, John E.,
Source: Cancer Letters. Unidade: IQSC
Assunto: NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIN, Chi-Chuan et al. Targeting the Shc-EGFR interaction with indomethacin inhibits MAP kinase pathway signalling. Cancer Letters, v. 457, p. 86-97, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.canlet.2019.05.008. Acesso em: 08 out. 2025.
APA
Lin, C. -C., Suen, K. M., Stainthorp, A., Wieteska, L., Biggs, G. S., Leitão, A., et al. (2019). Targeting the Shc-EGFR interaction with indomethacin inhibits MAP kinase pathway signalling. Cancer Letters, 457, 86-97. doi:10.1016/j.canlet.2019.05.008
NLM
Lin C-C, Suen KM, Stainthorp A, Wieteska L, Biggs GS, Leitão A, Montanari CA, Ladbury JE. Targeting the Shc-EGFR interaction with indomethacin inhibits MAP kinase pathway signalling [Internet]. Cancer Letters. 2019 ;457 86-97.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.canlet.2019.05.008
Vancouver
Lin C-C, Suen KM, Stainthorp A, Wieteska L, Biggs GS, Leitão A, Montanari CA, Ladbury JE. Targeting the Shc-EGFR interaction with indomethacin inhibits MAP kinase pathway signalling [Internet]. Cancer Letters. 2019 ;457 86-97.[citado 2025 out. 08 ] Available from: https://doi.org/10.1016/j.canlet.2019.05.008
Trabalho de evento-resumo
Structure-activity relationship using cell-based assay for dipeptidyl nitriles in MIA PaCa-2 pancreatic cancer cells (2019)
Botelho, Sabrina Mendes; Leitão, Andrei
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS, PÂNCREAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOTELHO, Sabrina Mendes e LEITÃO, Andrei. Structure-activity relationship using cell-based assay for dipeptidyl nitriles in MIA PaCa-2 pancreatic cancer cells. 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: 08 out. 2025.
APA
Botelho, S. M., & Leitão, A. (2019). Structure-activity relationship using cell-based assay for dipeptidyl nitriles in MIA PaCa-2 pancreatic cancer cells. 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
Botelho SM, Leitão A. Structure-activity relationship using cell-based assay for dipeptidyl nitriles in MIA PaCa-2 pancreatic cancer cells [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Botelho SM, Leitão A. Structure-activity relationship using cell-based assay for dipeptidyl nitriles in MIA PaCa-2 pancreatic cancer cells [Internet]. Book of Abstracts. 2019 ;[citado 2025 out. 08 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf

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